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1

Multi-component Removal in Flue Gas by Aqua Ammonia  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

component Removal in Flue Gas by Aqua Ammonia component Removal in Flue Gas by Aqua Ammonia Opportunity The Department of Energy's National Energy Technology Laboratory is seeking licensing partners interested in implementing United States Patent Number 7,255,842 entitled "Multi-component Removal in Flue Gas by Aqua Ammonia." This patent discloses a method for the removal of potential environmental-impacting compounds from flue gas streams. The method oxidizes some or all of the acid precursors such as sulfur dioxide (SO 2 ) and nitric oxides (NO x ) into sulfur trioxide and nitrogen dioxide, respectively. Following this step, the gas stream is then treated with aqua ammonia or ammonium hydroxide to capture the compounds via chemical absorption through acid-base or neutralization reactions where a fertilizer is formed.

2

Thief Process Removal of Mercury from Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Process for the Removal of Mercury from Flue Gas Process for the Removal of Mercury from Flue Gas Opportunity The Department of Energy's National Energy Technology Laboratory (NETL) is seeking licensing partners interested in implementing United States Patent Number 6,521,021 entitled "Thief Process for the Removal of Mercury from Flue Gas." Disclosed in this patent is a novel process in which partially combusted coal is removed from the combustion chamber of a power plant using a lance (called a "thief"). This partially combusted coal acts as a thermally activated adsorbent for mercury. When it is in- jected into the duct work of the power plant downstream from the exit port of the combustion chamber, mercury within the flue gas contacts and adsorbs onto the thermally activated sorbent. The sorbent-mercury

3

Thief process for the removal of mercury from flue gas  

DOE Patents [OSTI]

A system and method for removing mercury from the flue gas of a coal-fired power plant is described. Mercury removal is by adsorption onto a thermally activated sorbent produced in-situ at the power plant. To obtain the thermally activated sorbent, a lance (thief) is inserted into a location within the combustion zone of the combustion chamber and extracts a mixture of semi-combusted coal and gas. The semi-combusted coal has adsorptive properties suitable for the removal of elemental and oxidized mercury. The mixture of semi-combusted coal and gas is separated into a stream of gas and semi-combusted coal that has been converted to a stream of thermally activated sorbent. The separated stream of gas is recycled to the combustion chamber. The thermally activated sorbent is injected into the duct work of the power plant at a location downstream from the exit port of the combustion chamber. Mercury within the flue gas contacts and adsorbs onto the thermally activated sorbent. The sorbent-mercury combination is removed from the plant by a particulate collection system.

Pennline, Henry W. (Bethel Park, PA); Granite, Evan J. (Wexford, PA); Freeman, Mark C. (South Park Township, PA); Hargis, Richard A. (Canonsburg, PA); O'Dowd, William J. (Charleroi, PA)

2003-02-18T23:59:59.000Z

4

Multi-component removal in flue gas by aqua ammonia  

DOE Patents [OSTI]

A new method for the removal of environmental compounds from gaseous streams, in particular, flue gas streams. The new method involves first oxidizing some or all of the acid anhydrides contained in the gas stream such as sulfur dioxide (SO.sub.2) and nitric oxide (NO) and nitrous oxide (N.sub.2O) to sulfur trioxide (SO.sub.3) and nitrogen dioxide (NO.sub.2). The gas stream is subsequently treated with aqua ammonia or ammonium hydroxide which captures the compounds via chemical absorption through acid-base or neutralization reactions. The products of the reactions can be collected as slurries, dewatered, and dried for use as fertilizers, or once the slurries have been dewatered, used directly as fertilizers. The ammonium hydroxide can be regenerated and recycled for use via thermal decomposition of ammonium bicarbonate, one of the products formed. There are alternative embodiments which entail stoichiometric scrubbing of nitrogen oxides and sulfur oxides with subsequent separate scrubbing of carbon dioxide.

Yeh, James T. (Bethel Park, PA); Pennline, Henry W. (Bethel Park, PA)

2007-08-14T23:59:59.000Z

5

Enhanced Elemental Mercury Removal from Coal-fired Flue Gas by Sulfur-chlorine Compounds  

E-Print Network [OSTI]

removal from flue gas of coal-fired power plants. Environ.Speciation in a 100-MW Coal-Fired Boiler with Low-NOxControl Technologies for Coal-Fired Power Plants, DOE/NETL

Miller, Nai-Qiang Yan-Zan Qu Yao Chi Shao-Hua Qiao Ray Dod Shih-Ger Chang Charles

2008-01-01T23:59:59.000Z

6

CO2 Removal from Flue Gas Using MIcroporous Metal Organic Frameworks  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Removal from Flue Gas Using Removal from Flue Gas Using Microporous Metal Organic Frameworks Background The mission of the U.S. Department of Energy's (DOE) Existing Plants, Emissions, & Capture (EPEC) Research & Development (R&D) Program is to develop innovative environmental control technologies to enable full use of the nation's vast coal reserves, while at the same time allowing the current fleet of coal-fired power plants to comply with existing and emerging environmental regulations. The EPEC R&D

7

Mercury sorbent delivery system for flue gas  

DOE Patents [OSTI]

The invention presents a device for the removal of elemental mercury from flue gas streams utilizing a layer of activated carbon particles contained within the filter fabric of a filter bag for use in a flue gas scrubbing system.

Klunder; ,Edgar B. (Bethel Park, PA)

2009-02-24T23:59:59.000Z

8

Enhanced Elemental Mercury Removal from Coal-fired Flue Gas by Sulfur-chlorine Compounds  

SciTech Connect (OSTI)

Oxidation of Hg0 with any oxidant or converting it to a particle-bound form can facilitate its removal. Two sulfur-chlorine compounds, sulfur dichloride (SCl2) and sulfur monochloride (S2Cl2), were investigated as oxidants for Hg0 by gas phase reaction and by surface-involved reactions in the presence of flyash or activated carbon. The gas phase reaction rate constants between Hg0 and the sulfur/chlorine compounds were determined, and the effects of temperature and the main components in flue gases were studied. The gas phase reaction between Hg0 and SCl2 is shown to be more rapid than the gas phase reaction with chlorine, and the second order rate constant was 9.1(+-0.5) x 10-18 mL-molecules-1cdots-1 at 373oK. Nitric oxide (NO) inhibited the gas phase reaction of Hg0 with sulfur-chlorine compounds. The presence of flyash or powdered activated carbon in flue gas can substantially accelerate the reaction. The predicted Hg0 removal is about 90percent with 5 ppm SCl2 or S2Cl2 and 40 g/m3 of flyash in flue gas. The combination of activated carbon and sulfur-chlorine compounds is an effective alternative. We estimate that co-injection of 3-5 ppm of SCl2 (or S2Cl2) with 2-3 Lb/MMacf of untreated Darco-KB is comparable in efficiency to the injection of 2-3 Lb/MMacf Darco-Hg-LH. Extrapolation of kinetic results also indicates that 90percent of Hg0 can be removed if 3 Lb/MMacf of Darco-KB pretreated with 3percent of SCl2 or S2Cl2 is used. Unlike gas phase reactions, NO exhibited little effect on Hg0 reactions with SCl2 or S2Cl2 on flyash or activated carbon. Mercuric sulfide was identified as one of the principal products of the Hg0/SCl2 or Hg0/S2Cl2 reactions. Additionally, about 8percent of SCl2 or S2Cl2 in aqueous solutions is converted to sulfide ions, which would precipitate mercuric ion from FGD solution.

Chang, Shih-Ger; Yan, Nai-Qiang; Qu, Zan; Chi, Yao; Qiao, Shao-Hua; Dod, Ray; Chang, Shih-Ger; Miller, Charles

2008-07-02T23:59:59.000Z

9

Final Flue Gas Cleaning (FFGC)  

E-Print Network [OSTI]

Final Flue Gas Cleaning (FFGC) Pilot Plant. The pilot plant (FFGC-PP) will be used to test and evaluate removal of air pollution constituents from the flue gas of a 160 MW, Houston-area power plant operating on 100% petcoke. The two-week long test.... TABLE III FLUE GAS COMPOSITION PETCOKE FIRED POWER PLANT H 2 O 3.2 % O 2 4.9 % CO 2 17.7 % HCl 10 ppm SO 2 6800 ppm SO 3 300 ppm H2SO4 mist 690 ppm NOx 260 ppm...

Stinger, D. H.; Romero, M. H.

2006-01-01T23:59:59.000Z

10

Carbon Dioxide Removal from Flue Gas Using Microporous Metal Organic Frameworks  

SciTech Connect (OSTI)

UOP LLC, a Honeywell Company, in collaboration with Professor Douglas LeVan at Vanderbilt University (VU), Professor Adam Matzger at the University of Michigan (UM), Professor Randall Snurr at Northwestern University (NU), and Professor Stefano Brandani at the University of Edinburgh (UE), supported by Honeywell's Specialty Materials business unit and the Electric Power Research Institute (EPRI), have completed a three-year project to develop novel microporous metal organic frameworks (MOFs) and an associated vacuum-pressure swing adsorption (vPSA) process for the removal of CO{sub 2} from coal-fired power plant flue gas. The project leveraged the team's complementary capabilities: UOP's experience in materials development and manufacturing, adsorption process design and process commercialization; LeVan and Brandani's expertise in high-quality adsorption measurements; Matzger's experience in syntheis of MOFs and the organic components associated with MOFs; Snurr's expertise in molecular and other modeling; Honeywell's expertise in the manufacture of organic chemicals; and, EPRI's knowledge of power-generation technology and markets. The project was successful in that a selective CO{sub 2} adsorbent with good thermal stability and reasonable contaminant tolerance was discovered, and a low cost process for flue gas CO{sub 2} capture process ready to be evaluated further at the pilot scale was proposed. The team made significant progress toward the current DOE post-combustion research targets, as defined in a recent FOA issued by NETL: 90% CO{sub 2} removal with no more than a 35% increase in COE. The team discovered that favorable CO{sub 2} adsorption at more realistic flue gas conditions is dominated by one particular MOF structure type, M/DOBDC, where M designates Zn, Co, Ni, or Mg and DOBDC refers to the form of the organic linker in the resultant MOF structure, dioxybenzenedicarboxylate. The structure of the M/DOBDC MOFs consists of infinite-rod secondary building units bound by DOBDC resulting in 1D hexagonal pores about 11 angstroms in diameter. Surface areas range from 800 to 1500 sq m/g for the different MOFs. Mg/DOBDC outperformed all MOF and zeolite materials evaluated to date, with about 25 wt% CO{sub 2} captured by this MOF at flue gas conditions ({approx}0.13 atm CO{sub 2} pressure, 311K). In simulated flue gas without oxygen, the zero-length (ZLC) system was very useful in quickly simulating the effect of long term exposure to impurities on the MOFs. Detailed adsorption studies on MOF pellets have shown that water does not inhibit CO{sub 2} adsorption for MOFs as much as it does for typical zeolites. Moreover, some MOFs retain a substantial CO{sub 2} capacity even with a modest water loading at room temperature. Molecular modeling was a key activity in three areas of our earlier DOE/NETL-sponsored MOF-based research on CC. First, the team was able to effectively simulate CO{sub 2} and other gas adsorption isotherms for more than 20 MOFs, and the knowledge obtained was used to help predict new MOF structures that should be effective for CO{sub 2} adsorption at low pressure. The team also showed that molecular modeling could be utilized to predict the hydrothermal stability of a given MOF. Finally, the team showed that low moisture level exposure actually enhanced the CO{sub 2} adsorption performance of a particular MOF, HKUST-1.

David A Lesch

2010-06-30T23:59:59.000Z

11

Near-Zero Emissions Oxy-Combustion Flue Gas Purification Task 2: SOx/Nox/Hg Removal for High Sulfur Coal  

SciTech Connect (OSTI)

The goal of this project is to develop a near-zero emissions flue gas purification technology for existing PC (pulverized coal) power plants that are retrofitted with oxy-combustion technology. The objective of Task 2 of this project was to evaluate an alternative method of SOx, NOx and Hg removal from flue gas produced by burning high sulfur coal in oxy-combustion power plants. The goal of the program was not only to investigate a new method of flue gas purification but also to produce useful acid byproduct streams as an alternative to using a traditional FGD and SCR for flue gas processing. During the project two main constraints were identified that limit the ability of the process to achieve project goals. 1) Due to boiler island corrosion issues >60% of the sulfur must be removed in the boiler island with the use of an FGD. 2) A suitable method could not be found to remove NOx from the concentrated sulfuric acid product, which limits sale-ability of the acid, as well as the NOx removal efficiency of the process. Given the complexity and safety issues inherent in the cycle it is concluded that the acid product would not be directly saleable and, in this case, other flue gas purification schemes are better suited for SOx/NOx/Hg control when burning high sulfur coal, e.g. this project's Task 3 process or a traditional FGD and SCR.

Nick Degenstein; Minish Shah; Doughlas Louie

2012-05-01T23:59:59.000Z

12

Impact of additives for enhanced sulfur dioxide removal on re-emissions of mercury in wet flue gas desulfurization  

Science Journals Connector (OSTI)

Abstract The wet flue gas desulfurization process (FGD) in fossil fired power plants offers the advantage of simultaneously removing SO2 and other water soluble pollutants, such as certain oxidized mercury compounds (Hg2+). In order to maximize SO2 removal efficiency of installed FGD units, organic additives can be utilized. In the context of multi-pollutant control by wet FGD, the effect of formic and adipic acid on redox reactions of dissolved mercury compounds is investigated with a continuously operated lab-scale test-rig. For sulfite ( SO 3 2 - ) concentrations above a certain critical value, their potential as reducing agent leads to rapidly increasing formation and re-emission of elemental mercury (Hg0). Increasing chloride concentration and decreasing pH and slurry temperature have been identified as key factors for depressing Hg0 re-emissions. Both organic additives have a negative impact on Hg-retention and cause increased Hg0 re-emissions in the wet FGD process, with formic acid being the significantly stronger reducing agent. Different pathways of Hg2+ reduction were identified by qualitative interpretation of the pH-dependence and by comparison of activation enthalpies and activation entropies. While the first mechanism proposed identifies SO 3 2 - as reducing agent and is therefore relevant for any FGD process, the second mechanism involves the formate anion, thus being exclusively relevant for \\{FGDs\\} utilizing formic acid as additive.

Barna Heidel; Melanie Hilber; Günter Scheffknecht

2014-01-01T23:59:59.000Z

13

Development and Demonstration of Waste Heat Integration with Solvent Process for More Efficient CO2 Removal from Coal-Fired Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

and Demonstration of and Demonstration of Waste Heat Integration with Solvent Process for More Efficient CO 2 Removal from Coal-Fired Flue Gas Background The mission of the U.S. Department of Energy/National Energy Technology Laboratory (DOE/NETL) Existing Plants, Emissions, & Capture (EPEC) Research & Development (R&D) Program is to develop innovative environmental control technologies to enable full use of the nation's vast coal reserves, while at the same time allowing the current fleet of coal-

14

Control of scale in flue gas scrubbers  

SciTech Connect (OSTI)

This patent describes a flue gas desulfurization system in which sulfur dioxide-containing flue gas is passed in countercurrent flow with an aqueous calcium-bearing scrubbing liquor whereby the sulfur dioxide is removed from the flue gas by being absorbed by the scrubbing liquor and converted to calcium sulfite and/or calcium sulfate. The improvement of minimizing the formation of calcium scale on the surfaces of the system comprises maintaining in the scrubbing liquor about 0.1-25 ppm of a 1:1 diisobutylene-maleic anhydride copolymer having an average molecular weight of 11000. The copolymer is incorporated in the scrubbing liquor as a 10-15% aqueous dispersion.

Thomas, P.A.; Dewitt-Dick, D.B.

1987-06-02T23:59:59.000Z

15

Experimental research on emission and removal of dioxins in flue gas from a co-combustion of MSW and coal incinerator  

SciTech Connect (OSTI)

This paper describes the experimental study of dioxins removal from flue gas from a co-combustion municipal solid waste and coal incinerator by means of a fluidized absorption tower and a fabric filter. A test rig has been set up. The flow rate of flue gas of the test rig is 150-2000 m{sup 3}/h. The system was composed of a humidification and cooling system, an absorption tower, a demister, a slurry make-up tank, a desilter, a fabric filter and a measurement system. The total height of the absorption tower was 6.5 m, and the diameter of the reactor pool was 1.2 m. When the absorbent was 1% limestone slurry, the recirculation ratio was 3, the jet rate was 5-15 m/s and the submerged depth of the bubbling pipe under the slurry was 0.14 m, the removal efficiency for dioxins was 99.35%. The concentration of dioxins in the treated flue gas was 0.1573 x 10{sup -13} kg/Nm{sup 3} and the concentration of oxygen was 11%. This concentration is comparable to the emission standards of other developed countries.

Zhong Zhaoping [Department of Power Engineering, Research Institute of Thermal Energy Engineering, Key Laboratory of Clean Coal Power Generation and Combustion Technology of Ministry of Education, Southeast University, Nanjing 210096 (China)]. E-mail: zzhong@seu.edu.cn; Jin Baosheng [Department of Power Engineering, Research Institute of Thermal Energy Engineering, Key Laboratory of Clean Coal Power Generation and Combustion Technology of Ministry of Education, Southeast University, Nanjing 210096 (China); Huang Yaji [Department of Power Engineering, Research Institute of Thermal Energy Engineering, Key Laboratory of Clean Coal Power Generation and Combustion Technology of Ministry of Education, Southeast University, Nanjing 210096 (China); Zhou Hongcang [Department of Power Engineering, Research Institute of Thermal Energy Engineering, Key Laboratory of Clean Coal Power Generation and Combustion Technology of Ministry of Education, Southeast University, Nanjing 210096 (China); Lan Jixiang [Department of Power Engineering, Research Institute of Thermal Energy Engineering, Key Laboratory of Clean Coal Power Generation and Combustion Technology of Ministry of Education, Southeast University, Nanjing 210096 (China)

2006-07-01T23:59:59.000Z

16

Recovery of Water from Boiler Flue Gas  

SciTech Connect (OSTI)

This project dealt with use of condensing heat exchangers to recover water vapor from flue gas at coal-fired power plants. Pilot-scale heat transfer tests were performed to determine the relationship between flue gas moisture concentration, heat exchanger design and operating conditions, and water vapor condensation rate. The tests also determined the extent to which the condensation processes for water and acid vapors in flue gas can be made to occur separately in different heat transfer sections. The results showed flue gas water vapor condensed in the low temperature region of the heat exchanger system, with water capture efficiencies depending strongly on flue gas moisture content, cooling water inlet temperature, heat exchanger design and flue gas and cooling water flow rates. Sulfuric acid vapor condensed in both the high temperature and low temperature regions of the heat transfer apparatus, while hydrochloric and nitric acid vapors condensed with the water vapor in the low temperature region. Measurements made of flue gas mercury concentrations upstream and downstream of the heat exchangers showed a significant reduction in flue gas mercury concentration within the heat exchangers. A theoretical heat and mass transfer model was developed for predicting rates of heat transfer and water vapor condensation and comparisons were made with pilot scale measurements. Analyses were also carried out to estimate how much flue gas moisture it would be practical to recover from boiler flue gas and the magnitude of the heat rate improvements which could be made by recovering sensible and latent heat from flue gas.

Edward Levy; Harun Bilirgen; Kwangkook Jeong; Michael Kessen; Christopher Samuelson; Christopher Whitcombe

2008-09-30T23:59:59.000Z

17

Near-Zero Emissions Oxy-Combustion Flue Gas Purification Task 3: SOx/NOx/Hg Removal for Low Sulfur Coal  

SciTech Connect (OSTI)

The goal of this project was to develop a near-zero emissions flue gas purification technology for existing PC (pulverized coal) power plants that are retrofitted with oxycombustion technology. The objective of Task 3 of this project was to evaluate an alternative method of SOx, NOx and Hg removal from flue gas produced by burning low sulfur coal in oxy-combustion power plants. The goal of the program was to conduct an experimental investigation and to develop a novel process for simultaneously removal of SOx and NOx from power plants that would operate on low sulfur coal without the need for wet-FGD & SCRs. A novel purification process operating at high pressures and ambient temperatures was developed. Activated carbonâ??s catalytic and adsorbent capabilities are used to oxidize the sulfur and nitrous oxides to SO{sub 3} and NO{sub 2} species, which are adsorbed on the activated carbon and removed from the gas phase. Activated carbon is regenerated by water wash followed by drying. The development effort commenced with the screening of commercially available activated carbon materials for their capability to remove SO{sub 2}. A bench-unit operating in batch mode was constructed to conduct an experimental investigation of simultaneous SOx and NOx removal from a simulated oxyfuel flue gas mixture. Optimal operating conditions and the capacity of the activated carbon to remove the contaminants were identified. The process was able to achieve simultaneous SOx and NOx removal in a single step. The removal efficiencies were >99.9% for SOx and >98% for NOx. In the longevity tests performed on a batch unit, the retention capacity could be maintained at high level over 20 cycles. This process was able to effectively remove up to 4000 ppm SOx from the simulated feeds corresponding to oxyfuel flue gas from high sulfur coal plants. A dual bed continuous unit with five times the capacity of the batch unit was constructed to test continuous operation and longevity. Full-automation was implemented to enable continuous operation (24/7) with minimum operator supervision. Continuous run was carried out for 40 days. Very high SOx (>99.9%) and NOx (98%) removal efficiencies were also achieved in a continuous unit. However, the retention capacity of carbon beds for SOx and NOx was decreased from ~20 hours to ~10 hours over a 40 day period of operation, which was in contrast to the results obtained in a batch unit. These contradictory results indicate the need for optimization of adsorption-regeneration cycle to maintain long term activity of activated carbon material at a higher level and thus minimize the capital cost of the system. In summary, the activated carbon process exceeded performance targets for SOx and NOx removal efficiencies and it was found to be suitable for power plants burning both low and high sulfur coals. More efforts are needed to optimize the system performance.

Monica Zanfir; Rahul Solunke; Minish Shah

2012-06-01T23:59:59.000Z

18

Recovery of Water from Boiler Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

RecoveRy of WateR fRom BoileR flue Gas RecoveRy of WateR fRom BoileR flue Gas Background Coal-fired power plants require large volumes of water for efficient operation, primarily for cooling purposes. Public concern over water use is increasing, particularly in water stressed areas of the country. Analyses conducted by the U.S. Department of Energy's National Energy Technology Laboratory predict significant increases in power plant freshwater consumption over the coming years, encouraging the development of technologies to reduce this water loss. Power plant freshwater consumption refers to the quantity of water withdrawn from a water body that is not returned to the source but is lost to evaporation, while water withdrawal refers to the total quantity of water removed from a water source.

19

Flue gas desulfurization/denitrification using metal-chelate additives  

DOE Patents [OSTI]

A method of simultaneously removing SO/sub 2/ and NO from oxygen-containing flue gases resulting from the combustion of carbonaceous material by contacting the flue gas with an aqueous scrubber solution containing an aqueous sulfur dioxide sorbent and an active metal chelating agent which promotes a reaction between dissolved SO/sub 2/ and dissolved NO to form hydroxylamine N-sulfonates. The hydroxylamine sulfonates are then separated from the scrubber solution which is recycled. 3 figs.

Harkness, J.B.L.; Doctor, R.D.; Wingender, R.J.

1985-08-05T23:59:59.000Z

20

natural gas+ condensing flue gas heat recovery+ water creation...  

Open Energy Info (EERE)

natural gas+ condensing flue gas heat recovery+ water creation+ CO2 reduction+ cool exhaust gases+ Energy efficiency+ commercial building energy efficiency+ industrial energy...

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

FIELD TEST PROGRAM FOR LONG-TERM OPERATION OF A COHPAC SYSTEM FOR REMOVING MERCURY FROM COAL-FIRED FLUE GAS  

SciTech Connect (OSTI)

With the Nation's coal-burning utilities facing the possibility of tighter controls on mercury pollutants, the U.S. Department of Energy is funding projects that could offer power plant operators better ways to reduce these emissions at much lower costs. Sorbent injection technology represents one of the simplest and most mature approaches to controlling mercury emissions from coal-fired boilers. It involves injecting a solid material such as powdered activated carbon into the flue gas. The gas-phase mercury in the flue gas contacts the sorbent and attaches to its surface. The sorbent with the mercury attached is then collected by the existing particle control device along with the other solid material, primarily fly ash. During 2001, ADA Environmental Solutions (ADA-ES) conducted a full-scale demonstration of sorbent-based mercury control technology at the Alabama Power E.C. Gaston Station (Wilsonville, AL). This unit burns a low-sulfur bituminous coal and uses a hot-side electrostatic precipitator (ESP) in combination with a Compact Hybrid Particulate Collector (COHPAC{trademark}) baghouse to collect fly ash. The majority of the fly ash is collected in the ESP with the residual being collected in the COHPAC{trademark} baghouse. Activated carbon was injected between the ESP and COHPAC{trademark} units to collect the mercury. Short-term mercury removal levels in excess of 90% were achieved using the COHPAC{trademark} unit. The test also showed that activated carbon was effective in removing both forms of mercury--elemental and oxidized. However, a great deal of additional testing is required to further characterize the capabilities and limitations of this technology relative to use with baghouse systems such as COHPAC{trademark}. It is important to determine performance over an extended period of time to fully assess all operational parameters. The project described in this report focuses on fully demonstrating sorbent injection technology at a coal-fired power generating plant that is equipped with a COHPAC{trademark} system. The overall objective is to evaluate the long-term effects of sorbent injection on mercury capture and COHPAC{trademark} performance. The work is being done on one-half of the gas stream at Alabama Power Company's Plant Gaston Unit 3 (nominally 135 MW). Data from the testing will be used to determine: (1) If sorbent injection into a high air-to-cloth ratio baghouse is a viable, long-term approach for mercury control; and (2) Design criteria and costs for new baghouse/sorbent injection systems that will use a similar, polishing baghouse (TOXECON{trademark}) approach.

Jean Bustard; Charles Lindsey; Paul Brignac; Travis Starns; Sharon Sjostrom; Trent Taylor; Cindy Larson

2004-01-29T23:59:59.000Z

22

Field Test Program for Long-Term Operation of a COHPAC System for Removing Mercury from Coal-Fired Flue Gas  

SciTech Connect (OSTI)

With the Nation's coal-burning utilities facing the possibility of tighter controls on mercury pollutants, the U.S. Department of Energy is funding projects that could offer power plant operators better ways to reduce these emissions at much lower costs. Sorbent injection technology represents one of the simplest and most mature approaches to controlling mercury emissions from coal-fired boilers. It involves injecting a solid material such as powdered activated carbon into the flue gas. The gas-phase mercury in the flue gas contacts the sorbent and attaches to its surface. The sorbent with the mercury attached is then collected by the existing particle control device along with the other solid material, primarily fly ash. During 2001, ADA Environmental Solutions (ADA-ES) conducted a full-scale demonstration of sorbent-based mercury control technology at the Alabama Power E.C. Gaston Station (Wilsonville, Alabama). This unit burns a low-sulfur bituminous coal and uses a hot-side electrostatic precipitator (ESP) in combination with a Compact Hybrid Particulate Collector (COHPAC{reg_sign}) baghouse to collect fly ash. The majority of the fly ash is collected in the ESP with the residual being collected in the COHPAC{reg_sign} baghouse. Activated carbon was injected between the ESP and COHPAC{reg_sign} units to collect the mercury. Short-term mercury removal levels in excess of 90% were achieved using the COHPAC{reg_sign} unit. The test also showed that activated carbon was effective in removing both forms of mercury-elemental and oxidized. However, a great deal of additional testing is required to further characterize the capabilities and limitations of this technology relative to use with baghouse systems such as COHPAC{reg_sign}. It is important to determine performance over an extended period of time to fully assess all operational parameters. The project described in this report focuses on fully demonstrating sorbent injection technology at a coal-fired power generating plant that is equipped with a COHPAC{reg_sign} system. The overall objective is to evaluate the long-term effects of sorbent injection on mercury capture and COHPAC{reg_sign} performance. The work is being done on one-half of the gas stream at Alabama Power Company's Plant Gaston Unit 3 (nominally 135 MW). Data from the testing will be used to determine: (1) If sorbent injection into a high air-to-cloth ratio baghouse is a viable, long-term approach for mercury control; and (2) Design criteria and costs for new baghouse/sorbent injection systems that will use a similar, polishing baghouse (TOXECON{trademark}) approach.

Jean Bustard; Charles Lindsey; Paul Brignac; Travis Starns; Sharon Sjostrom; Trent Taylor; Cindy Larson

2004-06-04T23:59:59.000Z

23

Packed-Bed Reactor Study of NETL Sample 196c for the Removal of Carbon Dioxide from Simulated Flue Gas Mixture  

SciTech Connect (OSTI)

An amine-based solid sorbent process to remove CO2 from flue gas has been investigated. The sorbent consists of polyethylenimine (PEI) immobilized onto silica (SiO2) support. Experiments were conducted in a packed-bed reactor and exit gas composition was monitored using mass spectrometry. The effects of feed gas composition (CO2 and H2O), temperature, and simulated steam regeneration were examined for both the silica support as well as the PEI-based sorbent. The artifact of the empty reactor was also quantified. Sorbent CO2 capacity loading was compared to thermogravimetric (TGA) results to further characterize adsorption isotherms and better define CO2 working capacity. Sorbent stability was monitored by periodically repeating baseline conditions throughout the parametric testing and replacing with fresh sorbent as needed. The concept of the Basic Immobilized Amine Sorbent (BIAS) Process using this sorbent within a system where sorbent continuously flows between the absorber and regenerator was introduced. The basic tenet is to manipulate or control the level of moisture on the sorbent as it travels around the sorbent circulation path between absorption and regeneration stages to minimize its effect on regeneration heat duty.

Hoffman, James S.; Hammache, Sonia; Gray, McMahan L.; Fauth Daniel J.; Pennline, Henry W.

2012-04-24T23:59:59.000Z

24

Hybrid heat exchange for the compression capture of CO2 from recirculated flue gas  

SciTech Connect (OSTI)

An approach proposed for removal of CO2 from flue gas cools and compresses a portion of a recirculated flue-gas stream, condensing its volatile materials for capture. Recirculating the flue gas concentrates SOx, H2O and CO2 while dramatically reducing N2 and NOx, enabling this approach, which uses readily available industrial components. A hybrid system of indirect and direct-contact heat exchange performs heat and mass transfer for pollutant removal and energy recovery. Computer modeling and experimentation combine to investigate the thermodynamics, heat and mass transfer, chemistry and engineering design of this integrated pollutant removal (IPR) system.

Oryshchyn, Danylo B.; Ochs, Thomas L.; Summers, Cathy A.

2004-01-01T23:59:59.000Z

25

Catalysts for Oxidation of Mercury in Flue Gas - Energy Innovation...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

those for selective catalytic reduction (SCR)), scrubbing liquors, flue gas or coal additives, combustion modifications, barrier discharges, and ultraviolet radiation....

26

Commercial demonstration of the NOXSO SO{sub 2}/NO{sub x} removal flue gas cleanup system. Quarterly technical progress report No. 13, March 1, 1994--May 31, 1994  

SciTech Connect (OSTI)

The NOXSO process is a dry, post-combustion flue gas treatment technology which uses a regenerable sorbent to simultaneously adsorb sulfur dioxide (SO{sub 2}) and nitrogen oxides (NO{sub x}) from the flue gas of a coal-fired utility boiler. In the process, the SO{sub 2} is converted to a sulfur by-product and the NO{sub x} is converted to nitrogen and oxygen. It is predicted that the process can economically remove 90% of the acid rain precursor gases from the flue gas stream in a retrofit or new facility. The objective of the NOXSO Demonstration Project is to design, construct, and operate a flue gas treatment system utilizing the NOXSO process. The effectiveness of the process will be demonstrated by achieving significant reductions in emissions of sulfur and nitrogen oxides. In addition, sufficient operating data will be obtained to confirm the process economics and provide a basis to guarantee performance on a commercial scale. The project is presently in the project definition and preliminary design phase. Data obtained during pilot plant testing which was completed on July 30, 1993 is being incorporated in the design of the commercial size plant. A suitable host site to demonstrate the NOXSO process on a commercial scale is presently being sought. Preliminary engineering activities involved evaluating various design options for the major process vessels with the principal focus being on the sorbent heater vessel, which is operated at the highest temperature. Additionally, the impact of the NOXSO system on power plant particulate emissions and opacity was estimated. It is predicted that particulate emissions will decrease slightly while opacity will increase slightly. Neither change will be significant enough to have an impact on emissions compliance. Advertised performance of the proposed adsorber separator is being verified by laboratory testing. Process studies activities included POC equipment inspection and materials evaluations.

NONE

1994-12-31T23:59:59.000Z

27

Carbon Dioxide Capture from Flue Gas Using Dry, Regenerable Sorbents  

SciTech Connect (OSTI)

This report describes research conducted between July 1, 2006 and September 30, 2006 on the use of dry regenerable sorbents for removal of carbon dioxide (CO{sub 2}) from coal combustion flue gas. Modifications to the integrated absorber/ sorbent regenerator/ sorbent cooler system were made to improve sorbent flow consistency and measurement reliability. Operation of the screw conveyor regenerator to achieve a sorbent temperature of at least 120 C at the regenerator outlet is necessary for satisfactory carbon dioxide capture efficiencies in succeeding absorption cycles. Carbon dioxide capture economics in new power plants can be improved by incorporating increased capacity boilers, efficient flue gas desulfurization systems and provisions for withdrawal of sorbent regeneration steam in the design.

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

2006-09-30T23:59:59.000Z

28

Fundamental mechanisms in flue gas conditioning  

SciTech Connect (OSTI)

The overall goal of this research project is to formulate a mathematical model of flue gas conditioning. This model will be based on an understanding of why ask properties, such as cohesivity and resistivity, are changed by conditioning. Such a model could serve as a component of the performance models of particulate control devices where flue gas conditioning is used. There are two specific objectives of this research project, which divide the planned research into two main parts. One part of the project is designed to determine how ash particles are modified by interactions with sorbent injection processes and to describe the mechanisms by which these interactions affect fine particle collection. The objective of the other part of the project is to identify the mechanisms by which conditioning agents, including chemically active compounds, modify the key properties of fine fly ash particles.

Bush, P.V.; Snyder, T.R.

1992-01-09T23:59:59.000Z

29

Alternative formulations of regenerable flue gas cleanup catalysts  

SciTech Connect (OSTI)

The major source of man-made SO{sub 2} in the atmosphere is the burning of coal for electric power generation. Coal-fired utility plants are also large sources of NO{sub x} pollution. Regenerable flue gas desulfurization/NO{sub x} abatement catalysts provide one mechanism of simultaneously removing SO{sub 2} and NO{sub x} species from flue gases released into the atmosphere. The purpose of this project is to examine routes of optimizing the adsorption efficiency, the adsorption capacity, and the ease of regeneration of regenerable flue gas cleanup catalysts. We are investigating two different mechanisms for accomplishing this goal. The first involves the use of different alkali and alkaline earth metals as promoters for the alumina sorbents to increase the surface basicity of the sorbent and thus adjust the number and distribution of adsorption sites. The second involves investigation of non-aqueous impregnation, as opposed to aqueous impregnation, as a method to obtain an evenly dispersed monolayer of the promoter on the surface.

Mitchell, M.B.; White, M.G.

1991-01-01T23:59:59.000Z

30

Re-lining of scrubbers in flue gas desulfurization plants  

SciTech Connect (OSTI)

Rubber lining is used as corrosion protection material in scrubbers, tanks, pipe systems etc of European flue gas desulfurization plants. Although these rubber linings show in cases more than 15 years life, re-rubber lining is still necessary. Due to the expected higher availability of the power station units the time scale of such replacement must be kept to a minimum. As an efficient method for removal of the old lining the high pressure water systems has proven successful. Based on one such case of re-lining the working steps and time scale are demonstrated.

Fenner, J. [Keramchemie GmbH, Siershahn (Germany)

1999-11-01T23:59:59.000Z

31

Relining of scrubbers in flue gas desulfurization plants  

SciTech Connect (OSTI)

Rubber lining is used as a corrosion protection material in European flue gas desulfurization plants, for scrubbers, tanks, pipe systems, etc. Although these rubber linings can last more than 15 years, relining still is necessary. The difficulty of shutting down power station units requires that the time scale of this replacement be kept to a minimum. High-pressure water systems have proven successful as an efficient method for removal of the old lining. The working steps and time scale are demonstrated for one such relining case.

Fenner, J. [Keramchemie GmbH (Germany)

1999-09-01T23:59:59.000Z

32

Catalysts for Oxidation of Mercury in Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Catalysts for Oxidation of Mercury in Flue Gas Catalysts for Oxidation of Mercury in Flue Gas Opportunity The Department of Energy's National Energy Technology Laboratory (NETL) is seeking licensing partners interested in implementing United States Patent Number 7,776,780 entitled "Catalysts for Oxidation of Mercury in Flue Gas." Disclosed in this patent are catalysts for the oxidation of elemental mercury in flue gas. These novel catalysts include iridium (Ir), platinum/iridium (Pt/Ir), and Thief carbons. The catalyst materials will adsorb the oxidizing agents HCl, Cl 2 , and other halogen species in the flue gas stream that are produced when fuel is combusted. These adsorbed oxidizing agents can then react with elemental mercury in the stream, which is difficult to capture, and oxidize it to form Hg (II) species,

33

Novel technologies for SO{sub x}/NO{sub x} removal from flue gas; Technical report, September 1--November 30, 1993  

SciTech Connect (OSTI)

The goal of this research is to develop a low temperature deNO{sub x} catalyst with activity high enough for boiler retrofit applications. Cu-ZrO{sub 2} is a promising low temperature catalyst for the selective reduction of No by propene. At NO = 1000 ppm, propene (C{sub 3}H{sub 6}) = 1000 ppm and 0{sub 2} = 1% and a space velocity of 13,000 h{sup {minus}1}, the NO conversion to N{sub 2} is 64% at 265{degrees}C. The performance of the catalyst, however, does not fulfill the requirement when used for flue gas clean up where the feed is composed of 4% O{sub 2} and 10% H{sub 2}O, and the temperature is 150{degrees}C. Methods to improve the performance of the catalyst are being sought. These include modification of the preparation method such as varying the aging time of the gel after precipitation, and addition of promoters like Pd and Nd to increase the catalytic activity at lower temperatures and higher 0{sub 2} concentrations. Using ethanol (C{sub 2}H{sub 5}OH) instead of C{sub 3}H{sub 6} as a reductant improves the performance of the catalyst when H{sub 2}O is present. Interestingly, methanol is not an effective reductant. Some modified carbon catalysts are also tested. Results on Cu impregnated ASC whetlerite carbon catalyst show 100% N{sub 2} selectivity and 35 % NO conversion at 200{degrees}C. However, the catalyst is unstable and deactivates rapidly. Work planned for the next quarter is to continue to investigate methods to improve the catalytic activity.

Kung, M.; Yang, B. [Northwestern Univ., Chicago, IL (United States); Spivey, J.J.; Agarwal, S.K.; Jang, B.W. [Research Triangle Inst., Durham, NC (United States)

1993-12-31T23:59:59.000Z

34

Separation of Mercury from Flue Gas Desulfurization Scrubber Produced Gypsum  

SciTech Connect (OSTI)

Frontier Geosciences (Frontier; FGS) proposed for DOE Grant No. DE-FG02-07ER84669 that mercury control could be achieved in a wet scrubber by the addition of an amendment to the wet-FGD scrubber. To demonstrate this, a bench-scale scrubber and synthetic flue-gas supply was designed to simulate the limestone fed, wet-desulfurization units utilized by coal-fired power plants. Frontier maintains that the mercury released from these utilities can be controlled and reduced by modifying the existing equipment at installations where wet flue-gas desulfurization (FGD) systems are employed. A key element of the proposal was FGS-PWN, a liquid-based mercury chelating agent, which can be employed as the amendment for removal of all mercury species which enter the wet-FGD scrubber. However, the equipment design presented in the proposal was inadequate to demonstrate these functions and no significant progress was made to substantiate these claims. As a result, funding for a Phase II continuation of this work will not be pursued. The key to implementing the technology as described in the proposal and report appears to be a high liquid-to-gas ratio (L/G) between the flue-gas and the scrubber liquor, a requirement not currently implemented in existing wet-FGD designs. It may be that this constraint can be reduced through parametric studies, but that was not apparent in this work. Unfortunately, the bench-scale system constructed for this project did not function as intended and the funds and time requested were exhausted before the separation studies could occur.

Hensman, Carl, E., P.h.D; Baker, Trevor

2008-06-16T23:59:59.000Z

35

Flue gas desulfurization: Physicochemical and biotechnological approaches  

SciTech Connect (OSTI)

Various flue gas desulfurization processes - physicochemical, biological, and chemobiological - for the reduction of emission of SO{sub 2} with recovery of an economic by-product have been reviewed. The physicochemical processes have been categorized as 'once-through' and 'regenerable.' The prominent once-through technologies include wet and dry scrubbing. The wet scrubbing technologies include wet limestone, lime-inhibited oxidation, limestone forced oxidation, and magnesium-enhanced lime and sodium scrubbing. The dry scrubbing constitutes lime spray drying, furnace sorbent injection, economizer sorbent injection, duct sorbent injection, HYPAS sorbent injection, and circulating fluidized bed treatment process. The regenerable wet and dry processes include the Wellman Lord's process, citrate process, sodium carbonate eutectic process, magnesium oxide process, amine process, aqueous ammonia process, Berglau Forchung's process, and Shell's process. Besides these, the recently developed technologies such as the COBRA process, the OSCAR process, and the emerging biotechnological and chemobiological processes are also discussed. A detailed outline of the chemistry, the advantages and disadvantages, and the future research and development needs for each of these commercially viable processes is also discussed.

Pandey, R.A.; Biswas, R.; Chakrabarti, T.; Devotta, S. [National Environmental Engineering Research Institute, Nagpur (India)

2005-07-01T23:59:59.000Z

36

Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents  

SciTech Connect (OSTI)

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-current downflow reactor system for adsorption of CO{sub 2} and a steam-heated, hollow-screw conveyor system for regeneration of the sorbent and release of a concentrated CO{sub 2} gas stream. An economic analysis of this process (based on the U.S. Department of Energy's National Energy Technology Laboratory's [DOE/NETL's] 'Carbon Capture and Sequestration Systems Analysis Guidelines') was carried out. RTI's economic analyses indicate that installation of the Dry Carbonate Process in a 500 MW{sub e} (nominal) power plant could achieve 90% CO{sub 2} removal with an incremental capital cost of about $69 million and an increase in the cost of electricity (COE) of about 1.95 cents per kWh. This represents an increase of roughly 35.4% in the estimated COE - which compares very favorable versus MEA's COE increase of 58%. Both the incremental capital cost and the incremental COE were projected to be less than the comparable costs for an equally efficient CO{sub 2} removal system based on monoethanolamine (MEA).

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

2007-06-30T23:59:59.000Z

37

Advanced separation technology for flue gas cleanup. Topical report  

SciTech Connect (OSTI)

The objective of this work is to develop a novel system for regenerable SO{sub 2} and NO{sub x} scrubbing of flue gas that focuses on (1) a novel method for regenerating spent SO{sub 2} scrubbing liquor and (2) novel chemistry for reversible absorption of NO{sub x}. In addition, high efficiency hollow fiber contactors (HFC) are proposed as the devices for scrubbing the SO{sub 2} and NO{sub x} from the flue gas. The system will be designed to remove more than 95% of the SO{sub 2} and more than 75% of the NO{sub x} from flue gases typical of pulverized coal-fired power plants at a cost that is at least 20% less than combined wet limestone scrubbing of SO{sub x} and selective catalytic reduction of NO{sub x}. The process will generate only marketable by-products. Our approach is to reduce the capital cost by using high-efficiency hollow fiber devices for absorbing and desorbing the SO{sub 2} and NO{sub x}. We will also introduce new process chemistry to minimize traditionally well-known problems with SO{sub 2} and NO{sub x} absorption and desorption. Our novel chemistry for scrubbing NO{sub x} will consist of water-soluble phthalocyanine compounds invented by SRI as well as polymeric forms of Fe{sup ++} complexes similar to traditional NO{sub x} scrubbing media. The final novelty of our approach is the arrangement of the absorbers in cassette (stackable) form so that the NO{sub x} absorber can be on top of the SO{sub x} absorber. This arrangement is possible only because of the high efficiency of the hollow fiber scrubbing devices, as indicated by our preliminary laboratory data. This arrangement makes it possible for the SO{sub 2} and NO{sub x} scrubbing chambers to be separate without incurring the large ducting and gas pressure drop costs necessary if a second conventional absorber vessel were used. Because we have separate scrubbers, we will have separate liquor loops and simplify the chemical complexity of simultaneous SO{sub 2}/NO{sub x} scrubbing.

Bhown, A.S.; Alvarado, D.; Pakala, N.; Ventura, S. [and others

1995-01-01T23:59:59.000Z

38

Integrated flue gas treatment for simulataneous emission control and heat rate improvement - demonstration project at Ravenswood  

SciTech Connect (OSTI)

Results are presented for electric-utility, residual-oil fired, field demonstration testing of advanced-design, heat-recovery type, flue gas sub-coolers that incorporate sulfite-alkali-based wet scrubbing for efficient removal of volatile and semi-volatile trace elements, sub-micron solid particulate matter, SO{sub 2} and SO{sub 3}. By innovative adaptation of wet collector system operation with methanol injection into the rear boiler cavity to convert flue-gas NO to No{sub 2}, simultaneous removal of NO{sub x} is also achieved. The focus of this integrated flue gas treatment (IFGT) technology development and demonstration-scale, continuous performance testing is an upward-gas-flow, indirectly water-cooled, condensing heat exchanger fitted with acid-proof, teflon-covered tubes and tubesheets and that provides a unique condensing (non-evaporative) wet-scrubbing mode to address air toxics control objectives of new Clean Air Act, Title III. Advantageous trace-metal condensation/nucleation/agglomeration along with substantially enhanced boiler efficiency is accomplished in the IFGT system by use of boiler makeup water as a heat sink in indirectly cooling boiler flue gas to a near-ambient-temperature, low-absolute-humidity, water-saturated state. Moreover, unique, innocuous, stack systems design encountered with conventional high-humidity, wet-scrubber operations. The mechanical design of this advanced flue-gas cooling/scrubbing equipment is based on more than ten years of commercial application of such units is downward-gas-flow design/operation for energy recovery, e.g. in preheating of makeup water, in residual-oil and natural-gas fired boiler operations.

Heaphy, J.; Carbonara, J.; Cressner, A. [Consolidated Edison Company, New York, NY (United States)] [and others

1995-06-01T23:59:59.000Z

39

Construction and testing of a flue-gas corrosion probe  

SciTech Connect (OSTI)

The selection of suitable materials for industrial, waste-heat- recovery systems requires assessment of corrosion of materials in various flue-gas environments. Such assessments involve exposing candidate materials to high-temperature flue gases and analyzing the effects of the exposure conditions. Because corrosion is related to flue-gas chemical composition and temperature, variations in temperature complicate the determination of corrosion rates and corrosion mechanisms. Conversely, a relatively constant temperature allows a more accurate determination of the effects of exposure conditions. For this reason, controlled-temperature flue-gas corrosion probes were constructed and tested for exposure tests of materials. A prototype probe consisted of a silicon carbide tube specimen, supporting hardware, and instrumentation for controlling temperature by internal heating and cooling. An advanced probe included other tubular specimens. Testing of the probes in an industrial-type furnace at a nominal flue-gas temperature of 1200{degree}C revealed that temperature control was inadequate. The cooling mode imposed a substantial axial-temperature gradient on the specimens; while the heating mode imposed a smaller gradient, the heating capacity was very limited. 10 refs., 10 figs., 2 tabs.

Federer, J.I.; McEvers, J.A.

1990-08-01T23:59:59.000Z

40

Oxidation of No to No2 in Flue Gas Plumes of Power Stations  

Science Journals Connector (OSTI)

The oxidation of NO to NO2 in flue gas plumes takes place after release in the ... function of the turbulent mixing rate of flue gas plume and atmospheric air. The effects of ... are illustrated with the measurin...

A. J. Elshout; Dr. S. Beilke

1984-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Evaluation of the Energy Saving Potential from Flue Gas Pressurization  

E-Print Network [OSTI]

details the impact of providing a can be recovered at .1 inch wc. The work of com 500 r----------------------, FLUE GAS TEMPERATURES 200 COUNTER FLOW 100 50 _~,,_ CO-FLOW RECUPERATORS 20 10 SPECIFIC ENERGY, Btu/IbM AIR rl'-h~A:--WORK OF 5... consideration for a convective heat flue gas is entrained, the two are mixed in a exchanger is l600?F for the convective portion of the mixing section, and pressure is then recovered in recuperation equipment. It is significant that for a a diffuser...

Stanton, E. H.

1980-01-01T23:59:59.000Z

42

natural gas+ condensing flue gas heat recovery+ water creation+ CO2  

Open Energy Info (EERE)

natural gas+ condensing flue gas heat recovery+ water creation+ CO2 natural gas+ condensing flue gas heat recovery+ water creation+ CO2 reduction+ cool exhaust gases+ Energy efficiency+ commercial building energy efficiency+ industrial energy efficiency+ power plant energy efficiency+ Home Increase Natural Gas Energy Efficiency Description: Increased natural gas energy efficiency = Reduced utility bills = Profit In 2011 the EIA reports that commercial buildings, industry and the power plants consumed approx. 17.5 Trillion cu.ft. of natural gas. How much of that energy was wasted, blown up chimneys across the country as HOT exhaust into the atmosphere? 40% ~ 60% ? At what temperature? Links: The technology of Condensing Flue Gas Heat Recovery natural gas+ condensing flue gas heat recovery+ water creation+ CO2 reduction+ cool exhaust gases+ Energy efficiency+ commercial building

43

Workshop on sulfur chemistry in flue gas desulfurization  

SciTech Connect (OSTI)

The Flue Gas Desulfurization Workshop was held at Morgantown, West Virginia, June 7-8, 1979. The presentations dealt with the chemistry of sulfur and calcium compounds in scrubbers. DOE and EPRI programs in this area are described. Ten papers have been entered individually into EDB and ERA. (LTN)

Wallace, W.E. Jr.

1980-05-01T23:59:59.000Z

44

Rubber linings as surface protection in flue gas desulfurization plants  

SciTech Connect (OSTI)

The manufacturers of the German rubber lining industry have executed the rubber lining of over 1 million m{sup 2} of steel surfaces in over 150 scrubbers of flue gas desulfurization (FGD) plants, thereby effectively protecting them against corrosion. The application of rubber linings as surface protection in FGD plants has proven effective.

Fenner, J.

1997-04-01T23:59:59.000Z

45

Biomimetic Membrane for CO2 Capture from Flue Gas  

SciTech Connect (OSTI)

These Phase III experiments successfully addressed several issues needed to characterize a permeator system for application to a pulverized coal (PC) burning furnace/boiler assuming typical post-combustion cleanup devices in place. We completed key laboratory stage optimization and modeling efforts needed to move towards larger scale testing. The SOPO addressed six areas. Task 1--Post-Combustion Particle Cleanup--The first object was to determine if the Carbozyme permeator performance was likely to be reduced by particles (materials) in the flue gas stream that would either obstruct the mouth of the hollow fibers (HF) or stick to the HF bore wall surface. The second, based on the Acceptance Standards (see below), was to determine whether it would be preferable to clean the inlet gas stream (removing acid gases and particulates) or to develop methods to clean the Carbozyme permeator if performance declined due to HF block. We concluded that condensation of particle and particulate emissions, in the heat exchanger, could result in the formation of very sticky sulfate aerosols with a strong likelihood of obtruding the HF. These must be managed carefully and minimized to near-zero status before entering the permeator inlet stream. More extensive post-combustion cleanup is expected to be a necessary expense, independent of CO{sub 2} capture technology This finding is in agreement with views now emerging in the literature for a variety of CO{sub 2} capture methods. Task 2--Water Condensation--The key goal was to monitor and control temperature distributions within the permeator and between the permeator and its surroundings to determine whether water condensation in the pores or the HF bore would block flow, decreasing performance. A heat transfer fluid and delivery system were developed and employed. The result was near isothermal performance that avoided all instances of flow block. Direct thermocouple measurements provided the basis for developing a heat transfer model that supports prediction of heat transfer profiles for larger permeators Tasks 3. 4.1, 4.2--Temperature Range of Enzymes--The goal was to determine if the enzyme operating temperature would limit the range of thermal conditions available to the capture system. We demonstrated the ability of various isozymes (enzyme variants) to operate from 4-85 C. Consequently, the operating characteristics of the enzyme are not a controlling factor. Further, any isozyme whose upper temperature bound is at least 10 C greater than that of the planned inlet temperature will be stable under unanticipated, uncontrolled 'hiccups' in power plant operation. Task 4.4, 4.4--Examination of the Effects of SOx and NOx on Enzyme Activity (Development of Flue Gas Composition Acceptance Standards)--The purpose was to define the inlet gas profile boundaries. We examined the potential adverse effects of flue gas constituents including different acids from to develop an acceptance standard and compared these values to actual PC flue gas composition. Potential issues include changes in pH, accumulation of specific inhibitory anions and cations. A model was developed and validated by test with a SO{sub 2}-laden stream. The predicted and actual data very largely coincided. The model predicted feed stream requirements to allow continuous operation in excess of 2500 hours. We developed operational (physical and chemical) strategies to avoid or ameliorate these effects. Avoidance, the preferred strategy (noted above), is accomplished by more extensive cleanup of the flue gas stream. Task 5--Process Engineering Model--We developed a process-engineering model for two purposes. The first was to predict the physical and chemical status at each test point in the design as a basis for scale-up. The second was to model the capital and operating cost of the apparatus. These were accomplished and used to predict capex, opex and cost of energy. Task 6--Preliminary Commercialization Plan--We carried out analyses of the market and the competition by a variety of parameters. The conclusion was that there is a l

Michael C. Trachtenberg

2007-05-31T23:59:59.000Z

46

Direct fired absorption machine flue gas recuperator  

DOE Patents [OSTI]

A recuperator which recovers heat from a gas, generally the combustion gas of a direct-fired generator of an absorption machine. The recuperator includes a housing with liquid flowing therethrough, the liquid being in direct contact with the combustion gas for increasing the effectiveness of the heat transfer between the gas and the liquid.

Reimann, Robert C. (Lafayette, NY); Root, Richard A. (Spokane, WA)

1985-01-01T23:59:59.000Z

47

Effect of V2O5 additive on simultaneous SO2 and NO removal from flue gas over a monolithic cordierite-based CuO/Al2O3 catalyst  

Science Journals Connector (OSTI)

A monolithic cordierite-based CuO/Al2O3 catalyst showed industrial potential for simultaneous SO2 and NO removal from flue gases at 350–400 °C. However, it is still a challenge to prevent CuO from aggregation and to keep it in an active state during the removal and regeneration processes. This work shows that addition of V2O5 to the catalyst can significantly reduce CuO particle size and improve SO2 removal activity, and maintain a high selective catalytic reduction (SCR) activity for NO removal. Furthermore, V2O5 additive prevents aggregation of SiO2 in the cordierite with the coated Al2O3, and inhibits over reduction of the SO2 removal product, CuSO4, during the regeneration by NH3, which are important to the catalyst's stability. V2O5 additive changes the regeneration product from Cu3N to CuO and thus may avoid the temperature rise and \\{NOx\\} release in the subsequent removal process.

Qingya Liu; Zhenyu Liu; Weize Wu

2009-01-01T23:59:59.000Z

48

Near-Zero Emissions Oxy-Combustion Flue Gas Purification  

SciTech Connect (OSTI)

The objectives of this project were to carry out an experimental program to enable development and design of near zero emissions (NZE) CO{sub 2} processing unit (CPU) for oxy-combustion plants burning high and low sulfur coals and to perform commercial viability assessment. The NZE CPU was proposed to produce high purity CO{sub 2} from the oxycombustion flue gas, to achieve > 95% CO{sub 2} capture rate and to achieve near zero atmospheric emissions of criteria pollutants. Two SOx/NOx removal technologies were proposed depending on the SOx levels in the flue gas. The activated carbon process was proposed for power plants burning low sulfur coal and the sulfuric acid process was proposed for power plants burning high sulfur coal. For plants burning high sulfur coal, the sulfuric acid process would convert SOx and NOx in to commercial grade sulfuric and nitric acid by-products, thus reducing operating costs associated with SOx/NOx removal. For plants burning low sulfur coal, investment in separate FGD and SCR equipment for producing high purity CO{sub 2} would not be needed. To achieve high CO{sub 2} capture rates, a hybrid process that combines cold box and VPSA (vacuum pressure swing adsorption) was proposed. In the proposed hybrid process, up to 90% of CO{sub 2} in the cold box vent stream would be recovered by CO{sub 2} VPSA and then it would be recycled and mixed with the flue gas stream upstream of the compressor. The overall recovery from the process will be > 95%. The activated carbon process was able to achieve simultaneous SOx and NOx removal in a single step. The removal efficiencies were >99.9% for SOx and >98% for NOx, thus exceeding the performance targets of >99% and >95%, respectively. The process was also found to be suitable for power plants burning both low and high sulfur coals. Sulfuric acid process did not meet the performance expectations. Although it could achieve high SOx (>99%) and NOx (>90%) removal efficiencies, it could not produce by-product sulfuric and nitric acids that meet the commercial product specifications. The sulfuric acid will have to be disposed of by neutralization, thus lowering the value of the technology to same level as that of the activated carbon process. Therefore, it was decided to discontinue any further efforts on sulfuric acid process. Because of encouraging results on the activated carbon process, it was decided to add a new subtask on testing this process in a dual bed continuous unit. A 40 days long continuous operation test confirmed the excellent SOx/NOx removal efficiencies achieved in the batch operation. This test also indicated the need for further efforts on optimization of adsorption-regeneration cycle to maintain long term activity of activated carbon material at a higher level. The VPSA process was tested in a pilot unit. It achieved CO{sub 2} recovery of > 95% and CO{sub 2} purity of >80% (by vol.) from simulated cold box feed streams. The overall CO{sub 2} recovery from the cold box VPSA hybrid process was projected to be >99% for plants with low air ingress (2%) and >97% for plants with high air ingress (10%). Economic analysis was performed to assess value of the NZE CPU. The advantage of NZE CPU over conventional CPU is only apparent when CO{sub 2} capture and avoided costs are compared. For greenfield plants, cost of avoided CO{sub 2} and cost of captured CO{sub 2} are generally about 11-14% lower using the NZE CPU compared to using a conventional CPU. For older plants with high air intrusion, the cost of avoided CO{sub 2} and capture CO{sub 2} are about 18-24% lower using the NZE CPU. Lower capture costs for NZE CPU are due to lower capital investment in FGD/SCR and higher CO{sub 2} capture efficiency. In summary, as a result of this project, we now have developed one technology option for NZE CPU based on the activated carbon process and coldbox-VPSA hybrid process. This technology is projected to work for both low and high sulfur coal plants. The NZE CPU technology is projected to achieve near zero stack emissions

Minish Shah; Nich Degenstein; Monica Zanfir; Rahul Solunke; Ravi Kumar; Jennifer Bugayong; Ken Burgers

2012-06-30T23:59:59.000Z

49

Industrial Plant for Flue Gas Treatment with High Power Electron Accelerators  

Science Journals Connector (OSTI)

Fossil fuel combustion leads to acidic pollutants like SO2 NOx HCl emission. Different control technologies are proposed however the most popular method is combination of wet FGD (flue gas desulfurization) and SCR (selective catalytic reduction). First using lime or limestone slurry leads to SO2 capture and gypsum is a product. The second process where ammonia is used as reagent and nitrogen oxides are reduced over catalyst surface to gaseous nitrogen removes NOx. New advanced method using electron accelerators for simultaneous SO2 and NOx removal has been developed in Japan the USA Germany and Poland. Both pollutants are removed with high efficiency and byproduct can be applied as fertilizer. Two industrial plants have been already constructed. One in China and second in Poland third one is under construction in Japan. Information on the Polish plant is presented in the paper. Plant has been constructed at Power Station Pomorzany Szczecin (Dolna Odra Electropower Stations Group) and treats flue gases from two Benson boilers 60 MWe and 100 MWth each. Flow rate of the flue gas stream is equal to 270 000 Nm3/h. Four transformer accelerators 700 keV electron energy and 260 kW beam power each were applied. With its 1.05 MW total beam power installed it is a biggest radiation facility over the world nowadays. Description of the plant and results obtained has been presented in the paper.

Andrzej G. Chmielewski; Bogdan Tyminski; Zbigniew Zimek; Andrzej Pawelec; Janusz Licki

2003-01-01T23:59:59.000Z

50

Carbon ion pump for removal of carbon dioxide from combustion gas and other gas mixtures  

DOE Patents [OSTI]

A novel method and system of separating carbon dioxide from flue gas is introduced. Instead of relying on large temperature or pressure changes to remove carbon dioxide from a solvent used to absorb it from flue gas, the ion pump method, as disclosed herein, dramatically increases the concentration of dissolved carbonate ion in solution. This increases the overlying vapor pressure of carbon dioxide gas, permitting carbon dioxide to be removed from the downstream side of the ion pump as a pure gas. The ion pumping may be obtained from reverse osmosis, electrodialysis, thermal desalination methods, or an ion pump system having an oscillating flow in synchronization with an induced electric field.

Aines, Roger D.; Bourcier, William L.

2014-08-19T23:59:59.000Z

51

Carbon ion pump for removal of carbon dioxide from combustion gas and other gas mixtures  

DOE Patents [OSTI]

A novel method and system of separating carbon dioxide from flue gas is introduced. Instead of relying on large temperature or pressure changes to remove carbon dioxide from a solvent used to absorb it from flue gas, the ion pump method, as disclosed herein, dramatically increases the concentration of dissolved carbonate ion in solution. This increases the overlying vapor pressure of carbon dioxide gas, permitting carbon dioxide to be removed from the downstream side of the ion pump as a pure gas. The ion pumping may be obtained from reverse osmosis, electrodialysis, thermal desalination methods, or an ion pump system having an oscillating flow in synchronization with an induced electric field.

Aines, Roger D. (Livermore, CA); Bourcier, William L. (Livermore, CA)

2010-11-09T23:59:59.000Z

52

CO2 Capture Membrane Process for Power Plant Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

CO CO 2 Capture Membrane Process for Power Plant Flue Gas Background The U.S. Department of Energy's (DOE) Existing Plants, Emissions & Capture (EPEC) Program is performing research to develop advanced technologies focusing on carbon dioxide (CO 2 ) emissions control for existing pulverized coal-fired plants. This new focus on post-combustion and oxy-combustion CO 2 emissions control technology, CO 2 compression, and beneficial reuse is in response to the priority for advanced

53

Biominetic Membrane for Co2 Capture from Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Biomimetic Membrane for CO Biomimetic Membrane for CO 2 Capture from Flue Gas Background Carbon Capture and Sequestration (CCS) is a three-step process including capture, pipeline transport, and geologic storage of which the capture of carbon dioxide (CO 2 ) is the most costly and technically challenging. Current available methods impose significant energy burdens that severely impact their overall effectiveness as a significant deployment option. Of the available capture technologies for post

54

E-Print Network 3.0 - advanced flue gas Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

(WTERT) Collection: Renewable Energy 5 INNOVATIVE TECHNOLOGY FOR THE CONTROL OF AIR POLLUTION AT WASTE-TO-ENERGY Summary: -Beam process is applied to flue gas compositions...

55

Analysis of a pilot-scale constructed wetland treatment system for flue gas desulfurization wastewater.  

E-Print Network [OSTI]

??Coal-fired generation accounts for 45% of the United States electricity and generates harmful emissions, such as sulfur dioxide. With the implementation of Flue Gas Desulfurization… (more)

Talley, Mary Katherine

2012-01-01T23:59:59.000Z

56

The Beckett System Recovery and Utilization of Low Grade Waste Heat From Flue Gas  

E-Print Network [OSTI]

. During low demand periods, the unit is gas-fired and produces 150 psi steam at high efficiency. In the fall, the heat exchanger is converted to accept flue gas from the large original water tube boilers. The flue gas heats water, which preheats make...

Henderson, W. R.; DeBiase, J. F.

1983-01-01T23:59:59.000Z

57

Directed evolution of an ultrastable carbonic anhydrase for highly efficient carbon capture from flue gas  

Science Journals Connector (OSTI)

...library generation, and high-throughput...year, coal-fired power plants are...natural-gas–fired power...1. Flue gas from a coal-fired power plant is piped...depleted flue gas is released into...strategy for the generation of very large...

Oscar Alvizo; Luan J. Nguyen; Christopher K. Savile; Jamie A. Bresson; Satish L. Lakhapatri; Earl O. P. Solis; Richard J. Fox; James M. Broering; Michael R. Benoit; Sabrina A. Zimmerman; Scott J. Novick; Jack Liang; James J. Lalonde

2014-01-01T23:59:59.000Z

58

Transport Membrane Condenser for Water and Energy Recovery from Power Plant Flue Gas  

SciTech Connect (OSTI)

The new waste heat and water recovery technology based on a nanoporous ceramic membrane vapor separation mechanism has been developed for power plant flue gas application. The recovered water vapor and its latent heat from the flue gas can increase the power plant boiler efficiency and reduce water consumption. This report describes the development of the Transport Membrane Condenser (TMC) technology in details for power plant flue gas application. The two-stage TMC design can achieve maximum heat and water recovery based on practical power plant flue gas and cooling water stream conditions. And the report includes: Two-stage TMC water and heat recovery system design based on potential host power plant coal fired flue gas conditions; Membrane performance optimization process based on the flue gas conditions, heat sink conditions, and water and heat transport rate requirement; Pilot-Scale Unit design, fabrication and performance validation test results. Laboratory test results showed the TMC system can exact significant amount of vapor and heat from the flue gases. The recovered water has been tested and proved of good quality, and the impact of SO{sub 2} in the flue gas on the membrane has been evaluated. The TMC pilot-scale system has been field tested with a slip stream of flue gas in a power plant to prove its long term real world operation performance. A TMC scale-up design approach has been investigated and an economic analysis of applying the technology has been performed.

Dexin Wang

2012-03-31T23:59:59.000Z

59

Fundamentals of Mercury Oxidation in Flue Gas  

SciTech Connect (OSTI)

The objective of this project is to understand the importance of and the contribution of gas-phase and solid-phase coal constituents in the mercury oxidation reactions. The project involves both experimental and modeling efforts. The team is comprised of the University of Utah, Reaction Engineering International, and the University of Connecticut. The objective is to determine the experimental parameters of importance in the homogeneous and heterogeneous oxidation reactions; validate models; and, improve existing models. Parameters to be studied include HCl, NO{sub x}, and SO{sub 2} concentrations, ash constituents, and temperature. This report summarizes Year 2 results for the experimental and modeling tasks. Experiments in the mercury reactor are underway and interesting results suggested that a more comprehensive look at catalyzed surface reactions was needed. Therefore, much of the work has focused on the heterogeneous reactions. In addition, various chemical kinetic models have been explored in an attempt to explain some discrepancies between this modeling effort and others.

JoAnn S. Lighty; Geoffrey Silcox; Andrew Fry; Constance Senior; Joseph Helble; Balaji Krishnakumar

2005-08-01T23:59:59.000Z

60

ENHANCED CONTROL OF MERCURY BY WET FLUE GAS DESULFURIZATION SYSTEMS  

SciTech Connect (OSTI)

The U.S. Department of Energy and EPRI co-funded this project to improve the control of mercury emissions from coal-fired power plants equipped with wet flue gas desulfurization (FGD) systems. The project has investigated catalytic oxidation of vapor-phase elemental mercury to a form that is more effectively captured in wet FGD systems. If successfully developed, the process could be applicable to over 90,000 MW of utility generating capacity with existing FGD systems, and to future FGD installations. Field tests were conducted to determine whether candidate catalyst materials remain active towards mercury oxidation after extended flue gas exposure. Catalyst life will have a large impact on the cost effectiveness of this potential process. A mobile catalyst test unit was used to test the activity of four different catalyst materials for a period of up to six months each at three utility sites. Catalyst testing was completed at the first site, which fires Texas lignite, in December 1998; at the second test site, which fires a Powder River Basin subbituminous coal, in November 1999; and at the third site, which fires a medium- to high-sulfur bituminous coal, in January 2001. Results of testing at each of the three sites were reported in previous technical notes. At Site 1, catalysts were tested only as powders dispersed in sand bed reactors. At Sites 2 and 3, catalysts were tested in two forms, including powders dispersed in sand and in commercially available forms such as extruded pellets and coated honeycomb structures. This final report summarizes and presents results from all three sites, for the various catalyst forms tested. Field testing was supported by laboratory tests to screen catalysts for activity at specific flue gas compositions, to investigate catalyst deactivation mechanisms and methods for regenerating spent catalysts. Laboratory results are also summarized and discussed in this report.

Unknown

2001-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

Alternative formulations of regenerable flue gas cleanup catalysts. Progress report, September 1, 1990--August 31, 1991  

SciTech Connect (OSTI)

The major source of man-made SO{sub 2} in the atmosphere is the burning of coal for electric power generation. Coal-fired utility plants are also large sources of NO{sub x} pollution. Regenerable flue gas desulfurization/NO{sub x} abatement catalysts provide one mechanism of simultaneously removing SO{sub 2} and NO{sub x} species from flue gases released into the atmosphere. The purpose of this project is to examine routes of optimizing the adsorption efficiency, the adsorption capacity, and the ease of regeneration of regenerable flue gas cleanup catalysts. We are investigating two different mechanisms for accomplishing this goal. The first involves the use of different alkali and alkaline earth metals as promoters for the alumina sorbents to increase the surface basicity of the sorbent and thus adjust the number and distribution of adsorption sites. The second involves investigation of non-aqueous impregnation, as opposed to aqueous impregnation, as a method to obtain an evenly dispersed monolayer of the promoter on the surface.

Mitchell, M.B.; White, M.G.

1991-12-31T23:59:59.000Z

62

Near-zero Emissions Oxy-combustion Flue Gas Purification  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Near-zero Emissions Oxy-combustion Near-zero Emissions Oxy-combustion Flue Gas Purification Background The mission of the U.S. Department of Energy's (DOE) Existing Plants, Emissions & Capture (EPEC) R&D Program is to develop innovative environmental control technologies to enable full use of the nation's vast coal reserves, while allowing the current fleet of coal-fired power plants to comply with existing and emerging environmental regulations. The EPEC R&D Program portfolio of post- and

63

SOx-NOx-Rox Box{trademark} flue gas clean-up demonstration. Final report  

SciTech Connect (OSTI)

Babcock and Wilcox`s (B and W) SOx-NOx-Rox Box{trademark} process effectively removes SOx, NOx and particulate (Rox) from flue gas generated from coal-fired boilers in a single unit operation, a high temperature baghouse. The SNRB technology utilizes dry sorbent injection upstream of the baghouse for removal of SOx and ammonia injection upstream of a zeolitic selective catalytic reduction (SCR) catalyst incorporated in the baghouse to reduce NOx emissions. Because the SOx and NOx removal processes require operation at elevated gas temperatures (800--900 F) for high removal efficiency, high-temperature fabric filter bags are used in the baghouse. The SNRB technology evolved from the bench and laboratory pilot scale to be successfully demonstrated at the 5-MWe field scale. This report represents the completion of Milestone M14 as specified in the Work Plan. B and W tested the SNRB pollution control system at a 5-MWe demonstration facility at Ohio Edison`s R.E. Burger Plant located near Shadyside, Ohio. The design and operation were influenced by the results from laboratory pilot testing at B and W`s Alliance Research Center. The intent was to demonstrate the commercial feasibility of the SNRB process. The SNRB facility treated a 30,000 ACFM flue gas slipstream from Boiler No. 8. Operation of the facility began in May 1992 and was completed in May 1993. About 2,300 hours of high-temperature operation were achieved. The main emissions control performance goals of: greater than 70% SO{sub 2} removal using a calcium-based sorbent; greater than 90% NOx removal with minimal ammonia slip; and particulate emissions in compliance with the New Source Performance Standards (NSPS) of 0.03 lb/million Btu were exceeded simultaneously in the demonstration program when the facility was operated at optimal conditions. Testing also showed significant reductions in emissions of some hazardous air pollutants.

NONE

1995-09-01T23:59:59.000Z

64

Membrane-based carbon capture from flue gas: A review  

Science Journals Connector (OSTI)

Abstract There has been an increasing interest in the application of membranes to flue gas separation, primarily driven by the need of carbon capture for significantly reducing greenhouse gas emissions. Historically, there has not been general consensus about the advantage of membranes against other methods such as liquid solvents for carbon capture. However, recent research indicates that advances in materials and process designs could significantly improve the separation performance of membrane capture systems, which make membrane technology competitive with other technologies for carbon capture. This paper mainly reviews membrane separation for the application to post-combustion CO2 capture with a focus on the developments and breakthroughs in membrane material design, process engineering, and engineering economics.

Rajab Khalilpour; Kathryn Mumford; Haibo Zhai; Ali Abbas; Geoff Stevens; Edward S. Rubin

2014-01-01T23:59:59.000Z

65

Separation of CO2 from flue gas using electrochemical cells  

SciTech Connect (OSTI)

ABSTRACT Past research with high temperature molten carbonate electrochemical cells has shown that carbon dioxide can be separated from flue gas streams produced by pulverized coal combustion for power generation, However, the presence of trace contaminants, i.e" sulfur dioxide and nitric oxides, will impact the electrolyte within the cell. If a lower temperature cell could be devised that would utilize the benefits of commercially-available, upstream desulfurization and denitrification in the power plant, then this CO2 separation technique can approach more viability in the carbon sequestration area, Recent work has led to the assembly and successful operation of a low temperature electrochemical cell. In the proof-of-concept testing with this cell, an anion exchange membrane was sandwiched between gas-diffusion electrodes consisting of nickel-based anode electrocatalysts on carbon paper. When a potential was applied across the cell and a mixture of oxygen and carbon dioxide was flowed over the wetted electrolyte on the cathode side, a stream of CO2 to O2 was produced on the anode side, suggesting that carbonate/ bicarbonate ions are the CO2 carrier in the membrane. Since a mixture of CO 2 and 02 is produced, the possibility exists to use this stream in oxy-firing of additional fuel. From this research, a novel concept for efficiently producing a carbon dioxide rich effiuent from combustion of a fossil fuel was proposed. Carbon dioxide and oxygen are captured from the flue gas of a fossilfuel combustor by one or more electrochemical cells or cell stacks. The separated stream is then transferred to an oxy-fired combustor which uses the gas stream for ancillary combustion, ultimately resulting in an effluent rich in carbon dioxide, A portion of the resulting flow produced by the oxy-fired combustor may be continuously recycled back into the oxy-fired combustor for temperature control and an optimal carbon dioxide rich effluent.

Pennline, H.W; Granite, E.J.; Luebke, D.R; Kitchin, J.R; Landon, J.; Weiland, L.M.

2010-06-01T23:59:59.000Z

66

OpenEI Community - natural gas+ condensing flue gas heat recovery+ water  

Open Energy Info (EERE)

Increase Natural Gas Increase Natural Gas Energy Efficiency http://en.openei.org/community/group/increase-natural-gas-energy-efficiency Description: Increased natural gas energy efficiency = Reduced utility bills = Profit In 2011 the EIA reports that commercial buildings, industry and the power plants consumed approx. 17.5 Trillion cu.ft. of natural gas.How much of that energy was wasted, blown up chimneys across the country as HOT exhaust into the atmosphere? 40% ~ 60% ? At what temperature?gas-energy-efficiency" target="_blank">read more natural gas+ condensing flue gas heat

67

Biomimetric Membrane for CO2 Capture from Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Biomimetic memBrane for co Biomimetic memBrane for co 2 capture from flue Gas Background Carbon Capture and Sequestration (CCS) is a three-step process including capture, pipeline transport and geologic storage of which the capture of carbon dioxide (CO 2 ) is the most costly and technically challenging. Current available methods impose significant energy burdens that severely impact their overall effectiveness as a significant deployment option. Of the available capture technologies for post combustion applications - absorption, adsorption, reaction and membranes chemically facilitated absorption promises to be the most cost-effective membrane solution for post combustion application. The Carbozyme technology extracts CO 2 from low concentration, low pressure sources by means of chemical facilitation of a polymer membrane. The chemical

68

Advanced Flue Gas Desulfurization (AFGD) Demonstration Project, A DOE Assessment  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

8 8 Advanced Flue Gas Desulfurization (AFGD) Demonstration Project A DOE Assessment August 2001 U.S. Department of Energy National Energy Technology Laboratory P.O. Box 880, 3610 Collins Ferry Road Morgantown, WV 26507-0880 and P.O. Box 10940, 626 Cochrans Mill Road Pittsburgh, PA 15236-0940 website: www.netl.doe.gov 2 Disclaimer This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference

69

Membrane Process to Sequester CO2 from Power Plant Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

MeMbrane Process to sequester co MeMbrane Process to sequester co 2 froM Power Plant flue Gas Background Carbon dioxide emissions from coal-fired power plants are believed to contribute significantly to global warming climate change. The direct approach to address this problem is to capture the carbon dioxide in flue gas and sequester it underground. However, the high cost of separating and capturing CO 2 with conventional technologies prevents the adoption of this approach. This project investigates the technical and economic feasibility of a new membrane process to capture CO 2 from power plant flue gas. Description Direct CO 2 capture from power plant flue gas has been the subject of many studies. Currently, CO 2 capture with amine absorption seems to be the leading candidate technology-although membrane processes have been suggested. The principal

70

Flue gas desulfurization : cost and functional analysis of large-scale and proven plants  

E-Print Network [OSTI]

Flue Gas Desulfurization is a method of controlling the emission of sulfurs, which causes the acid rain. The following study is based on 26 utilities which burn coal, have a generating capacity of at least 50 Megawatts ...

Tilly, Jean

1983-01-01T23:59:59.000Z

71

Capture of Carbon Dioxide from Air and Flue Gas in the Alkylamine...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Capture of Carbon Dioxide from Air and Flue Gas in the Alkylamine-Appended Metal-Organic Framework mmen-Mg2(dobpdc) Previous Next List Thomas M. McDonald, Woo Ram Lee, Jarad A....

72

New Developments in Closed Loop Combustion Control Using Flue Gas Analysis  

E-Print Network [OSTI]

New developments in closed loop combustion control are causing radical changes in the way combustion control systems are implemented. The recent availability of in line flue gas analyzers and microprocessor technology are teaming up to produce...

Nelson, R. L.

1981-01-01T23:59:59.000Z

73

Cost-Effective Abatement of Acidifying Emissions with Flue Gas Cleaning Vs. Fuel Switching in Finland  

Science Journals Connector (OSTI)

Acidifying emissions from energy production and industry have decreased considerably during the...e.g. flue gas desulphurization. In this study the Finnish cost curves for SO2 and NOx...were first calculated to p...

N. Karvosenoja; P. Hillukkala; M. Johansson; S. Syril

2001-01-01T23:59:59.000Z

74

CO2 Capture from Flue Gas Using SOlid Molecular Basket Sorbents  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

from Flue Gas Using Solid from Flue Gas Using Solid Molecular Basket Sorbents Background The mission of the U.S. Department of Energy/National Energy Technology Laboratory (DOE/NETL) Existing Plants, Emissions & Capture (EPEC) Research & Development (R&D) Program is to develop innovative environmental control technologies to enable full use of the nation's vast coal reserves, while at the same time allowing the current fleet of coal-

75

Analysis of Halogen-Mercury Reactions in Flue Gas  

SciTech Connect (OSTI)

Oxidized mercury species may be formed in combustion systems through gas-phase reactions between elemental mercury and halogens, such as chorine or bromine. This study examines how bromine species affect mercury oxidation in the gas phase and examines the effects of mixtures of bromine and chlorine on extents of oxidation. Experiments were conducted in a bench-scale, laminar flow, methane-fired (300 W), quartz-lined reactor in which gas composition (HCl, HBr, NO{sub x}, SO{sub 2}) and temperature profile were varied. In the experiments, the post-combustion gases were quenched from flame temperatures to about 350 C, and then speciated mercury was measured using a wet conditioning system and continuous emissions monitor (CEM). Supporting kinetic calculations were performed and compared with measured levels of oxidation. A significant portion of this report is devoted to sample conditioning as part of the mercury analysis system. In combustion systems with significant amounts of Br{sub 2} in the flue gas, the impinger solutions used to speciate mercury may be biased and care must be taken in interpreting mercury oxidation results. The stannous chloride solution used in the CEM conditioning system to convert all mercury to total mercury did not provide complete conversion of oxidized mercury to elemental, when bromine was added to the combustion system, resulting in a low bias for the total mercury measurement. The use of a hydroxylamine hydrochloride and sodium hydroxide solution instead of stannous chloride showed a significant improvement in the measurement of total mercury. Bromine was shown to be much more effective in the post-flame, homogeneous oxidation of mercury than chlorine, on an equivalent molar basis. Addition of NO to the flame (up to 400 ppmv) had no impact on mercury oxidation by chlorine or bromine. Addition of SO{sub 2} had no effect on mercury oxidation by chlorine at SO{sub 2} concentrations below about 400 ppmv; some increase in mercury oxidation was observed at SO{sub 2} concentrations of 400 ppmv and higher. In contrast, SO{sub 2} concentrations as low as 50 ppmv significantly reduced mercury oxidation by bromine, this reduction could be due to both gas and liquid phase interactions between SO{sub 2} and oxidized mercury species. The simultaneous presence of chlorine and bromine in the flue gas resulted in a slight increase in mercury oxidation above that obtained with bromine alone, the extent of the observed increase is proportional to the chlorine concentration. The results of this study can be used to understand the relative importance of gas-phase mercury oxidation by bromine and chlorine in combustion systems. Two temperature profiles were tested: a low quench (210 K/s) and a high quench (440 K/s). For chlorine the effects of quench rate were slight and hard to characterize with confidence. Oxidation with bromine proved sensitive to quench rate with significantly more oxidation at the lower rate. The data generated in this program are the first homogeneous laboratory-scale data on bromine-induced oxidation of mercury in a combustion system. Five Hg-Cl and three Hg-Br mechanisms, some published and others under development, were evaluated and compared to the new data. The Hg-halogen mechanisms were combined with submechanisms from Reaction Engineering International for NO{sub x}, SO{sub x}, and hydrocarbons. The homogeneous kinetics under-predicted the levels of mercury oxidation observed in full-scale systems. This shortcoming can be corrected by including heterogeneous kinetics in the model calculations.

Paula Buitrago; Geoffrey Silcox; Constance Senior; Brydger Van Otten

2010-01-01T23:59:59.000Z

76

Current status of MHI CO2 capture plant technology, large scale demonstration project and road map to commercialization for coal fired flue gas application  

Science Journals Connector (OSTI)

(1) It is becoming increasingly evident that the prolonged utilization of fossil fuels for primary energy production, especially coal which is relatively cheap and abundant, is inevitable and that Carbon Capture and Storage (CCS) technology can significantly reduce CO2 emissions from this sector thus allowing the continued environmentally sustainable use of this important energy commodity on a global basis. (2) MHI has co-developed the Kansai Mitsubishi Carbon Dioxide Recovery Process (KM-CDR Process™) and KS-1™ absorbent, which has been deployed in seven CO2 capture plants, now under commercial operation operating at a CO2 capture capacity of 450 metric tons per day (tpd). In addition, a further two commercial plants are now under construction all of which capture CO2 from natural gas fired flue gas boilers and steam reformers. Accordingly this technology is now available for commercial scale CO2 capture for gas boiler and gas turbine application. (3) However before offering commercial CO2 capture plants for coal fired flue gas application, it is necessary to verify the influence of, and develop countermeasures for, related impurities contained in coal fired flue gas. This includes the influence on both the absorbent and the entire system of the CO2 capture plant to achieve high operational reliability and minimize maintenance requirements. (4) Preventing the accumulation of impurities, especially the build up of dust, is very important when treating coal fired flue gas and MHI has undertaken significant work to understand the impact of impurities in order to achieve reliable and stable operating conditions and to efficiently optimize integration between the CO2 capture plant, the coal fired power plant and the flue gas clean up equipment. (5) To achieve this purpose, MHI constructed a 10 tpd CO2 capture demonstration plant at the Matsushima 1000 MW Power Station and confirmed successful, long term demonstration following ?5000 hours of operation in 2006–07 with 50% financial support by RITE, as a joint program to promote technological development with the private sector, and cooperation from J-POWER. (6) Following successful demonstration testing at Matsushima, additional testing was undertaken in 2008 to examine the impact of entrainment of higher levels of flue gas impurities (primarily \\{SOx\\} and dust by bypassing the existing FGD) and to determine which components of the CO2 recovery process are responsible for the removal of these impurities. Following an additional 1000 demonstration hours, results indicated stable operational performance in relation to the following impurities; (1) SO2: Even at higher SO2 concentrations were almost completely removed from the flue gas before entering the CO2 absorber. (2) Dust: The accumulation of dust in the absorbent was higher, leading to an advanced understanding of the behavior of dust in the CO2 capture plant and the dust removal efficiency of each component within the CO2 recovery system. The data obtained is useful for the design of large-scale units and confirms the operating robustness of the CO2 capture plant accounting for wide fluctuations in impurity concentrations. (7) This important coal fired flue gas testing showed categorically that minimizing the accumulation of large concentrations of impurities, and to suppress dust concentrations below a prescribed level, is important to achieve long-term stable operation and to minimize maintenance work for the CO2 capture plant. To comply with the above requirement, various countermeasures have been developed which include the optimization of the impurity removal technology, flue gas pre treatment and improved optimization with the flue gas desulfurization facility. (8) In case of a commercial scale CO2 capture plant applied for coal fired flue gas, its respective size will be several thousand tpd which represents a considerable scale-up from the 10 tpd demonstration plant. In order to ensure the operational reliability and to accurately confirm the influence and the behavior of the impurities in coal fired fl

Takahiko Endo; Yoshinori Kajiya; Hiromitsu Nagayasu; Masaki Iijima; Tsuyoshi Ohishi; Hiroshi Tanaka; Ronald Mitchell

2011-01-01T23:59:59.000Z

77

JV Task 124 - Understanding Multi-Interactions of SO3, Mercury, Selenium, and Arsenic in Illinois Coal Flue Gas  

SciTech Connect (OSTI)

This project consisted of pilot-scale combustion testing with a representative Illinois basin coal to explore the multi-interactions of SO{sub 3}, mercury, selenium and arsenic. The parameters investigated for SO{sub 3} and mercury interactions included different flue gas conditions, i.e., temperature, moisture content, and particulate alkali content, both with and without activated carbon injection for mercury control. Measurements were also made to track the transformation of selenium and arsenic partitioning as a function of flue gas temperature through the system. The results from the mercury-SO{sub 3} testing support the concept that SO{sub 3} vapor is the predominant factor that impedes efficient mercury removal with activated carbon in an Illinois coal flue gas, while H{sub 2}SO{sub 4} aerosol has less impact on activated carbon injection performance. Injection of a suitably mobile and reactive additives such as sodium- or calcium-based sorbents was the most effective strategy tested to mitigate the effect of SO{sub 3}. Transformation measurements indicate a significant fraction of selenium was associated with the vapor phase at the electrostatic precipitator inlet temperature. Arsenic was primarily particulate-bound and should be captured effectively with existing particulate control technology.

Ye Zhuang; Christopher Martin; John Pavlish

2009-03-31T23:59:59.000Z

78

PRODUCTION OF CONSTRUCTION AGGREGATES FROM FLUE GAS DESULFURIZATION SLUDGE  

SciTech Connect (OSTI)

Through a cooperative agreement with DOE, the Research and Development Department of CONSOL Inc. (CONSOL R and D) is teaming with SynAggs, Inc. and Duquesne Light to design, construct, and operate a 500 lb/h continuous pilot plant to produce road construction aggregate from a mixture of wet flue gas desulfurization (FGD) sludge, fly ash, and other components. The proposed project is divided into six tasks: (1) Project Management; (2) Mix Design Evaluation; (3) Process Design; (4) Construction; (5) Start-Up and Operation; and (6) Reporting. In this quarter, Tasks 1 and 2 were completed. A project management plan (Task 1) was issued to DOE on October 22, 1998 . The mix design evaluation (Task 2) with Duquesne Light Elrama Station FGD sludge and Allegheny Power Hatfields Ferry Station fly ash was completed. Eight semi-continuous bench-scale tests were conducted to examine the effects of mix formulation on aggregate properties. A suitable mix formulation was identified to produce aggregates that meet specifications of the American Association of State High Transport Officials (AASHTO) as Class A aggregate for use in highway construction. The mix formulation was used in designing the flow sheet of the pilot plant. The process design (Task 3) is approximately 80% completed. Equipment was evaluated to comply with design requirements. The design for the curing vessel was completed by an outside engineering firm. All major equipment items for the pilot plant, except the curing vessel, were ordered. Pilot plant construction (Task 4) was begun in October. The Hazardous Substance Plan was issued to DOE. The Allegheny County (PA) Heat Department determined that an air emission permit is not required for operation of the pilot plant.

NONE

1998-12-01T23:59:59.000Z

79

Partitioning of mercury, arsenic, selenium, boron, and chloride in a full-scale coal combustion process equipped with selective catalytic reduction, electrostatic precipitation, and flue gas desulfurization systems  

SciTech Connect (OSTI)

A full-scale field study was carried out at a 795 MWe coal-fired power plant equipped with selective catalytic reduction (SCR), an electrostatic precipitator (ESP), and wet flue gas desulfurization (FGD) systems to investigate the distribution of selected trace elements (i.e., mercury, arsenic, selenium, boron, and chloride) from coal, FGD reagent slurry, makeup water to flue gas, solid byproduct, and wastewater streams. Flue gases were collected from the SCR outlet, ESP inlet, FGD inlet, and stack. Concurrent with flue gas sampling, coal, bottom ash, economizer ash, and samples from the FGD process were also collected for elemental analysis. By combining plant operation parameters, the overall material balances of selected elements were established. The removal efficiencies of As, Se, Hg, and B by the ESP unit were 88, 56, 17, and 8%, respectively. Only about 2.5% of Cl was condensed and removed from flue gas by fly ash. The FGD process removed over 90% of Cl, 77% of B, 76% of Hg, 30% of Se, and 5% of As. About 90% and 99% of the FGD-removed Hg and Se were associated with gypsum. For B and Cl, over 99% were discharged from the coal combustion process with the wastewater. Mineral trona (trisodium hydrogendicarbonate dehydrate, Na{sub 3}H(CO{sub 3}){sub 2}.2H{sub 2}O) was injected before the ESP unit to control the emission of sulfur trioxide (SO{sub 3}). By comparing the trace elements compositions in the fly ash samples collected from the locations before and after the trona injection, the injection of trona did not show an observable effect on the partitioning behaviors of selenium and arsenic, but it significantly increased the adsorption of mercury onto fly ash. The stack emissions of mercury, boron, selenium, and chloride were for the most part in the gas phase. 47 refs., 3 figs., 11 tabs.

Chin-Min Cheng; Pauline Hack; Paul Chu; Yung-Nan Chang; Ting-Yu Lin; Chih-Sheng Ko; Po-Han Chiang; Cheng-Chun He; Yuan-Min Lai; Wei-Ping Pan [Western Kentucky University, Bowling Green, KY (United States). Institute for Combustion Science and Environmental Technology

2009-09-15T23:59:59.000Z

80

Zero Liquid Discharge (ZLD) System for Flue-Gas Derived Water From Oxy-Combustion Process  

SciTech Connect (OSTI)

Researchers at the National Energy Technology Laboratory (NETL) located in Albany, Oregon, have patented a process - Integrated Pollutant Removal (IPR) that uses off-the-shelf technology to produce a sequestration ready CO{sub 2} stream from an oxy-combustion power plant. Capturing CO{sub 2} from fossil-fuel combustion generates a significant water product which can be tapped for use in the power plant and its peripherals. Water condensed in the IPR{reg_sign} process may contain fly ash particles, sodium (from pH control), and sulfur species, as well as heavy metals, cations and anions. NETL is developing a treatment approach for zero liquid discharge while maximizing available heat from IPR. Current treatment-process steps being studied are flocculation/coagulation, for removal of cations and fine particles, and reverse osmosis, for anion removal as well as for scavenging the remaining cations. After reverse osmosis process steps, thermal evaporation and crystallization steps will be carried out in order to build the whole zero liquid discharge (ZLD) system for flue-gas condensed wastewater. Gypsum is the major product from crystallization process. Fast, in-line treatment of water for re-use in IPR seems to be one practical step for minimizing water treatment requirements for CO{sub 2} capture. The results obtained from above experiments are being used to build water treatment models.

Sivaram Harendra; Danylo Oryshchyn; Thomas Ochs; Stephen J. Gerdemann; John Clark

2011-10-16T23:59:59.000Z

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81

SOx-NOx-Rox Box{trademark} flue gas clean-up demonstration. Final report  

SciTech Connect (OSTI)

The SNRB{trademark} Flue Gas Cleanup Demonstration Project was cooperatively funded by the U.S. Department of Energy (DOE), the Ohio Coal Development Office (OCDO), B&W, the Electric Power Research Institute (EPRI), Ohio Edison, Norton Chemical Process Products Company and the 3M Company. The SNRB{trademark} technology evolved from the bench and laboratory pilot scale to be successfully demonstrated at the 5-MWe field scale. Development of the SNRB{trademark} process at B&W began with pilot testing of high-temperature dry sorbent injection for SO{sub 2} removal in the 1960`s. Integration of NO{sub x} reduction was evaluated in the 1970`s. Pilot work in the 1980`s focused on evaluation of various NO{sub x} reduction catalysts, SO{sub 2} sorbents and integration of the catalyst with the baghouse. This early development work led to the issuance of two US process patents to B&W - No. 4,309,386 and No. 4,793,981. An additional patent application for improvements to the process is pending. The OCDO was instrumental in working with B&W to develop the process to the point where a larger scale demonstration of the technology was feasible. This report represents the completion of Milestone M14 as specified in the Work Plan. B&W tested the SNRB{trademark} pollution control system at a 5-MWe demonstration facility at Ohio Edison`s R. E. Burger Plant located near Shadyside, Ohio. The design and operation were influenced by the results from laboratory pilot testing at B&W`s Alliance Research Center. The intent was to demonstrate the commercial feasibility of the SNRB{trademark} process. The SNRB{trademark} facility treated a 30,000 ACFM flue gas slipstream from Boiler No. 8. Operation of the facility began in May 1992 and was completed in May 1993.

NONE

1995-09-01T23:59:59.000Z

82

Permitting and solid waste management issues for the Bailly Station wet limestone Advanced Flue Gas Desulfurization (AFGD) system  

SciTech Connect (OSTI)

Pure Air (a general partnership between Air Products and Chemicals, Inc., and Mitsubishi Heavy Industries America, Inc.). is constructing a wet limestone co-current advanced flue gas desulfurization (AFGD) system that has technological and commercial advantages over conventional FGD systems in the United States. The AFGD system is being installed at the Northern Indiana Public Service Company's Bailly Generating Station near Gary, Indiana. The AFGD system is scheduled to be operational by the Summer, 1992. The AFGD system will remove at least 90 percent of the sulfur dioxide (SO{sub 2}) in the flue gas from Boilers 7 and 8 at the Station while burning 3.2 percent sulfur coal. Also as part of testing the AFGD system, 95 percent removal of SO{sub 2} will be demonstrated on coals containing up to 4.5 percent sulfur. At the same time that SO{sub 2} is removed from the flue gas, a gypsum by-product will be produced which will be used for wallboard manufacturing. Since the AFGD system is a pollution control device, one would expect its installation to be received favorably by the public and regulatory agencies. Although the project was well received by regulatory agencies, on public group (Save the Dunes Council) was initially concerned since the project is located adjacent to the Indiana Dunes National Lakeshore. The purpose of this paper is to describe the project team's experiences in obtaining permits/approvals from regulatory agencies and in dealing with the public. 1 ref., 1 fig., 2 tabs.

Bolinsky, F.T. (Pure Air, Allentown, PA (United States)); Ross, J. (Northern Indiana Public Service Co., Hammond, IN (United States)); Dennis, D.S. (United Engineers and Constructors, Inc., Denver, CO (United States). Stearns-Roger Div.); Huston, J.S. (Environmental Alternatives, Inc., Warren NJ (USA))

1991-01-01T23:59:59.000Z

83

Dynamic Tests and Results in an Oxy-fuel Circulating Fluidized Bed Combustor with Warm Flue Gas Recycle  

Science Journals Connector (OSTI)

Dynamic Tests and Results in an Oxy-fuel Circulating Fluidized Bed Combustor with Warm Flue Gas Recycle ... Dynamic step change tests concerning the coal feed rate and coal type were conducted. ... In the dynamic tests, the oxygen concentration in the flue gas fluctuates in the form of a sinusoidal wave because of the fast volatile combustion and the delay in the char ignition. ...

Jian-xin Zhou; Zhuang Shao; Feng-qi Si; Zhi-gao Xu

2014-11-17T23:59:59.000Z

84

Effect of connate water on miscible displacement of reservoir oil by flue gas  

E-Print Network [OSTI]

Average Reservoir Fluid Pro erties Before Break- Through Ultimate Economic Re cover Fraction OIP 1(a) (b) (c) 2(a) (b) (c) 3(a) (b) (c) (b) (c) (d) 5(*) (b) (c} 6(a) (b) (c) 3800 4200 4600 3800 4200 4600 3800 4ZOO 4600 3000...-through recovery of 75 per cent. Nitrogen resulted in an 81 per cent break- through recovery, after reaching miscibility at 4160 psi. Although nitrogen gave a higher break-through recovery than flue gas, flue gas 25 0. 80 4600 psi 4200 psi f4 0 0 0 'g 4...

Maxwell, H. D.

2012-06-07T23:59:59.000Z

85

Near-Zero Emissions Oxy-Combustion Flue Gas Purification - Power Plant Performance  

SciTech Connect (OSTI)

A technical feasibility assessment was performed for retrofitting oxy-fuel technology to an existing power plant burning low sulfur PRB fuel and high sulfur bituminous fuel. The focus of this study was on the boiler/power generation island of a subcritical steam cycle power plant. The power plant performance in air and oxy-firing modes was estimated and modifications required for oxy-firing capabilities were identified. A 460 MWe (gross) reference subcritical PC power plant was modeled. The reference air-fired plant has a boiler efficiency (PRB/Bituminous) of 86.7%/89.3% and a plant net efficiency of 35.8/36.7%. Net efficiency for oxy-fuel firing including ASU/CPU duty is 25.6%/26.6% (PRB/Bituminous). The oxy-fuel flue gas recirculation flow to the boiler is 68%/72% (PRB/bituminous) of the flue gas (average O{sub 2} in feed gas is 27.4%/26.4%v (PRB/bituminous)). Maximum increase in tube wall temperature is less than 10ºF for oxy-fuel firing. For oxy-fuel firing, ammonia injected to the SCR was shut-off and the FGD is applied to remove SOx from the recycled primary gas stream and a portion of the SOx from the secondary stream for the high sulfur bituminous coal. Based on CFD simulations it was determined that at the furnace outlet compared to air-firing, SO{sub 3}/SO{sub 2} mole ratio is about the same, NOx ppmv level is about the same for PRB-firing and 2.5 times for bituminous-firing due to shutting off the OFA, and CO mole fraction is approximately double. A conceptual level cost estimate was performed for the incremental equipment and installation cost of the oxyfuel retrofit in the boiler island and steam system. The cost of the retrofit is estimated to be approximately 81 M$ for PRB low sulfur fuel and 84 M$ for bituminous high sulfur fuel.

Andrew Seltzer; Zhen Fan

2011-03-01T23:59:59.000Z

86

Carbon dioxide absorber and regeneration assemblies useful for power plant flue gas  

DOE Patents [OSTI]

Disclosed are apparatus and method to treat large amounts of flue gas from a pulverized coal combustion power plant. The flue gas is contacted with solid sorbents to selectively absorb CO.sub.2, which is then released as a nearly pure CO.sub.2 gas stream upon regeneration at higher temperature. The method is capable of handling the necessary sorbent circulation rates of tens of millions of lbs/hr to separate CO.sub.2 from a power plant's flue gas stream. Because pressurizing large amounts of flue gas is cost prohibitive, the method of this invention minimizes the overall pressure drop in the absorption section to less than 25 inches of water column. The internal circulation of sorbent within the absorber assembly in the proposed method not only minimizes temperature increases in the absorber to less than 25.degree. F., but also increases the CO.sub.2 concentration in the sorbent to near saturation levels. Saturating the sorbent with CO.sub.2 in the absorber section minimizes the heat energy needed for sorbent regeneration. The commercial embodiments of the proposed method can be optimized for sorbents with slower or faster absorption kinetics, low or high heat release rates, low or high saturation capacities and slower or faster regeneration kinetics.

Vimalchand, Pannalal; Liu, Guohai; Peng, Wan Wang

2012-11-06T23:59:59.000Z

87

Flue gas carbon dioxide sequestration during water softening with ion-exchange fibers  

SciTech Connect (OSTI)

This study examines the use of ion-exchange fibers (IX fibers) to permanently sequester carbon dioxide present in flue gas into an aqueous phase as calcium or magnesium alkalinity while concurrently softening hard water. The only process inputs besides carbon dioxide (or flue gas) are snowmelt (or rainwater); no other chemicals are required for the regeneration of the IX fibers. Importantly, the process is not energy intensive and carbon dioxide does not need to be compressed to excessive pressures (>150 psi) for efficient use. Sources of carbon dioxide do not require concentration and, therefore, the use of raw flue gas (similar to 17% CO{sub 2}) is feasible with the rate of sequestration governed only by the partial pressure of carbon dioxide. While valid for flue gas obtained from any combustion process (e.g., coal, oil, natural gas, etc.), emissions from oil or gas combustion may be more appropriate for use in the described process due to the absence of mercury and particulates. It should also be noted that the presence of sulfur dioxide in flue gas would not adversely affect the process and may even enhance regeneration efficiency. The only product of the proposed process is an environmentally benign regenerant stream containing calcium and/or magnesium alkalinity. The unique property of IX fibers that makes the proposed process both environmentally sustainable and economically feasible is amenability to efficient regeneration with carbon dioxide and harvested snowmelt. Low intraparticle diffusional resistance is the underlying reason why IX fibers are amenable to efficient regeneration using snowmelt sparged with carbon dioxide; 95% calcium recovery was attained at a CO{sub 2} partial pressure of 6.8 atm. The energy balance for a typical electric utility shows that up to 1% of carbon dioxide emitted during combustion would be sequestered in the softening process.

Greenleaf, J.E.; SenGupta, A.K. [Lafayette College, Easton, PA (United States). Dept. of Civil & Environmental Engineering

2009-06-15T23:59:59.000Z

88

Nitrogen removal from natural gas  

SciTech Connect (OSTI)

According to a 1991 Energy Information Administration estimate, U.S. reserves of natural gas are about 165 trillion cubic feet (TCF). To meet the long-term demand for natural gas, new gas fields from these reserves will have to be developed. Gas Research Institute studies reveal that 14% (or about 19 TCF) of known reserves in the United States are subquality due to high nitrogen content. Nitrogen-contaminated natural gas has a low Btu value and must be upgraded by removing the nitrogen. In response to the problem, the Department of Energy is seeking innovative, efficient nitrogen-removal methods. Membrane processes have been considered for natural gas denitrogenation. The challenge, not yet overcome, is to develop membranes with the required nitrogen/methane separation characteristics. Our calculations show that a methane-permeable membrane with a methane/nitrogen selectivity of 4 to 6 would make denitrogenation by a membrane process viable. The objective of Phase I of this project was to show that membranes with this target selectivity can be developed, and that the economics of the process based on these membranes would be competitive. Gas permeation measurements with membranes prepared from two rubbery polymers and a superglassy polymer showed that two of these materials had the target selectivity of 4 to 6 when operated at temperatures below - 20{degrees}C. An economic analysis showed that a process based on these membranes is competitive with other technologies for small streams containing less than 10% nitrogen. Hybrid designs combining membranes with other technologies are suitable for high-flow, higher-nitrogen-content streams.

NONE

1997-04-01T23:59:59.000Z

89

Transport Membrane Condenser for Water and Energy Recovery from Power Plant Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Dexin Wang Dexin Wang Principal Investigator Gas Technology Institute 1700 South Mount Prospect Rd Des Plaines, Il 60018 847-768-0533 dexin.wang@gastechnology.org TransporT MeMbrane Condenser for WaTer and energy reCovery froM poWer planT flue gas proMIs/projeCT no.: nT0005350 Background One area of the U.S. Department of Energy's (DOE) Innovations for Existing Plants (IEP) Program's research is being performed to develop advanced technologies to reuse power plant cooling water and associated waste heat and to investigate methods to recover water from power plant flue gas. Considering the quantity of water withdrawn and consumed by power plants, any recovery or reuse of this water can significantly reduce the plant's water requirements. Coal occurs naturally with water present (3-60 weight %), and the combustion

90

MEMBRANE PROCESS TO SEQUESTER CO2 FROM POWER PLANT FLUE GAS  

SciTech Connect (OSTI)

The objective of this project was to assess the feasibility of using a membrane process to capture CO2 from coal-fired power plant flue gas. During this program, MTR developed a novel membrane (Polaris™) with a CO2 permeance tenfold higher than commercial CO2-selective membranes used in natural gas treatment. The Polaris™ membrane, combined with a process design that uses a portion of combustion air as a sweep stream to generate driving force for CO2 permeation, meets DOE post-combustion CO2 capture targets. Initial studies indicate a CO2 separation and liquefaction cost of $20 - $30/ton CO2 using about 15% of the plant energy at 90% CO2 capture from a coal-fired power plant. Production of the Polaris™ CO2 capture membrane was scaled up with MTR’s commercial casting and coating equipment. Parametric tests of cross-flow and countercurrent/sweep modules prepared from this membrane confirm their near-ideal performance under expected flue gas operating conditions. Commercial-scale, 8-inch diameter modules also show stable performance in field tests treating raw natural gas. These findings suggest that membranes are a viable option for flue gas CO2 capture. The next step will be to conduct a field demonstration treating a realworld power plant flue gas stream. The first such MTR field test will capture 1 ton CO2/day at Arizona Public Service’s Cholla coal-fired power plant, as part of a new DOE NETL funded program.

Tim Merkel; Karl Amo; Richard Baker; Ramin Daniels; Bilgen Friat; Zhenjie He; Haiqing Lin; Adrian Serbanescu

2009-03-31T23:59:59.000Z

91

Recovery of Water from Boiler Flue Gas Using Condensing Heat Exchangers  

SciTech Connect (OSTI)

Most of the water used in a thermoelectric power plant is used for cooling, and DOE has been focusing on possible techniques to reduce the amount of fresh water needed for cooling. DOE has also been placing emphasis on recovery of usable water from sources not generally considered, such as mine water, water produced from oil and gas extraction, and water contained in boiler flue gas. This report deals with development of condensing heat exchanger technology for recovering moisture from flue gas from coal-fired power plants. The report describes: (1) An expanded data base on water and acid condensation characteristics of condensing heat exchangers in coal-fired units. This data base was generated by performing slip stream tests at a power plant with high sulfur bituminous coal and a wet FGD scrubber and at a power plant firing high-moisture, low rank coals. (2) Data on typical concentrations of HCl, HNO{sub 3} and H{sub 2}SO{sub 4} in low temperature condensed flue gas moisture, and mercury capture efficiencies as functions of process conditions in power plant field tests. (3) Theoretical predictions for sulfuric acid concentrations on tube surfaces at temperatures above the water vapor dewpoint temperature and below the sulfuric acid dew point temperature. (4) Data on corrosion rates of candidate heat exchanger tube materials for the different regions of the heat exchanger system as functions of acid concentration and temperature. (5) Data on effectiveness of acid traps in reducing sulfuric acid concentrations in a heat exchanger tube bundle. (6) Condensed flue gas water treatment needs and costs. (7) Condensing heat exchanger designs and installed capital costs for full-scale applications, both for installation immediately downstream of an ESP or baghouse and for installation downstream of a wet SO{sub 2} scrubber. (8) Results of cost-benefit studies of condensing heat exchangers.

Edward Levy; Harun Bilirgen; John DuPoint

2011-03-31T23:59:59.000Z

92

Recovery of Water from Boiler Flue Gas Using Condensing Heat Exchangers  

SciTech Connect (OSTI)

Most of the water used in a thermoelectric power plant is used for cooling, and DOE has been focusing on possible techniques to reduce the amount of fresh water needed for cooling. DOE has also been placing emphasis on recovery of usable water from sources not generally considered, such as mine water, water produced from oil and gas extraction, and water contained in boiler flue gas. This report deals with development of condensing heat exchanger technology for recovering moisture from flue gas from coal-fired power plants. The report describes: • An expanded data base on water and acid condensation characteristics of condensing heat exchangers in coal-fired units. This data base was generated by performing slip stream tests at a power plant with high sulfur bituminous coal and a wet FGD scrubber and at a power plant firing highmoisture, low rank coals. • Data on typical concentrations of HCl, HNO{sub 3} and H{sub 2}SO{sub 4} in low temperature condensed flue gas moisture, and mercury capture efficiencies as functions of process conditions in power plant field tests. • Theoretical predictions for sulfuric acid concentrations on tube surfaces at temperatures above the water vapor dewpoint temperature and below the sulfuric acid dew point temperature. • Data on corrosion rates of candidate heat exchanger tube materials for the different regions of the heat exchanger system as functions of acid concentration and temperature. • Data on effectiveness of acid traps in reducing sulfuric acid concentrations in a heat exchanger tube bundle. • Condensed flue gas water treatment needs and costs. • Condensing heat exchanger designs and installed capital costs for full-scale applications, both for installation immediately downstream of an ESP or baghouse and for installation downstream of a wet SO{sub 2} scrubber. • Results of cost-benefit studies of condensing heat exchangers.

Levy, Edward; Bilirgen, Harun; DuPont, John

2011-03-31T23:59:59.000Z

93

Life cycle considerations of the flue gas desulphurization system at a lignite-fired power plant in Thailand  

Science Journals Connector (OSTI)

The Flue Gas Desulphurization (FGD) system has been installed at the biggest lignite-fired power generation plant in Thailand to reduce the large...2...emission. In order to understand the costs and benefits, bot...

Sate Sampattagul; Seizo Kato…

2004-11-01T23:59:59.000Z

94

Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas  

SciTech Connect (OSTI)

The objective of this project is to demonstrate an innovative process to mineralize CO2 from flue gas directly to reactive carbonates and maximize the value and versatility of its beneficial use products. The program scope includes the design, construction, and testing of a CO2 Conversion to Material Products (CCMP) Pilot Demonstration Plant utilizing CO2 from the flue gas of a power production facility in Moss Landing, CA as well as flue gas from coal combustion. This topical report covers Phase 2b, which is the construction phase of pilot demonstration subsystems that make up the integrated plant. The subsystems included are the mineralization subsystem, the Alkalinity Based on Low Energy (ABLE) subsystem, the waste calcium oxide processing subsystem, and the fiber cement board production subsystem. The fully integrated plant is now capable of capturing CO2 from various sources (gas and coal) and mineralizing into a reactive calcium carbonate binder and subsequently producing commercial size (4ftx8ft) fiber cement boards. The topical report provides a description of the “as built” design of these subsystems and the results of the commissioning activities that have taken place to confirm operability. At the end of Phase 2b, the CCMP pilot demonstration is fully ready for testing.

Devenney, Martin; Gilliam, Ryan; Seeker, Randy

2014-06-01T23:59:59.000Z

95

Flue Gas Purification Utilizing SOx/NOx Reactions During Compressin of CO2 Derived from Oxyfuel Combustion  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Flue Gas Purification Flue Gas Purification Utilizing SO X /NO X Reactions During Compression of CO 2 Derived from Oxyfuel Combustion Background Oxy-combustion in a pulverized coal-fired power station produces a raw carbon dioxide (CO 2 ) product containing contaminants such as water vapor, oxygen, nitrogen, and argon from impurities in the oxygen used and any air leakage into the system. Acid gases are also produced as combustion products, such as sulfur oxides (SO

96

Sorbent Injection for Small ESP Mercury Control in Low Sulfur Eastern Bituminous Coal Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Sorbent InjectIon for Small eSP Sorbent InjectIon for Small eSP mercury control In low Sulfur eaStern bItumInouS coal flue GaS Background Full-scale field testing has demonstrated the effectiveness of activated carbon injection (ACI) as a mercury-specific control technology for certain coal-fired power plants, depending on the plant's coal feedstock and existing air pollution control device configuration. In a typical configuration, powdered activated carbon (PAC) is injected downstream of the plant's air heater and upstream of the existing particulate control device - either an electrostatic precipitator (ESP) or a fabric filter (FF). The PAC adsorbs the mercury from the combustion flue gas and is subsequently captured along with the fly ash in the ESP or FF. ACI can have some negative side

97

The Flakt-Hydro process: flue gas desulfurisation by use of seawater  

Science Journals Connector (OSTI)

ABB's seawater scrubbing process (the Flakt-Hydro process) for flue gas desulfurisation has recently triggered much interest among power producers because of its simple operating principle and high reliability. The process uses seawater to absorb and neutralise sulfur dioxide in flue gases. The absorbed gas is oxidised and returned to the ocean in the form it originated in the first place, namely as dissolved sulfate salts. The process uses the seawater downstream of the power plant condensers. This paper gives an introduction to the basic principle of the process and presents some of the recent power plant applications, namely at the Paiton Private Power Project, Phase 1 (2 ? 670 Mwe) in Indonesia and at the Shenzhen West Power Plant, Unit 2 (300 MWe) in China.

Wu Zhao Xia

1999-01-01T23:59:59.000Z

98

Membrane Process to Capture CO2 from Power Plant Flue Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Membrane Process to Capture CO Membrane Process to Capture CO 2 from Power Plant Flue Gas Background The U.S. Department of Energy's (DOE) Innovations for Existing Plants (IEP) Program is performing research to develop advanced technologies focusing on carbon dioxide (CO 2 ) emissions control for existing pulverized coal-fired plants. This new focus on post-combustion and oxy-combustion CO 2 emissions control technology, CO 2 compression, and beneficial reuse is in response to the priority for advanced

99

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

SciTech Connect (OSTI)

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

Eric P. Robertson

2007-09-01T23:59:59.000Z

100

Corrosion protection by means of rubber linings in a flue gas scrubber made of concrete  

SciTech Connect (OSTI)

Rubber linings have been applied as a corrosion protection measure for steel surfaces, particularly in the absorbers, in the flue gas desulfurization plants of a large number of power stations in Europe and have decidedly proven their effectiveness. The rubber linings applied consist of either precured and/or cold-curing rubber sheets. In the course of the past five to seven years, the eastern European states have also begun retro-fitting their existing power stations with flue gas desulfurization plants. As the first of its kind, a scrubber in the flue gas desulfurization plant of the Konin Power Station in Poland, which operates on the basis of the limestone-gypsum process, was constructed of concrete. In this case also, the corrosion protection measures implemented consisted in the application of a precured rubber lining on the basis of butyl rubber. A surface area measuring 1,500 m{sup 2} of the concrete absorber was protected by means of this corrosion protection system.

Fenner, J.; Matos, A.; Seiffert, W. [Keramchemie GmbH, Siershahn (Germany)

1998-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
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101

Coagulation/Flocculation Treatments for Flue-Gas-Derived Water from Oxyfuel Power Production with CO2 Capture  

Science Journals Connector (OSTI)

Coagulation/Flocculation Treatments for Flue-Gas-Derived Water from Oxyfuel Power Production with CO2 Capture ... The buffered solution is then sent back to the top of the tower, where it is sprayed into the upflowing oxyfuel gas stream, condensing and cleaning the ash-laden gas. ...

Sivaram Harendra; Danylo Oryshchyn; Thomas Ochs; Stephen Gerdemann; John Clark; Cathy Summers

2011-08-02T23:59:59.000Z

102

Compression Stripping of Flue Gas with Energy Recovery  

DOE Patents [OSTI]

A method of remediating and recovering energy from combustion products from a fossil fuel power plant having at least one fossil fuel combustion chamber, at least one compressor, at least one turbine, at least one heat exchanger and a source of oxygen. Combustion products including non-condensable gases such as oxygen and nitrogen and condensable vapors such as water vapor and acid gases such as SOX and NOX and CO2 and pollutants are produced and energy is recovered during the remediation which recycles combustion products and adds oxygen to support combustion. The temperature and/or pressure of the combustion products are changed by cooling through heat exchange with thermodynamic working fluids in the power generation cycle and/or compressing and/or heating and/or expanding the combustion products to a temperature/pressure combination below the dew point of at least some of the condensable vapors to condense liquid having some acid gases dissolved and/or entrained and/or directly condense acid gas vapors from the combustion products and to entrain and/or dissolve some of the pollutants while recovering sensible and/or latent heat from the combustion products through heat exchange between the combustion products and thermodynamic working fluids and/or cooling fluids used in the power generating cycle. Then the CO2, SO2, and H2O poor and oxygen enriched remediation stream is sent to an exhaust and/or an air separation unit and/or a turbine.

Ochs, Thomas L.; O'Connor, William K.

2005-05-31T23:59:59.000Z

103

Compression stripping of flue gas with energy recovery  

DOE Patents [OSTI]

A method of remediating and recovering energy from combustion products from a fossil fuel power plant having at least one fossil fuel combustion chamber, at least one compressor, at least one turbine, at least one heat exchanger and a source of oxygen. Combustion products including non-condensable gases such as oxygen and nitrogen and condensable vapors such as water vapor and acid gases such as SO.sub.X and NO.sub.X and CO.sub.2 and pollutants are produced and energy is recovered during the remediation which recycles combustion products and adds oxygen to support combustion. The temperature and/or pressure of the combustion products are changed by cooling through heat exchange with thermodynamic working fluids in the power generation cycle and/or compressing and/or heating and/or expanding the combustion products to a temperature/pressure combination below the dew point of at least some of the condensable vapors to condense liquid having some acid gases dissolved and/or entrained and/or directly condense acid gas vapors from the combustion products and to entrain and/or dissolve some of the pollutants while recovering sensible and/or latent heat from the combustion products through heat exchange between the combustion products and thermodynamic working fluids and/or cooling fluids used in the power generating cycle. Then the CO.sub.2, SO.sub.2, and H.sub.2 O poor and oxygen enriched remediation stream is sent to an exhaust and/or an air separation unit and/or a turbine.

Ochs, Thomas L. (Albany, OR); O'Connor, William K. (Lebanon, OR)

2005-05-31T23:59:59.000Z

104

Flue-gas sulfur-recovery plant for a multifuel boiler  

SciTech Connect (OSTI)

In October 1991, a Finnish fluting mill brought on stream a flue-gas desulfurization plant with an SO{sub 2} reduction capacity of 99%. The desulfurization plant enabled the mill to discontinue the use of its sulfur burner for SO{sub 2} production. The required makeup sulfur is now obtained in the form of sulfuric acid used by the acetic acid plant, which operates in conjunction with the evaporating plant. The mill`s sulfur consumption has decreased by about 6,000 tons/year (13.2 million lb/year) because of sulfur recycling.

Miettunen, J. [Tampella Power Inc., Tampere (Finland); Aitlahti, S. [Savon Sellu Oy, Kuopio (Finland)

1993-12-01T23:59:59.000Z

105

Advanced separation technology for flue gas cleanup. Quarterly technical report No. 8, [January--March 1994  

SciTech Connect (OSTI)

During the first quarter of 1994, we continued work on Tasks 2, 3, 4, 5, and 6. We also began work on Task 7. In Task 2, we incorporated 4.5% O{sub 2} into our simulated flue gas stream during this quarter`s NO{sub x}-absorption experiments. We also ran experiments using Cobalt (II)-phthalocyanine as an absorbing agent We observed higher absorption capacities when using this solution with the simulated flue gas containing O{sub 2}. In Task 3, we synthesized a few EDTA polymer analogs. We also began scaled up synthesis of Co(II)-phthalocyanine for use in Task 5. In Task 4, we performed experiments for measuring distribution coefficients (m{sub i}) Of SO{sub 2} between aqueous and organic phases. This was done using the liquor regenerating apparatus described in Task 6. In Task 5, we began working with Co(II)-phthalocyanine in the 301 fiber hollow fiber contactor. We also calculated mass transfer coefficients (K{sub olm}) for these runs, and we observed that the gas side resistance dominates mass transfer. In Task 6, in the liquor regeneration apparatus, we observed 90% recovery of SO{sub 2} by DMA from water used as the scrubbing solution. We also calculated the distribution of coefficients (m{sub i}). In Task 7, we established and began implementing a methodology for completing this task.

Bhown, A.S.; Alvarado, D.; Pakala, N.; Ventura, S. [SRI International, Menlo Park, CA (United States)] [SRI International, Menlo Park, CA (United States); Sirkar, K.K.; Majumdar, S.; Bhaumick, D. [New Jersey Inst. of Tech., Newark, NJ (United States)] [New Jersey Inst. of Tech., Newark, NJ (United States)

1994-03-01T23:59:59.000Z

106

Comparison of thermoelectric and permeation dryers for sulfur dioxide removal during sample conditioning of wet gas streams  

SciTech Connect (OSTI)

Flue gas conditioning for moisture removal is commonly performed for criteria pollutant measurements, in particular for extractive CEM systems at combustion sources. An implicit assumption is that conditioning systems specifically remove moisture without affecting pollutant and diluent concentrations. Gas conditioning is usually performed by passing the flue gas through a cold trap (Peltier or thermoelectric dryer) to remove moisture by condensation, which is subsequently extracted by a peristaltic pump. Many air pollutants are water-soluble and potentially susceptible to removal in a condensation dryer from gas interaction with liquid water. An alternative technology for gas conditioning is the permeation dryer, where the flue gas passes through a selectively permeable membrane for moisture removal. In this case water is transferred through the membrane while other pollutants are excluded, and the gas does not contact condensed liquid. Laboratory experiments were performed to measure the relative removal of a water-soluble pollutant (sulfur dioxide, SO{sub 2}) by the two conditioning techniques. A wet gas generating system was used to create hot, wet gas streams of known composition (15% and 30% moisture, balance nitrogen) and flow rate. Pre-heated SO{sub 2} was dynamically spiked into the wet stream using mass flow meters to achieve concentrations of 20, 50, and 100 ppm. The spiked gas was directed through a heated sample line to either a thermoelectric or a permeation conditioning system. Two gas analyzers (Western Research UV gas monitor, KVB/Analect FTIR spectrometer) were used to measure the SO{sub 2} concentration after conditioning. Both analytic methods demonstrated that SO{sub 2} is removed to a significantly greater extent by the thermoelectric dryer. These results have important implications for SO{sub 2} monitoring and emissions trading.

Dunder, T.A. [Entropy, Inc., Research Triangle Park, NC (United States). Research Div.; Leighty, D.A. [Perma Pure, Inc., Toms River, NJ (United States)

1997-12-31T23:59:59.000Z

107

ADVANCED FLUE GAS CONDITIONING AS A RETROFIT UPGRADE TO ENHANCE PM COLLECTION FROM COAL-FIRED ELECTRIC UTILITY BOILERS  

SciTech Connect (OSTI)

The U.S. Department of Energy and ADA Environmental Solutions are engaged in a project to develop commercial flue gas conditioning additives. The objective is to develop conditioning agents that can help improve particulate control performance of smaller or under-sized electrostatic precipitators on utility coal-fired boilers. The new chemicals will be used to control both the electrical resistivity and the adhesion or cohesivity of the fly ash. There is a need to provide cost-effective and safer alternatives to traditional flue gas conditioning with SO{sub 3} and ammonia. During this reporting quarter, installation of a liquid flue gas conditioning system was completed at the American Electric Power Conesville Plant, Unit 3. This plant fires a bituminous coal and has opacity and particulate emissions performance issues related to fly ash re-entrainment. Two cohesivity-specific additive formulations, ADA-44C and ADA-51, will be evaluated. In addition, ammonia conditioning will also be compared.

Kenneth E. Baldrey

2003-01-01T23:59:59.000Z

108

Potential Agricultural Uses of Flue Gas Desulfurization Gypsum in the Northern Great Plains  

SciTech Connect (OSTI)

Flue gas desulfurization gypsum (FGDG) is a byproduct from the combustion of coal for electrical energy production. Currently, FGDG is being produced by 15 electrical generating stations in Alabama, Florida, Indiana, Iowa, Kentucky, Ohio, North Carolina, South Carolina, Tennessee, Texas, and Wisconsin. Much of this byproduct is used in the manufacturing of wallboard. The National Network for Use of FGDG in Agriculture was initiated to explore alternative uses of this byproduct. In the northern Great Plains (North Dakota, South Dakota, and Montana), FGDG has the potential to be used as a Ca or S fertilizer, as an acid soil ameliorant, and for reclaiming or mitigating sodium-affected soils. Greater than 1.4 million Mg of FGDG could initially be used in these states for these purposes. Flue gas desulfurization gypsum can be an agriculturally important resource for helping to increase the usefulness of problem soils and to increase crop and rangeland production. Conducting beneficial use audits would increase the public awareness of this product and help identify to coal combustion electrical generating stations the agriculturally beneficial outlets for this byproduct.

DeSutter, T.M.; Cihacek, L.J. [North Dakota State University, Fargo, ND (United States). Department of Soil Science

2009-07-15T23:59:59.000Z

109

Flue gas cleaning with ammonia reduces SO{sub 2} emission  

SciTech Connect (OSTI)

This paper describes the technical and commercial development and basis for application in North America for wet flue gas desulfurization (FGD) of the AMASOX{reg_sign} (i.e. Ammonia Absorbs Sulfur Oxides) Process of Krupp Uhde (Germany) employing ammonia reagent. This process technology has been emerging slowly and stepwise over a twenty-year period in reaching the present stage of commercial applicability. The discussion herein considers the need for accommodating to and advantageously addressing the increasing number of applications with high and ultra-high flue-gas concentrations of SO{sub 2} at the boiler outlet accompanied by significant levels of other pollutants. Key measures in accomplishing this include use of important process innovations. This, as well, calls for the effective use, when applicable, of wet electrostatic precipitator mist-elimination means to gain low/minimum-opacity stack plume trailoff in wet scrubber use together with reduction of air toxics to low concentrations. With cost-effectiveness in electric utility service, detailed herein, superior to FGD processes commonly used to date in high-sulfur service, utilization of this technology is expanding. Important, potentially trend-setting types of powerplant applications of ammonia FGD are reviewed to identify foreseen market sectors and procurement trends that will at the same time serve to substantially broaden lowest-cost coal utilization.

Emish, G.J. [Krupp Wilputte Corp., Bridgeville, PA (United States); Schulte, W. [Krupp Uhde GmbH, Dortmund (Germany); Ellison, W. [Ellison Consultants, Monrovia, MD (United States)

1997-12-31T23:59:59.000Z

110

Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas  

SciTech Connect (OSTI)

The objective of this project is to demonstrate an innovative process to mineralize CO2 from flue gas directly to reactive carbonates and maximize the value and versatility of its beneficial use products. The program scope includes the design, construction, and testing of a CO2 Conversion to Material Products (CCMP) Pilot Demonstration Plant utilizing CO2 from the flue gas of a power production facility in Moss Landing, CA. This topical report covers Subphase 2a which is the design phase of pilot demonstration subsystems. Materials of construction have been selected and proven in both lab scale and prototype testing to be acceptable for the reagent conditions of interest. The target application for the reactive carbonate material has been selected based upon small-scale feasibility studies and the design of a continuous fiber board production line has been completed. The electrochemical cell architecture and components have been selected based upon both lab scale and prototype testing. The appropriate quality control and diagnostic techniques have been developed and tested along with the required instrumentation and controls. Finally the demonstrate site infrastructure, NEPA categorical exclusion, and permitting is all ready for the construction and installation of the new units and upgrades.

Devenney, Martin; Gilliam, Ryan; Seeker, Randy

2013-08-01T23:59:59.000Z

111

ADVANCED FLUE GAS CONDITIONING AS A RETROFIT UPGRADE TO ENHANCE PM COLLECTION FROM COAL-FIRED ELECTRIC UTILITY BOILERS  

SciTech Connect (OSTI)

The U.S. Department of Energy and ADA Environmental Solutions are engaged in a project to develop commercial flue gas conditioning additives. The objective is to develop conditioning agents that can help improve particulate control performance of smaller or under-sized electrostatic precipitators on utility coal-fired boilers. The new chemicals will be used to control both the electrical resistivity and the adhesion or cohesivity of the fly ash. There is a need to provide cost-effective and safer alternatives to traditional flue gas conditioning with SO{sub 3} and ammonia. During this reporting quarter, performance testing of flue gas conditioning was underway at the PacifiCorp Jim Bridger Power Plant. The product tested, ADA-43, was a combination resistivity modifier with cohesivity polymers. This represents the first long-term full-scale testing of this class of products. Modifications to the flue gas conditioning system at Jim Bridger, including development of alternate injection lances, was also undertaken to improve chemical spray distribution and to avoid spray deposition to duct interior surfaces. Also in this quarter, a firm commitment was received for another long-term test of the cohesivity additives. This plant fires a bituminous coal and has opacity and particulate emissions performance issues related to fly ash re-entrainment. Ammonia conditioning is employed here on one unit, but there is interest in liquid cohesivity additives as a safer alternative.

Kenneth E. Baldrey

2002-05-01T23:59:59.000Z

112

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million...  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3...

113

NITROGEN REMOVAL FROM NATURAL GAS  

SciTech Connect (OSTI)

The objective of this project was to develop a membrane process for the denitrogenation of natural gas. Large proven reserves in the Lower-48 states cannot be produced because of the presence of nitrogen. To exploit these reserves, cost-effective, simple technology able to reduce the nitrogen content of the gas to 4-5% is required. Technology applicable to treatment of small gas streams (below 10 MMscfd) is particularly needed. In this project membranes that selectively permeate methane and reject nitrogen in the gas were developed. Preliminary calculations show that a membrane with a methane/nitrogen selectivity of 3 to 5 is required to make the process economically viable. A number of polymer materials likely to have the required selectivities were evaluated as composite membranes. Polyacetylenes such as poly(1-trimethylsilyl-1-propyne) [PTMSP] and poly(4-methyl-2-pentyne) [PMP] had high selectivities and fluxes, but membranes prepared from these polymers were not stable, showing decreasing flux and selectivity during tests lasting only a few hours. Parel, a poly(propylene oxide allyl glycidyl ether) had a selectivity of 3 at ambient temperatures and 4 or more at temperatures of {minus}20 C. However, Parel is no longer commercially available, and we were unable to find an equivalent material in the time available. Therefore, most of our experimental work focused on silicone rubber membranes, which have a selectivity of 2.5 at ambient temperatures, increasing to 3-4 at low temperatures. Silicone rubber composite membranes were evaluated in bench-scale module tests and with commercial-scale, 4-inch-diameter modules in a small pilot plant. Over six days of continuous operation at a feed gas temperature of {minus}5 to {minus}10 C, the membrane maintained a methane/nitrogen selectivity of about 3.3. Based on the pilot plant performance data, an analysis of the economic potential of the process was prepared. We conclude that a stand-alone membrane process is the lowest-cost technology for small gas streams containing less than 10% nitrogen. The membrane process can recover more than 60-70% of the hydrocarbon content of the gas at a cost of $0.60-0.70/Mscfd. The capital cost of the process is about $100-200/Mscf. A number of small operators appear to be ready to use the technology if these costs can be demonstrated in the field. A second, and perhaps better, application of the technology is to combine the membrane process with a cryogenic process to treat large gas streams containing 10-20% nitrogen. The combination process achieves significant synergies. The membrane process performs a bulk separation of the gas, after which the cryogenic process treats the membrane residue (nitrogen-enriched) gas to recover more methane. Overall, hydrocarbon recoveries are greater than 95%. The capital cost of the combination process is lower than that of either process used alone and the processing costs are in the range $0.30-0.40/Mscf. This operating cost would be attractive to many gas producers. MTR is collaborating with a producer of cryogenic systems to further develop the combination process. A number of innovations in membrane process designs were made during the project; four U.S. patents covering various aspects of the technology were filed and issued.

K.A. Lokhandwala; M.B. Ringer; T.T. Su; Z. He; I. Pinnau; J.G. Wijmans; A. Morisato; K. Amo; A. DaCosta; R.W. Baker; R. Olsen; H. Hassani; T. Rathkamp

1999-12-31T23:59:59.000Z

114

ADVANCED FLUE GAS CONDITIONING AS A RETROFIT UPGRADE TO ENHANCE PM COLLECTION FROM COAL-FIRED ELECTRIC UTILITY BOILERS  

SciTech Connect (OSTI)

The U.S. Department of Energy and ADA Environmental Solutions are engaged in a project to develop commercial flue gas conditioning additives. The objective is to develop conditioning agents that can help improve particulate control performance of smaller or under-sized electrostatic precipitators on utility coal-fired boilers. The new chemicals will be used to control both the electrical resistivity and the adhesion or cohesivity of the fly ash. There is a need to provide cost-effective and safer alternatives to traditional flue gas conditioning with SO{sub 3} and ammonia. During this reporting quarter, performance testing of flue gas conditioning was completed at the PacifiCorp Jim Bridger Power Plant. The product tested, ADA-43, was a combination resistivity modifier with cohesivity polymers. The product was effective as a flue gas conditioner. However, ongoing problems with in-duct deposition resulting from the flue gas conditioning were not entirely resolved. Primarily these problems were the result of difficulties encountered with retrofit of an existing spray humidification system. Eventually it proved necessary to replace all of the original injection lances and to manually bypass the PLC-based air/liquid feed control. This yielded substantial improvement in spray atomization and system reliability. However, the plant opted not to install a permanent system. Also in this quarter, preparations continued for a test of the cohesivity additives at the American Electric Power Conesville Plant, Unit 3. This plant fires a bituminous coal and has opacity and particulate emissions performance issues related to fly ash re-entrainment. Ammonia conditioning is employed here on one unit, but there is interest in liquid cohesivity additives as a safer alternative.

Kenneth E. Baldrey

2002-07-01T23:59:59.000Z

115

Management of dry flue gas dsulfurization by-products in underground mines - an update  

SciTech Connect (OSTI)

In 1993, the U.S. produced about 100 million tons of coal combustion by-products (CCBs) primarily from conventional coal-fired boilers. The requirement to reduce SO{sub x} and NO{sub x} emissions to comply with the 1990 Clean Air Act Amendments (CAAA) force utilities to adopt advanced combustion and flue gas desulfurization (FGD) technologies, such as wet scrubbers, fluidized bed combustion (FBC), dry sorbent duct or furnace injection. These technologies will double to triple the amount of FGD by-products while only slightly increasing the amounts of conventional combustion residues, such as fly ash, bottom ash and boiler slag. This paper describes a program concerned with the underground disposal of combustion products in abandoned underground coal mines.

Chugh, Y.P.; Thomasson, E.M. [Southern Illinois Univ., Carbondale, IL (United States)

1996-09-01T23:59:59.000Z

116

The desulfurization of flue gas at the Mae Moh Power Plant Units 12 and 13  

SciTech Connect (OSTI)

As pollution of air, water and ground increasingly raises worldwide concern, the responsible national and international authorities establish and issue stringent regulations in order to maintain an acceptable air quality in the environment. In Thailand, the Electricity Generating Authority of Thailand (EGAT) takes full responsibility in environmental protection matters as well as in generating the electricity needed to supply the country`s very rapid power demand growth. Due to the rapidly increasing electricity demand of the country, EGAT had decided to install two further lignite-fired units of 300 MW each (Units 12 and 13) at the Mae Moh power generation station and they are now under construction. The arrangement and the capacity of all the power plant units are as shown. In 1989, EGAT started the work on the flue gas desulfurization system of Mae Moh power plant units 12 and 13 as planned. A study has been conducted to select the most suitable and most economical process for flue gas desulfurization. The wet scrubbing limestone process was finally selected for the two new units. Local limestone will be utilized in the process, producing a by-product of gypsum. Unfortunately, natural gypsum is found in abundance in Thailand, so the produced gypsum will be treated as landfill by mixing it with ash from the boilers of the power plants and then carrying it to the ash dumping area. The water from the waste ash water lake is utilized in the process as much as possible to minimize the requirement of service water, which is a limited resource. The Mae Moh power generation station is situated in the northern region of Thailand, 600 km north of Bangkok and about 30 km east of the town of Lampang, close to the Mae Moh lignite mine. Three lignite-fired units (Units 1-3) of 75 MW each, four units (Units 4-7) of 150 MW each and four units (Units 8-11) of 300 MW each are in operation.

Haemapun, C.

1993-12-31T23:59:59.000Z

117

Separation of flue-gas scrubber sludge into marketable products. Second year, second quarterly technical progress report, Quarter No. 6, December 1, 1994--February 28, 1995  

SciTech Connect (OSTI)

To reduce their sulfur emissions, many coal-fired electric power plants use wet flue-gas scrubbers. These scrubbers convert sulfur oxides into solid sulfate and sulfite sludge, which must then be disposed of. This sludge is a result of reacting limestone with sulfur dioxide to precipitate calcium sulfite and calcium sulfate. It consists of calcium sulfite (CaSO{sub 3}{sm_bullet}0.5H{sub 2}O), gypsum (CaSO{sub 4}{sm_bullet}2H{sub 2}O), and unreacted limestone (CaCO{sub 3}) or lime (Ca(OH){sub 2}), with miscellaneous objectionable impurities such as iron oxides, silica, and magnesium, sodium, and potassium oxides or salts. These impurities prevent many sludges from being utilized as a replacement for natural gypsum, and as a result they must be disposed of in landfills, which presents a serious disposal problem. This project is studying the characteristics of flue-gas scrubber sludges from several sources, which is necessary for the development of purification technologies which will make it possible to directly utilize scrubber sludges rather than landfilling them. This purification will consist of minimal-reagent froth flotation, using the surface properties of the particles of unreacted limestone to remove them and their associated impurities from the material, leaving a purified calcium sulfite/gypsum product.

KAwatra, S.K.; Eisele, T.C.

1995-03-01T23:59:59.000Z

118

Nitrogen Removal From Low Quality Natural Gas  

SciTech Connect (OSTI)

Natural gas provides more than one-fifth of all the primary energy used in the United States. It is especially important in the residential sector, where it supplies nearly half of all the energy consumed in U.S. homes. However, significant quantities of natural gas cannot be produced economically because its quality is too low to enter the pipeline transportation system without some type of processing, other than dehydration, to remove the undesired gas fraction. Such low-quality natural gas (LQNG) contains significant concentration or quantities of gas other than methane. These non- hydrocarbons are predominantly nitrogen, carbon dioxide, and hydrogen sulfide, but may also include other gaseous components. The nitrogen concentrations usually exceeds 4%. Nitrogen rejection is presently an expensive operation which can present uneconomic scenarios in the potential development of natural gas fields containing high nitrogen concentrations. The most reliable and widely used process for nitrogen rejection from natural gas consists of liquefying the feed stream using temperatures in the order of - 300{degrees}F and separating the nitrogen via fractionation. In order to reduce the gas temperature to this level, the gas is compressed, cooled by mullet-stream heat exchangers, and expanded to low pressure. Significant energy for compression and expensive materials of construction are required. Water and carbon dioxide concentrations must be reduced to levels required to prevent freezing. SRI`s proposed research involves screening new nitrogen selective absorbents and developing a more cost effective nitrogen removal process from natural gas using those compounds. The long-term objective of this project is to determine the technical and economical feasibility of a N{sub 2}2 removal concept based on complexation of molecular N{sub 2} with novel complexing agents. Successful development of a selective, reversible, and stable reagent with an appropriate combination of capacity and N{sub 2} absorption/desorption characteristics will allow selective separation of N{sub 2} from LQNG.

Alvarado, D.B.; Asaro, M.F.; Bomben, J.L.; Damle, A.S.; Bhown, A.S.

1997-10-01T23:59:59.000Z

119

CO2 separation from flue gas using hollow fiber membrane contactors  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Research on CO Research on CO 2 Separation from Flue Gas Prof. Mengxiang Fang State Key Laboratory of Clean Energy Utilization, Zhejiang University, China Global CO 2 Emissions Country CO 2 Emission (MtCO2) 1990 2003 2004 2010 USA 4,989 5,800 5,923 6,156 China 2,241 3,898 4,707 6,432 Russia 2,334 1,602 1,685 1,840 Japan 1,015 1,244 1,262 1,260 World 21,246 25,508 26,922 30,670 Source: Energy Information Administration/International Energy Outlook 2004 with High Oil Price Case CO 2 Emission in China Year Total Coal Petroleum Natural Gas Mt CO2 Mtc % Mtc % Mtc % 1990 2,241 1,886 84.2 325 14.5 30 1.34 2003 3,898 3,117 80.0 711 18.2 70 1.80 2004 4,707 3,809 80.9 816 17.3 83 1.76 2010 6,432 5,103 79.3 1,151 17.9 178 2.76 2015 7,376 5,946 80.6 1,184 16.1 246 3.33 Source: Energy Information Administration/International Energy Outlook 2004 with High Oil Price Case.

120

JV Task 5 - Evaluation of Residual Oil Fly Ash As A Mercury Sorbent For Coal Combustion Flue Gas  

SciTech Connect (OSTI)

The mercury adsorption capacity of a residual oil fly ash (ROFA) sample collected form Florida Power and Light Company's Port Everglades Power Plant was evaluated using a bituminous coal combustion flue gas simulator and fixed-bed testing protocol. A size-segregated (>38 {micro}g) fraction of ROFA was ground to a fine powder and brominated to potentially enhance mercury capture. The ROFA and brominated-ROFA were ineffective in capturing or oxidizing the Hg{sup 0} present in a simulated bituminous coal combustion flue gas. In contrast, a commercially available DARCO{reg_sign} FGD initially adsorbed Hg{sup 0} for about an hour and then catalyzed Hg{sup 0} oxidation to produce Hg{sup 2+}. Apparently, the unburned carbon in ROFA needs to be more rigorously activated in order for it to effectively capture and/or oxidize Hg{sup 0}.

Robert Patton

2006-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

Innovative Carbon Dioxide Sequestration from Flue Gas Using an In-Duct Scrubber Coupled with Alkaline Clay Mineralization  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Innovative Carbon Dioxide Sequestration Innovative Carbon Dioxide Sequestration from Flue Gas Using an In-Duct Scrubber Coupled with Alkaline Clay Mineralization Background The United States Department of Energy (DOE) is leading an effort to find novel approaches to reduce carbon dioxide (CO 2 ) emissions from industrial sources. The Industrial Carbon Capture and Sequestration (ICCS) program is funded by the American Recovery and Reinvestment Act (ARRA) to encourage development of processes that

122

Separation of Fine Particles from Gases in Wet Flue Gas Desulfurization System Using a Cascade of Double Towers  

Science Journals Connector (OSTI)

Separation of Fine Particles from Gases in Wet Flue Gas Desulfurization System Using a Cascade of Double Towers ... The authors thank the High-Tech Research and Development Program of China (No. 2008AA05Z306), the Natural Science Foundation of Jiangsu Province (No. BK2008283), and the Scientific Research Foundation of Graduate School of Southeast University for their financial support. ... with high performance by cascading packed columns. ...

Jingjing Bao; Linjun Yang; Shijuan Song; Guilong Xiong

2012-02-15T23:59:59.000Z

123

ADVANCED FLUE GAS CONDITIONING AS A RETROFIT UPGRADE TO ENHANCE PM COLLECTION FROM COAL-FIRED ELECTRIC UTILITY BOILERS  

SciTech Connect (OSTI)

The U.S. Department of Energy and ADA Environmental Solutions are engaged in a project to develop commercial flue gas conditioning additives. The objective is to develop conditioning agents that can help improve particulate control performance of smaller or under-sized electrostatic precipitators on utility coal-fired boilers. The new chemicals will be used to control both the electrical resistivity and the adhesion or cohesivity of the fly ash. There is a need to provide cost-effective and safer alternatives to traditional flue gas conditioning with SO{sub 3} and ammonia. During this reporting quarter, installation of a flue gas conditioning system was completed at PacifiCorp Jim Bridger Power Plant. Performance testing was underway. Results will be detailed in the next quarterly and subsequent technical summary reports. Also in this quarter, discussions were initiated with a prospective long-term candidate plant. This plant fires a bituminous coal and has opacity performance issues related to fly ash re-entrainment. Ammonia conditioning has been proposed here, but there is interest in liquid additives as a safer alternative.

Kenneth E. Baldrey

2002-01-01T23:59:59.000Z

124

ADVANCED FLUE GAS CONDITIONING AS A RETROFIT UPGRADE TO ENHANCE PM COLLECTION FROM COAL-FIRED ELECTRIC UTILITY BOILERS  

SciTech Connect (OSTI)

The U.S. Department of Energy and ADA Environmental Solutions are engaged in a project to develop commercial flue gas conditioning additives. The objective is to develop conditioning agents that can help improve particulate control performance of smaller or under-sized electrostatic precipitators on utility coal-fired boilers. The new chemicals will be used to control both the electrical resistivity and the adhesion or cohesivity of the fly ash. There is a need to provide cost-effective and safer alternatives to traditional flue gas conditioning with SO{sub 3} and ammonia. This quarterly report summarizes project activity for the period April-June, 2003. In this period there was limited activity and no active field trials. Results of ash analysis from the AEP Conesville demonstration were received. In addition, a site visit was made to We Energies Presque Isle Power Plant and a proposal extended for a flue gas conditioning trial with the ADA-51 cohesivity additive. It is expected that this will be the final full-scale evaluation on the project.

Kenneth E. Baldrey

2003-07-30T23:59:59.000Z

125

Separation of the components of flue-gas scrubber sludge by froth flotation  

SciTech Connect (OSTI)

To reduce their sulfur emissions, many coal-fired electric power plants use wet flue-gas scrubbers. These scrubbers convert sulfur oxides into solid sulfate and sulfite sludge, which must then be disposed of. Currently, the major markets for scrubber sludge are for manufacture of gypsum products, such as wallboard and plaster, and for cement. However, the quality of the raw sludge is often not high enough or consistent enough to satisfy manufacturers, and so the material is difficult to sell. Other markets, such as paper manufacture and plastics fillers, have even more stringent quality requirements and will not accept raw sludge at all. In the work described in this paper, several reagents have been examined to determine their ability to selectively improve the flotation of the unreacted limestone contaminant away from the desirable products (calcium sulfite and gypsum). The most success has been achieved using a cationic collector, which shows a higher selectivity between calcium sulfite and calcium carbonate than do the anionic collectors that were studied.

Kawatra, S.K.; Eisele, T.C. [Michigan Technological Univ., Houghton, MI (United States). Dept. of Metallurgical and Materials Engineering

1995-12-31T23:59:59.000Z

126

Heat exchanger design for thermoelectric electricity generation from low temperature flue gas streams .  

E-Print Network [OSTI]

??An air-to-oil heat exchanger was modeled and optimized for use in a system utilizing a thermoelectric generator to convert low grade waste heat in flue… (more)

Latcham, Jacob G. (Jacob Greco)

2009-01-01T23:59:59.000Z

127

Using coke-battery flue gas to dry coal batch before coking  

Science Journals Connector (OSTI)

The utilization of heat from coke-battery flue gases and other potential secondary energy resources in drying coal batch prior to coking is considered. The main factors that influence ... . The reduction in moist...

A. Ya. Eremin; V. G. Mishchikhin; S. G. Stakheev; R. R. Gilyazetdinov…

2011-03-01T23:59:59.000Z

128

Next Generation Pressurized Oxy-Coal Combustion: High Efficiency and No Flue Gas Recirculation  

SciTech Connect (OSTI)

The Gas Technology Institute (GTI) has developed a pressurized oxy-coal fired molten bed boiler (MBB) concept, in which coal and oxygen are fired directly into a bed of molten coal slag through burners located on the bottom of the boiler and fired upward. Circulation of heat by the molten slag eliminates the need for a flue gas recirculation loop and provides excellent heat transfer to steam tubes in the boiler walls. Advantages of the MBB technology over other boilers include higher efficiency (from eliminating flue gas recirculation), a smaller and less expensive boiler, modular design leading to direct scalability, decreased fines carryover and handling costs, smaller exhaust duct size, and smaller emissions control equipment sizes. The objective of this project was to conduct techno-economic analyses and an engineering design of the MBB project and to support this work with thermodynamic analyses and oxy-coal burner testing. Techno-economic analyses of GTI’s pressurized oxy-coal fired MBB technology found that the overall plant with compressed CO2 has an efficiency of 31.6%. This is a significant increase over calculated 29.2% efficiency of first generation oxy-coal plants. Cost of electricity (COE) for the pressurized MBB supercritical steam power plant with CO2 capture and compression was calculated to be 134% of the COE for an air-coal supercritical steam power plant with no CO2 capture. This compares positively with a calculated COE for first generation oxy-coal supercritical steam power plants with CO2 capture and compression of 164%. The COE for the MBB power plant is found to meet the U.S. Department of Energy (DOE) target of 135%, before any plant optimization. The MBB power plant was also determined to be simpler than other oxy-coal power plants with a 17% lower capital cost. No other known combustion technology can produce higher efficiencies or lower COE when CO2 capture and compression are included. A thermodynamic enthalpy and exergy analysis found a number of modifications and adjustments that could provide higher efficiency and better use of available work. Conclusions from this analysis will help guide the analyses and CFD modeling in future process development. The MBB technology has the potential to be a disruptive technology that will enable coal combustion power plants to be built and operated in a cost effective way, cleanly with no carbon dioxide emissions. A large amount of work is needed to quantify and confirm the great promise of the MBB technology. A Phase 2 proposal was submitted to DOE and other sponsors to address the most critical MBB process technical gaps. The Phase 2 proposal was not accepted for current DOE support.

Rue, David

2013-09-30T23:59:59.000Z

129

CO{sub 2} Capture from Flue Gas Using Solid Molecular Basket Sorbents  

SciTech Connect (OSTI)

The objective of this project is to develop a new generation of solid, regenerable polymeric molecular basket sorbent (MBS) for more cost-efficient capture and separation of CO{sub 2} from flue gas of coal-fired power plants. The primary goal is to develop a cost-effective MBS sorbent with better thermal stability. To improve the cost-effectiveness of MBS, we have explored commercially available and inexpensive support to replace the more expensive mesoporous molecular sieves like MCM-41 and SBA- 15. In addition, we have developed some advanced sorbent materials with 3D pore structure such as hexagonal mesoporous silica (HMS) to improve the CO{sub 2} working capacity of MBS, which can also reduce the cost for the whole CO{sub 2} capture process. During the project duration, the concern regarding the desorption rate of MBS sorbents has been raised, because lower desorption rate increases the desorption time for complete regeneration of the sorbent which in turn leads to a lower working capacity if the regeneration time is limited. Thus, the improvement in the thermal stability of MBS became a vital task for later part of this project. The improvement in the thermal stability was performed via increasing the polymer density either using higher molecular weight PEI or PEI cross-linking with an organic compound. Moreover, we have used the computational approach to estimate the interaction of CO{sub 2} with different MBSs for the fundamental understanding of CO{sub 2} sorption, which may benefit the development, design and modification of the sorbents and the process.

Fillerup, Eric; Zhang, Zhonghua; Peduzzi, Emanuela; Wang, Dongxiang; Guo, Jiahua; Ma, Xiaoliang; Wang, Xiaoxing; Song, Chunshan

2012-08-31T23:59:59.000Z

130

Flue gas conditioning for improved particle collection in electrostatic precipitators. Quarterly technical report, October 1--December 31, 1993  

SciTech Connect (OSTI)

The initial pilot-scale testing of two additives was completed at CONSOL`s research coal combustor. The results and conclusions from this test series and subsequent analysis of the data are presented in this report. Table 1 summarizes the conditions tested. During the tests, the research combustor was firing a medium-sulfur coal. The combustor had recently been retrofitted with low-NOx burners for a DOE Clean Coal test program. Operation of the low-NOx burners required a reduced flow rate in the combustor, resulting in lower flow and velocity in the ESP. A comprehensive baseline condition was tested, followed by initial screening runs for several additives. It was discovered that the flyash exhibited properties characteristic of a high-resistivity ash. In-situ measurements at the ESP inlet confirmed that the resistivity was in the 10{sup 10} -- 10{sup 12} ohm-cm range. In addition, the ESP plate rappers were not able to remove ash buildup on the first section during normal operation. Power off rapping was periodically required to fully clean the plates; this is a clear indication of high-resistivity conditions. Since the major benefit of ESP additives will be to reduce reentrainment at low to midrange resistivity, this operating condition was undesirable for performance testing. It was decided to continue the program with SO{sub 3} conditioning of the flue gas to reduce particle resistivity. It was also decided to operate with two rather than three electrical fields energized. By reducing the ESP collection area, it was hoped that it would be easier to measure changes in ESP performance and to see an immediate indication of the effectiveness Of SO{sub 3} conditioning. The ESP was reconfigured with two electrical sections energized and SO{sub 3} conditioning at a rate of approximately 20 ppM. An additional baseline was run, followed by extended tests with two additives referred to in this report as Additive ``C`` and Additive ``D.``

Durham, M.D.; Baldrey, K.E.

1994-01-12T23:59:59.000Z

131

ADVANCED FLUE GAS CONDITIONING AS A RETROFIT UPGRADE TO ENHANCE PM COLLECTION FROM COAL-FIRED ELECTRIC UTILITY BOILERS  

SciTech Connect (OSTI)

The U.S. Department of Energy and ADA Environmental Solutions are engaged in a project to develop commercial flue gas conditioning additives. The objective is to develop conditioning agents that can help improve particulate control performance of smaller or under-sized electrostatic precipitators on utility coal-fired boilers. The new chemicals will be used to control both the electrical resistivity and the adhesion or cohesivity of the fly ash. There is a need to provide cost-effective and safer alternatives to traditional flue gas conditioning with SO{sub 3} and ammonia. During this reporting quarter, further laboratory-screening tests of additive formulations were completed. For these tests, the electrostatic tensiometer method was used for determination of fly ash cohesivity. Resistivity was measured for each screening test with a multi-cell laboratory fly ash resistivity furnace constructed for this project. Also during this quarter chemical formulation testing was undertaken to identify stable and compatible resistivity/cohesivity liquid products.

Kenneth E. Baldrey

2001-09-01T23:59:59.000Z

132

ADVANCED FLUE GAS CONDITIONING AS A RETROFIT UPGRADE TO ENHANCE PM COLLECTION FROM COAL-FIRED ELECTRIC UTILITY BOILERS  

SciTech Connect (OSTI)

The U.S. Department of Energy and ADA Environmental Solutions are engaged in a project to develop commercial flue gas conditioning additives. The objective is to develop conditioning agents that can help improve particulate control performance of smaller or under-sized electrostatic precipitators on utility coal-fired boilers. The new chemicals will be used to control both the electrical resistivity and the adhesion or cohesivity of the fly ash. There is a need to provide cost-effective and safer alternatives to traditional flue gas conditioning with SO{sub 3} and ammonia. During this reporting quarter, two cohesivity-specific additive formulations, ADA-44C and ADA-51, were evaluated in a full-scale trial at the American Electric Power Conesville plant. Ammonia conditioning was also evaluated for comparison. ADA-51 and ammonia conditioning significantly reduced rapping and non-rapped particulate re-entrainment based on stack opacity monitor data. Based on the successful tests to date, ADA-51 will be evaluated in a long-term test.

Kenneth E. Baldrey

2003-02-01T23:59:59.000Z

133

Energy and Economic Analysis of the CO2 Capture from Flue Gas of Combined Cycle Power Plants  

Science Journals Connector (OSTI)

Abstract Carbon capture and storage is considered as one of the key strategies for reducing the emissions of carbon dioxide from power generation facilities. Although post-combustion capture via chemical absorption is now a mature technology, the separation of CO2 from flue gases shows many issues, including the solvent degradation and the high regeneration energy requirement, that in turn reduces the power plant performances. Focusing on a triple pressure and reheat combined cycle with exhaust gas recirculation, this paper aims to evaluate the potential impacts of integrating a post-combustion capture system, based on an absorption process with monoethanolamine solvent. Energy and economic performances of the integrated system are evaluated varying the exhaust gas recirculation fraction and the CO2 capture ratio. The different configurations examined are then compared in terms of efficiency and rated capacity of the integrated system, as well as considering the cost of electricity generated and the cost of CO2 avoided.

Maura Vaccarelli; Roberto Carapellucci; Lorena Giordano

2014-01-01T23:59:59.000Z

134

Oil and Gas- Leases to remove or recover (Pennsylvania)  

Broader source: Energy.gov [DOE]

This act states that a lease or agreement conveying the right to remove or recover oil, natural gas or gas of any other designation from lessor to lessee shall not be valid if such lease does not...

135

Capture of Carbon Dioxide from Air and Flue Gas in the Alkylamine-Appended Metal-Organic Framework mmen-Mg2(dobpdc)  

E-Print Network [OSTI]

Capture of Carbon Dioxide from Air and Flue Gas in the Alkylamine- Appended Metal-Organic Framework, stationary sources like coal-fired power plants, carbon capture and sequestration (CCS) has been proposed.4 viable absorbents for carbon capture under the aforementioned conditions, and they are presently used

136

NETL: Gasification Systems - Warm Gas Multi-Contaminant Removal System  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Warm Gas Multi-Contaminant Removal System Warm Gas Multi-Contaminant Removal System Project Number: DE-SC00008243 TDA Research, Inc. is developing a high-capacity, low-cost sorbent that removes anhydrous ammonia (NH3), mercury (Hg), and trace contaminants from coal- and coal/biomass-derived syngas. The clean-up system will be used after the bulk warm gas sulfur removal step, and remove NH3 and Hg in a regenerable manner while irreversibly capturing all other trace metals (e.g., Arsenic, Selenium) reducing their concentrations to sub parts per million (ppm) levels. Current project plans include identifying optimum chemical composition and structure that provide the best sorbent performance for removing trace contaminants, determining the effect of operating parameters, conducting multiple-cycle experiments to test the life of the sorbent for NH3 and Hg removal, and conducting a preliminary design of the sorbent reactor.

137

Recovery of Water from Boiler Flue Gas Using Condensing Heat Exchangers ProMIS/Project No.: DE-NT0005648  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Edward Levy Edward Levy Principal Investigator Director, Lehigh University Energy Research Center RecoveRy of WateR fRom BoileR flue Gas usinG condensinG Heat excHanGeRs PRomis/PRoject no.: de-nt0005648 Background As the United States' population grows and demand for electricity and water increases, power plants located in some parts of the country will find it increasingly difficult to obtain the large quantities of water needed to maintain operations. Most of the water used in a thermoelectric power plant is used for cooling, and the U.S. Department of Energy (DOE) has been focusing on possible techniques to reduce the amount of fresh water needed for cooling. Many coal-fired power plants operate with stack temperatures in the 300 °F range to minimize fouling and corrosion problems due to sulfuric acid condensation and to

138

Flue gas desulfurization sludge: establishment of vegetation on ponded and soil-applied waste. Final report January 1977-September 1981  

SciTech Connect (OSTI)

The report gives results of research to identify and evaluate forms of vegetation and methods of their establishment for reclaiming retired flue gas desulfurization sludge ponds. Also studied were the soil liming value of limestone scrubber sludge (LSS) and plant uptake and percolation losses of some chemical nutrients in the sludge. Several vegetation schemes were evaluated between 1977 and 1982 for covering and stabilizing LSS at Colbert Steam Plant, Cherokee, AL, and Shawnee Steam Plant, Paducah, KY. Eleven tree and 10 grass or legume species were tested for adaptability and survival when planted directly in LSS or in LSS amended with soil, municipal sewage sludge, or standard potting mix. Other studies indicated that LSS apparently has sufficient unreacted limestone to be a satisfactory soil liming agent.

Giordano, P.M.; Mays, D.A.; Soileau, J.M.

1984-01-01T23:59:59.000Z

139

ADVANCED FLUE GAS CONDITIONING AS A RETROFIT UPGRADE TO ENHANCE PM COLLECTION FROM COAL-FIRED ELECTRIC UTILITY BOILERS  

SciTech Connect (OSTI)

ADA Environmental Solutions (ADA-ES) has successfully completed a research and development program granted by the Department of Energy National Energy Technology Laboratory (NETL) to develop a family of non-toxic flue gas conditioning agents to provide utilities and industries with a cost-effective means of complying with environmental regulations on particulate emissions and opacity. An extensive laboratory screening of potential additives was completed followed by full-scale trials at four utility power plants. The developed cohesivity additives have been demonstrated on a 175 MW utility boiler that exhibited poor collection of unburned carbon in the electrostatic precipitator. With cohesivity conditioning, opacity spiking caused by rapping reentrainment was reduced and total particulate emissions were reduced by more than 30%. Ammonia conditioning was also successful in reducing reentrainment on the same unit. Conditioned fly ash from the process is expected to be suitable for dry or wet disposal and for concrete admixture.

C. Jean Bustard

2003-12-01T23:59:59.000Z

140

Recycling of Flue Gas Desulfurization residues in gneiss based hot mix asphalt: Materials characterization and performances evaluation  

Science Journals Connector (OSTI)

Abstract On the one hand, huge amount of Flue Gas Desulfurization (FGD) residues, produced during scrubbing flue gas, is discarded as solid waste. Such solid waste would cause serious environmental problems. One the other hand, high quality aggregates, such as limestone and basalt, are running out due to the rapid development of highway construction. Ungraded aggregates such as gneiss are therefore considered in China to replace the high quality aggregates. The application of FGD residues as a filler in gneiss based asphalt mixture has benefits both in environmental and economic sides. The main objective of this research was to visualize the raw materials characterization and evaluate the effect of FGD residues on the performance of gneiss based asphalt mixture. X-ray diffraction (XRD), X-ray fluorescence (XRF), Scanning Electron Microscope (SEM), Differential Scanning Calorimetric & Thermal gravimetric (DSC–TG) were used to investigate the features of raw materials. The performance of gneiss based asphalt mixture including high-temperature deformation resistance, low-temperature crack resistance and moisture-induced damage resistance were evaluated. Dynamic creep test, three-point bending test, Retained Marshall Stability (RMS), Tensile Strength Ratio (TSR), Indirect Tensile (IDT) strength and Resilient Modulus (MR) test were conducted and analyzed. Dissipated Creep Strain Energy to fracture (DCSEf) ratio, fracture energy and model analysis were also used to evaluate moisture resistance, crack resistance and deformation resistance of asphalt mixture respectively. Research results indicate that FGD residues can partly improve the moisture resistance and crack resistance of gneiss asphalt mixture, while it might worse the high-temperature deformation resistance.

Zongwu Chen; Shaopeng Wu; Fuzhou Li; Juyong Chen; Zhehuan Qin; Ling Pang

2014-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

Development of Fly Ash Derived Sorbents to Capture CO2 from Flue Gas of Power Plants  

SciTech Connect (OSTI)

This research program focused on the development of fly ash derived sorbents to capture CO{sub 2} from power plant flue gas emissions. The fly ash derived sorbents developed represent an affordable alternative to existing methods using specialized activated carbons and molecular sieves, that tend to be very expensive and hinder the viability of the CO{sub 2} sorption process due to economic constraints. Under Task 1 'Procurement and characterization of a suite of fly ashes', 10 fly ash samples, named FAS-1 to -10, were collected from different combustors with different feedstocks, including bituminous coal, PRB coal and biomass. These samples presented a wide range of LOI value from 0.66-84.0%, and different burn-off profiles. The samples also spanned a wide range of total specific surface area and pore volume. These variations reflect the difference in the feedstock, types of combustors, collection hopper, and the beneficiation technologies the different fly ashes underwent. Under Task 2 'Preparation of fly ash derived sorbents', the fly ash samples were activated by steam. Nitrogen adsorption isotherms were used to characterize the resultant activated samples. The cost-saving one-step activation process applied was successfully used to increase the surface area and pore volume of all the fly ash samples. The activated samples present very different surface areas and pore volumes due to the range in physical and chemical properties of their precursors. Furthermore, one activated fly ash sample, FAS-4, was loaded with amine-containing chemicals (MEA, DEA, AMP, and MDEA). The impregnation significantly decreased the surface area and pore volume of the parent activated fly ash sample. Under Task 3 'Capture of CO{sub 2} by fly ash derived sorbents', sample FAS-10 and its deashed counterpart before and after impregnation of chemical PEI were used for the CO{sub 2} adsorption at different temperatures. The sample FAS-10 exhibited a CO{sub 2} adsorption capacity of 17.5mg/g at 30 C, and decreases to 10.25mg/g at 75 C, while those for de-ashed counterpart are 43.5mg/g and 22.0 mg/g at 30 C and 75 C, respectively. After loading PEI, the CO{sub 2} adsorption capacity increased to 93.6 mg/g at 75 C for de-ashed sample and 62.1 mg/g at 75 C for raw fly ash sample. The activated fly ash, FAS-4, and its chemical loaded counterparts were tested for CO{sub 2} capture capacity. The activated carbon exhibited a CO{sub 2} adsorption capacity of 40.3mg/g at 30 C that decreased to 18.5mg/g at 70 C and 7.7mg/g at 120 C. The CO{sub 2} adsorption capacity profiles changed significantly after impregnation. For the MEA loaded sample the capacity increased to 68.6mg/g at 30 C. The loading of MDEA and DEA initially decreased the CO{sub 2} adsorption capacity at 30 C compared to the parent sample but increased to 40.6 and 37.1mg/g, respectively, when the temperature increased to 70 C. The loading of AMP decrease the CO{sub 2} adsorption capacity compared to the parent sample under all the studied temperatures. Under Task 4 'Comparison of the CO{sub 2} capture by fly ash derived sorbents with commercial sorbents', the CO{sub 2} adsorption capacities of selected activated fly ash carbons were compared to commercial activated carbons. The CO{sub 2} adsorption capacity of fly ash derived activated carbon, FAS-4, and its chemical loaded counterpart presented CO{sub 2} capture capacities close to 7 wt%, which are comparable to, and even better than, the published values of 3-4%.

M. Mercedes Maroto-Valer; John M. Andresen; Yinzhi Zhang; Zhe Lu

2003-12-31T23:59:59.000Z

142

Method for removing particulate matter from a gas stream  

DOE Patents [OSTI]

Particulate matter is removed from a stream of pressurized gas by directing the stream of gas upwardly through a bed of porous material, the porous bed being held in an open ended container and at least partially submerged in liquid. The passage of the gas through the porous bed sets up a circulation in the liquid which cleans the particulate matter from the bed.

Postma, Arlin K. (Benton City, WA)

1984-01-01T23:59:59.000Z

143

Adsorption separation of CO2 from simulated flue gas mixtures by novel CO2 ''molecular basket'' adsorbents  

Science Journals Connector (OSTI)

Adsorption separation of CO2 from simulated flue gas mixtures containing CO2, O2, and N2 by using a novel CO2 ''molecular basket'' adsorbent was investigated in a flow adsorption separation system. The novel CO2 ''molecular basket'' adsorbents were developed by synthesising mesoporous molecular sieve MCM-41 and modifying it with polyethylenimine (PEI). The influence of operation conditions, including feed flow rate, temperature, feed CO2 concentration, and sweep gas flow rate, on the CO2 adsorption/desorption separation performance and CO2 breakthrough were examined. The CO2 adsorption capacity was 91.0 ml (STP)/g-PEI, which was 27 times higher than that of the MCM-41 alone. Further, the adsorbent showed separation selectivity of greater than 1000 for CO2/N2 ratio and approximately 180 for CO2/O2, which are significantly higher than those of the MCM-41, zeolites, and activated carbons. Cyclic adsorption/desorption measurements showed that the CO2 ''molecular basket'' adsorbent was stable at 75°C. However, the CO2 ''molecular basket'' adsorbent was not stable when the operation temperature was higher than 100°C.

Xiaochun Xu; Chunshan Song; John M. Andresen; Bruce G. Miller; Alan W. Scaroni

2004-01-01T23:59:59.000Z

144

Fundamental mechanisms in flue gas conditioning. Topical report No. 2, Literature review and assembly of theories on the interactions of ash and conditioning agents  

SciTech Connect (OSTI)

The overall goal of this research project is to formulate a mathematical model of flue gas conditioning. This model will be based on an understanding of why ask properties, such as cohesivity and resistivity, are changed by conditioning. Such a model could serve as a component of the performance models of particulate control devices where flue gas conditioning is used. There are two specific objectives of this research project, which divide the planned research into two main parts. One part of the project is designed to determine how ash particles are modified by interactions with sorbent injection processes and to describe the mechanisms by which these interactions affect fine particle collection. The objective of the other part of the project is to identify the mechanisms by which conditioning agents, including chemically active compounds, modify the key properties of fine fly ash particles.

Bush, P.V.; Snyder, T.R.

1992-01-09T23:59:59.000Z

145

Application of a low pressure economizer for waste heat recovery from the exhaust flue gas in a 600 MW power plant  

Science Journals Connector (OSTI)

This paper presents a case study of recovering the waste heat of the exhaust flue gas before entering a flue gas desulphurizer (FGD) in a 600 MW power plant. This waste heat can be recovered by installing a low pressure economizer (LPE) to heat the condensed water which can save the steam extracted from the steam turbine for heating the condensed water and then extra work can be obtained. The energy and water savings and the reduction of CO2 emission resulted from the LPE installation are assessed for three cases in a 600 MW coal-fired power plant with wet stack. Serpentine pipes with quadrate finned extensions are selected for the LPE heat exchanger which has an overall coefficient of heat transfer of 37 W/m2·K and the static pressure loss of 781 Pa in the optimized case. Analysis results show that it is feasible to install \\{LPEs\\} in the exhaust flue gas system between the pressurizing fan and the FGD, which has little negative impacts on the unit. The benefits generated include saving of standard coal equivalent (SCE) at 2–4 g/(kW·h) and saving of water at 25–35 t/h under full load operation with corresponding reduction of CO2 emission.

Chaojun Wang; Boshu He; Shaoyang Sun; Ying Wu; Na Yan; Linbo Yan; Xiaohui Pei

2012-01-01T23:59:59.000Z

146

Mercury Emission and Removal of a 135MW CFB Utility Boiler  

Science Journals Connector (OSTI)

To evaluate characteristic of the mercury emission and removal from a circulating fluidized bed (CFB) boiler, a representative 135 MW CFB utility boiler was selected to take the ... is of majority in flue gas of ...

Y. F. Duan; Y. Q. Zhuo; Y. J. Wang; L. Zhang…

2010-01-01T23:59:59.000Z

147

Enhanced Elemental Mercury Removal from Coal-fired Flue Gas by Sulfur-chlorine Compounds  

E-Print Network [OSTI]

III T; Murphy J T. DOE/NETL’s Phase II Mercury ControlFired Power Plants, DOE/NETL Mercury R&D Program Review,

Miller, Nai-Qiang Yan-Zan Qu Yao Chi Shao-Hua Qiao Ray Dod Shih-Ger Chang Charles

2008-01-01T23:59:59.000Z

148

DOE/FETC/TR--98-01 SORBENTS FOR MERCURY REMOVAL FROM FLUE GAS  

Office of Scientific and Technical Information (OSTI)

in the Analysis of Mercury in Air. Paper presented at the 66th Annual Meeting of the Air Pollution Control Association, June 1973. 45 Arizona Instrument Company, Manual for...

149

Flue Gas Purification Utilizing SOx/NOx Reactions During Compression of CO{sub 2} Derived from Oxyfuel Combustion  

SciTech Connect (OSTI)

The United States wishes to decrease foreign energy dependence by utilizing the country’s significant coal reserves, while stemming the effects of global warming from greenhouse gases. In response to these needs, Air Products has developed a patented process for the compression and purification of the CO{sub 2} stream from oxyfuel combustion of pulverized coal. The purpose of this project was the development and performance of a comprehensive experimental and engineering evaluation to determine the feasibility of purifying CO{sub 2} derived from the flue gas generated in a tangentially fired coal combustion unit operated in the oxy-combustion mode. Following the design and construction of a 15 bar reactor system, Air Products conducted two test campaigns using the slip stream from the tangentially fired oxy-coal combustion unit. During the first test campaign, Air Products evaluated the reactor performance based on both the liquid and gaseous reactor effluents. The data obtained from the test run has enabled Air Products to determine the reaction and mass transfer rates, as well as the effectiveness of the reactor system. During the second test campaign, Air Products evaluated reactor performance based on effluents for different reactor pressures, as well as water recycle rates. Analysis of the reaction equations indicates that both pressure and water flow rate affect the process reaction rates, as well as the overall reactor performance.

Fogash, Kevin

2010-09-30T23:59:59.000Z

150

Flue Gas Perification Utilizing SOx/NOx Reactions During Compression of CO2 Derived from Oxyfuel Combustion  

SciTech Connect (OSTI)

The United States wishes to decrease foreign energy dependence by utilizing the country’s significant coal reserves, while stemming the effects of global warming from greenhouse gases. In response to these needs, Air Products has developed a patented process for the compression and purification of the CO2 stream from oxyfuel combustion of pulverized coal. The purpose of this project was the development and performance of a comprehensive experimental and engineering evaluation to determine the feasibility of purifying CO2 derived from the flue gas generated in a tangentially fired coal combustion unit operated in the oxy-combustion mode. Following the design and construction of a 15 bar reactor system, Air Products conducted two test campaigns using the slip stream from the tangentially fired oxy-coal combustion unit. During the first test campaign, Air Products evaluated the reactor performance based on both the liquid and gaseous reactor effluents. The data obtained from the test run has enabled Air Products to determine the reaction and mass transfer rates, as well as the effectiveness of the reactor system. During the second test campaign, Air Products evaluated reactor performance based on effluents for different reactor pressures, as well as water recycle rates. Analysis of the reaction equations indicates that both pressure and water flow rate affect the process reaction rates, as well as the overall reactor performance.

Kevin Fogash

2010-09-30T23:59:59.000Z

151

Optimization and heat integration of hollow fiber based thermal swing adsorption process for CO2 capture from flue gas  

Science Journals Connector (OSTI)

Abstract This work studies the optimization of a hollow fiber contactor operated in a rapid temperature swing adsorption (RTSA) mode for CO2 capture from flue gas. A hollow fiber contactor enables rapid heat and mass transfer and an efficient heat integration whereby parasitic loads on power plants can be reduced significantly compared to the traditional thermal swing adsorption processes. In this paper we employ a dynamic optimization strategy to predict the optimal operating conditions of a hollow fiber RTSA process for different process design objectives. The objective function considered was to maximize the feed throughput of the process with constraints for the required CO2 purity and recovery. Furthermore, the external heat and cold utilities must be minimized. The optimization requires a dynamic heat integration i.e. redistributing the hot and cold stream outlet between different parts of a cycle which is challenging and unconventional. This has been performed using a binary decision variable which switches the outlet water stream between hot and cold tanks. We also show that a multi- objective optimization approach can be employed to determine the optimal trade-off between heat duty and process throughput. Optimization was performed using a single discretization approach within gPROMS.

Subramanian Swernath; Fateme Rezaei; Jayashree Kalyanaraman; Ryan. P. Lively; Matthew J. Realff; Yoshiaki Kawajiri

2014-01-01T23:59:59.000Z

152

Management of dry flue gas desulfurization by-products in underground mines. Quarterly report, April 1--June 30, 1996  

SciTech Connect (OSTI)

On September 30, 1993, the US Department of Energy - Morgantown Energy Technology Center (DOE-METC) and Southern Illinois University at Carbondale (SIUC) entered into a cooperative research agreement entitled {open_quotes}Management of Dry Flue Gas Desulfurization By-Products in Underground Mines{close_quotes} (DE-FC21-93MC30252). Under the agreement Southern Illinois University at Carbondale will develop and demonstrate two technologies for the placement of coal combustion residues in abandoned underground coal mines, and will assess the environmental impact of these technologies for the management of coal combustion by-products. The two technologies for the underground placement that will be developed and demonstrated are: (1) pneumatic placement, using virtually dry materials, and (2) hydraulic placement, using a {open_quotes}paste{close_quotes} mixture of materials with about 70% solids. Phase II of the overall program began April 1, 1996. The principal objective of Phase II is to develop and fabricate the equipment for placing the coal combustion by-products underground, and to conduct a demonstration of the technologies on the surface. Therefore, this quarter has been largely devoted to developing specifications for equipment components, visiting fabrication plants throughout Southern Illinois to determine their capability for building the equipment components in compliance with the specifications, and delivering the components in a timely manner.

NONE

1997-05-01T23:59:59.000Z

153

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

DOE Patents [OSTI]

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.

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

2014-10-07T23:59:59.000Z

154

Advances of flue gas desulfurization technology for coal-fired boilers and strategies for sulfur dioxide pollution prevention in China  

SciTech Connect (OSTI)

Coal is one of the most important kinds of energy resources at the present time and in the immediate future in China. Sulfur dioxide resulting from combustion of coal is one of the principle pollutants in the air. Control of SO{sub 2} discharge is still a major challenge for environmental protection in developing China. In this paper, research, development and application of technology of flue gas desulfurization (FGD) for coal-fired boilers in China will be reviewed with emphasis on cost-effective technology, and the development trends of FGD technology, as well as the strategy for SO{sub 2} discharge control in China, will be analyzed. A practical technology for middle-small-sized boilers developed by the primary author and the field investigation results will also be presented. At present, there are four major kinds of FGD technologies that are practical to be applied in China for their cost-effectiveness and efficiency to middle-small-sized boilers. An important development trend of the FGD technology for middle-small-sized boilers for the next decade is improvement of the existing cost-effective wet-type FGD technology, and in the future it will be the development of dry-type FGD technology. For middle-sized generating boilers, the development direction of the FGD technology is the spraying and drying process. For large-sized generating boilers, the wet-type limestone-plaster process will still be applied in the immediate future, and dry-type FGD technologies, such as ammonia with electron beam irradiation, will be developed in the future. State strategies for the control of SO{sub 2} discharge will involve the development and popularization of efficient coal-fired devices, extension of gas coal and liquefied coal, spreading coal washing, and centralized heating systems.

Yang, C.; Zeng, G.; Li, G.; Qiu, J.

1999-07-01T23:59:59.000Z

155

Process for off-gas particulate removal and apparatus therefor  

DOE Patents [OSTI]

In the event of a breach in the off-gas line of a melter operation requiring closure of the line, a secondary vessel vent line is provided with a particulate collector utilizing atomization for removal of large particulates from the off-gas. The collector receives the gas containing particulates and directs a portion of the gas through outer and inner annular channels. The collector further receives a fluid, such as water, which is directed through the outer channel together with a second portion of the particulate-laden gas. The outer and inner channels have respective ring-like termination apertures concentrically disposed adjacent one another on the outer edge of the downstream side of the particulate collector. Each of the outer and inner channels curves outwardly away from the collector`s centerline in proceeding toward the downstream side of the collector. Gas flow in the outer channel maintains the fluid on the channel`s wall in the form of a ``wavy film,`` while the gas stream from the inner channel shears the fluid film as it exits the outer channel in reducing the fluid to small droplets. Droplets formed by the collector capture particulates in the gas stream by one of three mechanisms: impaction, interception or Brownian diffusion in removing the particulates. The particulate-laden droplets are removed from the fluid stream by a vessel vent condenser or mist eliminator. 4 figs.

Carl, D.E.

1997-10-21T23:59:59.000Z

156

SYNTHESIS AND CHARACTERIZATION OF NANO-STRUCTURED CHELATING ADSORBENTS FOR THE DIRECT REMOVAL OF MERCURY VAPOR FROM FLUE-GASES.  

E-Print Network [OSTI]

??Coal-Fired utility boilers are currently the largest single-known source of anthropogenic mercury emissions in the United States. In this research, the potential of gas-phase chelating… (more)

ABU-DAABES, MALYUBA ALI

2005-01-01T23:59:59.000Z

157

Separation of particulate from flue gas of fossil fuel combustion and gasification  

DOE Patents [OSTI]

The gas from combustion or gasification of fossil fuel contains flyash and other particulate. The flyash is separated from the gas in a plurality of standleg moving granular-bed filter modules. Each module includes a dipleg through which the bed media flows into the standleg. The bed media forms a first filter bed having an upper mass having a first frusto-conical surface in a frusto-conical member at the entrance to the standleg and a lower mass having a second frusto-conical surface of substantially greater area than the first surface after it passes through the standleg. A second filter media bed may be formed above the first filter media bed. The gas is fed tangentially into the module above the first surface. The flyash is captured on the first frusto-conical surface and within the bed mass. The processed gas flows out through the second frusto-conical surface and then through the second filter bed, if present. The bed media is cleaned of the captured flyash and recirculated to the moving granular bed filter. Alternatively, the bed media may be composed of the ash from the combustion which is pelletized to form agglomerates. The ash flows through the bed only once; it is not recycled.

Yang, Wen-Ching (Murrysville, PA); Newby, Richard A. (Pittsburgh, PA); Lippert, Thomas E. (Murrysville, PA)

1997-01-01T23:59:59.000Z

158

Separation of particulate from flue gas of fossil fuel combustion and gasification  

DOE Patents [OSTI]

The gas from combustion or gasification of fossil fuel contains fly ash and other particulates. The fly ash is separated from the gas in a plurality of standleg moving granular-bed filter modules. Each module includes a dipleg through which the bed media flows into the standleg. The bed media forms a first filter bed having an upper mass having a first frusto-conical surface in a frusto-conical member at the entrance to the standleg and a lower mass having a second frusto-conical surface of substantially greater area than the first surface after it passes through the standleg. A second filter media bed may be formed above the first filter media bed. The gas is fed tangentially into the module above the first surface. The fly ash is captured on the first frusto-conical surface and within the bed mass. The processed gas flows out through the second frusto-conical surface and then through the second filter bed, if present. The bed media is cleaned of the captured fly ash and recirculated to the moving granular bed filter. Alternatively, the bed media may be composed of the ash from the combustion which is pelletized to form agglomerates. The ash flows through the bed only once; it is not recycled. 11 figs.

Yang, W.C.; Newby, R.A.; Lippert, T.E.

1997-08-05T23:59:59.000Z

159

Other States Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

U.S. Energy Information Administration (EIA) Indexed Site

Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Other States Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 513 491 515 539 557 534 541 579 574 585 558 573 1998 578 536 591 581 517 456 486 486 471 477 457 468 1999 466 438 489 495 499 510 547 557 544 555 541 579 2000 587 539 605 587 615 570 653 629 591 627 609 611 2001 658 591 677 690 718 694 692 679 686 697 688 700 2002 639 591 587 621 622 605 654 639 649 650 623 638 2003 689 624 649 676 702 691 733 732 704 734 719 748 2004 741 697 727 692 692 688 718 729 706 723 711 718

160

Process and system for removing impurities from a gas  

DOE Patents [OSTI]

A fluidized reactor system for removing impurities from a gas and an associated process are provided. The system includes a fluidized absorber for contacting a feed gas with a sorbent stream to reduce the impurity content of the feed gas; a fluidized solids regenerator for contacting an impurity loaded sorbent stream with a regeneration gas to reduce the impurity content of the sorbent stream; a first non-mechanical gas seal forming solids transfer device adapted to receive an impurity loaded sorbent stream from the absorber and transport the impurity loaded sorbent stream to the regenerator at a controllable flow rate in response to an aeration gas; and a second non-mechanical gas seal forming solids transfer device adapted to receive a sorbent stream of reduced impurity content from the regenerator and transfer the sorbent stream of reduced impurity content to the absorber without changing the flow rate of the sorbent stream.

Henningsen, Gunnar; Knowlton, Teddy Merrill; Findlay, John George; Schlather, Jerry Neal; Turk, Brian S

2014-04-15T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

Process for off-gas particulate removal and apparatus therefor  

DOE Patents [OSTI]

In the event of a breach in the off-gas line of a melter operation requiring closure of the line, a secondary vessel vent line is provided with a particulate collector utilizing atomization for removal of large particulates from the off-gas. The collector receives the gas containing particulates and directs a portion of the gas through outer and inner annular channels. The collector further receives a fluid, such as water, which is directed through the outer channel together with a second portion of the particulate-laden gas. The outer and inner channels have respective ring-like termination apertures concentrically disposed adjacent one another on the outer edge of the downstream side of the particulate collector. Each of the outer and inner channels curves outwardly away from the collector's centerline in proceeding toward the downstream side of the collector. Gasflow in the outer channel maintains the fluid on the channel's wall in the form of a "wavy film," while the gas stream from the inner channel shears the fluid film as it exits the outer channel in reducing the fluid to small droplets. Droplets formed by the collector capture particulates in the gas stream by one of three mechanisms: impaction, interception or Brownian diffusion in removing the particulates. The particulate-laden droplets are removed from the fluid stream by a vessel vent condenser or mist eliminator.

Carl, Daniel E. (Orchard Park, NY)

1997-01-01T23:59:59.000Z

162

Aminosilane-Grafted Polymer/Silica Hollow Fiber Adsorbents for CO2 Capture from Flue Gas  

Science Journals Connector (OSTI)

In this approach, polymeric hollow fibers similar to those already prepared on commercial scales for membrane gas separations are prepared and loaded with large volumes of solid CO2 adsorbing materials. ... In this regard, the hollow fiber RTSA process is ideally suited for application of typical silica amine adsorbents, as it (i) allows for effective heat integration,(11) (ii) gives fast cycle times (expected to be on the order of 2–4 min),(8) and (iii) minimizes contact of aminosilica-adsorbents with high-temperature steam, which can degrade the adsorbent. ... The moles of CO2 adsorbed were calculated by integration of the area bounded by the CO2 breakthrough front and the He breakthrough front from the initial concentration to the final equilibration concentration. ...

Fateme Rezaei; Ryan P. Lively; Ying Labreche; Grace Chen; Yanfang Fan; William J. Koros; Christopher W. Jones

2013-03-29T23:59:59.000Z

163

An Electrochemically-mediated Gas Separation Process for Carbon Abatement  

E-Print Network [OSTI]

This work describes a promising alternative to conventional thermal processes for absorber/desorber processing of for removal of CO[subscript 2] from flue gas streams at fossil fuel fired power plants. Our electrochemica ...

Stern, Michael C.

164

Feed gas contaminant removal in ion transport membrane systems  

SciTech Connect (OSTI)

An oxygen ion transport membrane process wherein a heated oxygen-containing gas having one or more contaminants is contacted with a reactive solid material to remove the one or more contaminants. The reactive solid material is provided as a deposit on a support. The one or more contaminant compounds in the heated oxygen-containing gas react with the reactive solid material. The contaminant-depleted oxygen-containing gas is contacted with a membrane, and oxygen is transported through the membrane to provide transported oxygen.

Underwood, Richard Paul (Allentown, PA); Makitka, III, Alexander (Hatfield, PA); Carolan, Michael Francis (Allentown, PA)

2012-04-03T23:59:59.000Z

165

Removal of Elemental Mercury from a Gas Stream Facilitated by a Non-Thermal Plasma Device  

SciTech Connect (OSTI)

Mercury generated from anthropogenic sources presents a difficult environmental problem. In comparison to other toxic metals, mercury has a low vaporization temperature. Mercury and mercury compounds are highly toxic, and organic forms such as methyl mercury can be bio-accumulated. Exposure pathways include inhalation and transport to surface waters. Mercury poisoning can result in both acute and chronic effects. Most commonly, chronic exposure to mercury vapor affects the central nervous system and brain, resulting in neurological damage. The CRE technology employs a series of non-thermal, plasma-jet devices to provide a method for elemental mercury removal from a gas phase by targeting relevant chemical reactions. The technology couples the known chemistry of converting elemental mercury to ionic compounds by mercury-chlorine-oxygen reactions with the generation of highly reactive species in a non-thermal, atmospheric, plasma device. The generation of highly reactive metastable species in a non-thermal plasma device is well known. The introduction of plasma using a jet-injection device provides a means to contact highly reactive species with elemental mercury in a manner to overcome the kinetic and mass-transfer limitations encountered by previous researchers. To demonstrate this technology, WRI has constructed a plasma test facility that includes plasma reactors capable of using up to four plasma jets, flow control instrumentation, an integrated control panel to operate the facility, a mercury generation system that employs a temperature controlled oven and permeation tube, combustible and mercury gas analyzers, and a ductless fume hood designed to capture fugitive mercury emissions. Continental Research and Engineering (CR&E) and Western Research Institute (WRI) successfully demonstrated that non-thermal plasma containing oxygen and chlorine-oxygen reagents could completely convert elemental mercury to an ionic form. These results demonstrate potential the application of this technology for removing elemental mercury from flue gas streams generated by utility boilers. On an absolute basis, the quantity of reagent required to accomplish the oxidation was small. For example, complete oxidation of mercury was accomplished using a 1% volume fraction of oxygen in a nitrogen stream. Overall, the tests with mercury validated the most useful aspect of the CR&E technology: Providing a method for elemental mercury removal from a gas phase by employing a specific plasma reagent to either increase reaction kinetics or promote reactions that would not have occurred under normal circumstances.

Charles Mones

2006-12-01T23:59:59.000Z

166

Effect of flue gas impurities on the process of injection and storage of carbon dioxide in depleted gas reservoirs  

E-Print Network [OSTI]

Previous experiments - injecting pure CO2 into carbonate cores - showed that the process is a win-win technology, sequestrating CO2 while recovering a significant amount of hitherto unrecoverable natural gas that could help defray the cost of CO2...

Nogueira de Mago, Marjorie Carolina

2005-11-01T23:59:59.000Z

167

Regenerable Hydrogen Chloride Removal Sorbent and Regenerable Multifunctional Hydrogen Sulfide and Hydrogen Chloride Removal Sorbent for High Temperature Gas Streams  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Hydrogen Chloride and Hydrogen Sulfide Hydrogen Chloride and Hydrogen Sulfide Removal Sorbents for High Temperature Gas Streams Opportunity The Department of Energy's National Energy Technology Laboratory (NETL) is seeking licensing partners interested in implementing United States Patent Number 7,767,000 entitled "Regenerable Hydrogen Chloride Removal Sorbent and Regenerable Multifunctional Hydrogen Sulfide and Hydrogen Chloride Removal Sorbent for High Temperature Gas Streams." Disclosed in this patent is the invention of a unique regenerable sorbent process that can remove contaminants from gas produced by the gasification of fossil fuels. Specifically, the process removes hydrogen chloride by using the regenerable sorbent and simultaneously extracts hydrogen chloride compounds and hydrogen

168

Separation of flue-gas scrubber sludge into marketable products. Second quarterly technical progress report, December 1, 1993--February 28, 1994 (Quarter No. 2)  

SciTech Connect (OSTI)

To reduce their sulfur emissions, many coal-fired electric power plants use wet flue-gas scrubbers. These scrubbers convert sulfur oxides into solid sulfate and sulfite sludge, which must then be disposed of This sludge is a result of reacting limestone with sulfur dioxide to precipitate calcium sulfite and calcium sulfate. It consists of calcium sulfite (CaSO{sub 3}{lg_bullet}0.5H{sub 2}0), gypsum (CaSO{sub 4}{lg_bullet}2H{sub 2}0), and unreacted limestone (CaCO{sub 3}) or lime (Ca(OH){sub 2}), with miscellaneous objectionable impurities such as iron oxides; silica; and magnesium, sodium, and potassium oxides or salts. Currently, the only market for scrubber sludge is for manufacture of gypsum products, such as wallboard and plaster, and for cement. However, the quality of the raw sludge is often not high enough or consistent enough to satisfy manufacturers, and so the material is difficult to sell. This project is developing a process that can produce a high-quality calcium sulfite or gypsum product while keeping process costs low enough that the material produced will be competitive with that from other, more conventional sources. This purification will consist of minimal-reagent froth flotation, using the surface properties of the particles of unreacted limestone to remove them and their associated impurities from the material, leaving a purified gypsum or calcium sulfite product. The separated limestone will be a useful by-product, as it can be recycled to the scrubber, thus boosting the limestone utilization and improving process efficiency. Calcium sulfite will then be oxidized to gypsum, or separated as a salable product in its own right from sludges where it is present in sufficient quantity. The main product of the process will be either gypsum or calcium sulfite, depending on the characteristics of the sludge being processed. These products will be sufficiently pure to be easily marketed, rather that being landfilled.

Kawatra, S.K.; Eisele, T.C.

1994-03-01T23:59:59.000Z

169

Sorbents for the oxidation and removal of mercury  

DOE Patents [OSTI]

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

Olson, Edwin S. (Grand Forks, ND); Holmes, Michael J. (Thompson, ND); Pavlish, John H. (East Grand Forks, MN)

2008-10-14T23:59:59.000Z

170

Sorbents for the oxidation and removal of mercury  

DOE Patents [OSTI]

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

Olson, Edwin S.; Holmes, Michael J.; Pavlish, John Henry

2014-09-02T23:59:59.000Z

171

Method of removing nitrogen monoxide from a nitrogen monoxide-containing gas using a water-soluble iron ion-dithiocarbamate, xanthate or thioxanthate  

DOE Patents [OSTI]

A method of removing nitrogen monoxide from a nitrogen monoxide-containing gas, which method comprises: (a) contacting a nitrogen oxide-containing gas with an aqueous solution of water soluble organic compound-iron ion chelate of the formula: ##STR1## wherein the water-soluble organic compound is selected from compounds of the formula: ##STR2## wherein: R is selected from hydrogen or an organic moiety having at least one polar functional group; Z is selected from oxygen, sulfur, or --N--A wherein N is nitrogen and A is hydrogen or lower alkyl having from one to four carbon atoms; and M is selected from hydrogen, sodium or potassium; and n is 1 or 2, in a contacting zone for a time and at a temperature effective to reduce the nitrogen monoxide. These mixtures are useful to provide an unexpensive method of removing NO from gases, thus reducing atmospheric pollution from flue gases.

Liu, David K. (San Pablo, CA); Chang, Shih-Ger (El Cerrito, CA)

1989-01-01T23:59:59.000Z

172

Removal and determination of trimethylsilanol from the landfill gas  

Science Journals Connector (OSTI)

The removal and determination of trimethylsilanol (TMSOH) in landfill gas has been studied before and after the special E3000-ITC System. The system works according to principle of temperature swing. The performance of TMSOH and humidity removal was 20% and more than 90%, respectively. The six of active carbons and impinger method were tested on the full-scale landfill in Poland for TMSOH and siloxanes determination. The extraction method and absorption in acetone were used. The concentration of TMSOH and siloxanes were found in range from 23.6 to 29.2 mg/m3 and from 18.0 to 38.9 mg/m3, respectively. The content of TMSOH in biogas originating from landfill was 41% out of all siloxanes. Moreover, the used system is alternative to other existing technique of landfill gas purification.

Grzegorz Piechota; Manfred Hagmann; Roman Buczkowski

2012-01-01T23:59:59.000Z

173

Adsorption and desorption of sulfur dioxide on novel adsorbents for flue gas desulfurization. Final report, September 1, 1994--February 29, 1996  

SciTech Connect (OSTI)

A sol-gel granulation method was developed to prepare spherical {gamma}-alumina granular supports and supported CuO granular sorbents for flue gas desulfurization. The prepared {gamma}-alumina supported CuO sorbents exhibit desirable pore structure and excellent mechanical properties. The sorbents contain higher loading (30-40 wt. %) of CuO dispersed in the monolayer or sub-monolayer form, giving rise to a larger SO{sub 2} sorption capacity ({gt}20 wt.%) and a faster sorption rate as compared to similar sorbents reported in the literature. With these excellent sulfation and mechanical properties, the sol-gel derived {gamma}-alumina supported CuO granular sorbents offer great potential for use in the dry, regenerative flue gas desulfurization process. Research efforts were also made to prepare DAY zeolite supported sorbents with various CuO contents by the microwave and conventional thermal dispersion methods at different conditions. Monolayer or sub-monolayer coating of Cu(NO{sub 3})sub 2 or CuO was achieved on several DAY supported sorbents by the microwave heating method but not by the conventional thermal dispersion method. The DAY zeolite supported CuO sorbents prepared by the microwave heating method can adsorb up to 15 wt.% of SO{sub 2}. The results obtained have demonstrated the feasibility of effective preparation of zeolite supported CuO sorbents by the microwave heating method.

Lin, Y.S.; Deng, S.G.

1996-08-05T23:59:59.000Z

174

Low-quality natural gas sulfur removal/recovery  

SciTech Connect (OSTI)

A significant fraction of U.S. natural gas reserves are subquality due to the presence of acid gases and nitrogen; 13% of existing reserves (19 trillion cubic feed) may be contaminated with hydrogen sulfide. For natural gas to be useful as fuel and feedstock, this hydrogen sulfide has to be removed to the pipeline specification of 4 ppm. The technology used to achieve these specifications has been amine, or similar chemical or physical solvent, absorption. Although mature and widely used in the gas industry, absorption processes are capital and energy-intensive and require constant supervision for proper operation. This makes these processes unsuitable for treating gas at low throughput, in remote locations, or with a high concentration of acid gases. The U.S. Department of Energy, recognizes that exploitation of smaller, more sub-quality resources will be necessary to meet demand as the large gas fields in the U.S. are depleted. In response to this need, Membrane Technology and Research, Inc. (MTR) has developed membranes and a membrane process for removing hydrogen sulfide from natural gas. During this project, high-performance polymeric thin-film composite membranes were brought from the research stage to field testing. The membranes have hydrogen sulfide/methane selectivities in the range 35 to 60, depending on the feed conditions, and have been scaled up to commercial-scale production. A large number of spiral-wound modules were manufactured, tested and optimized during this project, which culminated in a field test at a Shell facility in East Texas. The short field test showed that membrane module performance on an actual natural gas stream was close to that observed in the laboratory tests with cleaner streams. An extensive technical and economic analysis was performed to determine the best applications for the membrane process. Two areas were identified: the low-flow-rate, high-hydrogen-sulfide-content region and the high-flow-rate, high-hydrogen-sulfide-content region. In both regions the MTR membrane process will be combined with another process to provide the necessary hydrogen sulfide removal from the natural gas. In the first region the membrane process will be combined with the SulfaTreat fixed-bed absorption process, and in the second region the membrane process will be combined with a conventional absorption process. Economic analyses indicate that these hybrid processes provide 20-40% cost savings over stand-alone absorption technologies.

K. Amo; R.W. Baker; V.D. Helm; T. Hofmann; K.A. Lokhandwala; I. Pinnau; M.B. Ringer; T.T. Su; L. Toy; J.G. Wijmans

1998-01-29T23:59:59.000Z

175

Illinois Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0

176

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA

177

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

U.S. Energy Information Administration (EIA) Indexed Site

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA

178

Method for the removal of elemental mercury from a gas stream  

DOE Patents [OSTI]

A method is provided to remove elemental mercury from a gas stream by reacting the gas stream with an oxidizing solution to convert the elemental mercury to soluble mercury compounds. Other constituents are also oxidized. The gas stream is then passed through a wet scrubber to remove the mercuric compounds and oxidized constituents.

Mendelsohn, Marshall H. (Downers Grove, IL); Huang, Hann-Sheng (Darien, IL)

1999-01-01T23:59:59.000Z

179

Method for high temperature mercury capture from gas streams  

DOE Patents [OSTI]

A process to facilitate mercury extraction from high temperature flue/fuel gas via the use of metal sorbents which capture mercury at ambient and high temperatures. The spent sorbents can be regenerated after exposure to mercury. The metal sorbents can be used as pure metals (or combinations of metals) or dispersed on an inert support to increase surface area per gram of metal sorbent. Iridium and ruthenium are effective for mercury removal from flue and smelter gases. Palladium and platinum are effective for mercury removal from fuel gas (syngas). An iridium-platinum alloy is suitable for metal capture in many industrial effluent gas streams including highly corrosive gas streams.

Granite, E.J.; Pennline, H.W.

2006-04-25T23:59:59.000Z

180

Fuel saving, carbon dioxide emission avoidance, and syngas production by tri-reforming of flue gases from coal- and gas-fired power stations, and by the carbothermic reduction of iron oxide  

Science Journals Connector (OSTI)

Flue gases from coal, gas, or oil-fired power stations, as well as from several heavy industries, such as the production of iron, lime and cement, are major anthropogenic sources of global CO2 emissions. The newly proposed process for syngas production based on the tri-reforming of such flue gases with natural gas could be an important route for CO2 emission avoidance. In addition, by combining the carbothermic reduction of iron oxide with the partial oxidation of the carbon source, an overall thermoneutral process can be designed for the co-production of iron and syngas rich in CO. Water-gas shift (WGS) of CO to H2 enables the production of useful syngas. The reaction process heat, or the conditions for thermoneutrality, are derived by thermochemical equilibrium calculations. The thermodynamic constraints are determined for the production of syngas suitable for methanol, hydrogen, or ammonia synthesis. The environmental and economic consequences are assessed for large-scale commercial production of these chemical commodities. Preliminary evaluations with natural gas, coke, or coal as carbon source indicate that such combined processes should be economically competitive, as well as promising significant fuel saving and CO2 emission avoidance. The production of ammonia in the above processes seems particularly attractive, as it consumes the nitrogen in the flue gases.

M. Halmann; A. Steinfeld

2006-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

Steam Reactivation and Separation of Limestone Sorbents for High Temperature Post-combustion CO2 Capture from Flue Gas.  

E-Print Network [OSTI]

?? Increasing global population and demand for energy has raised concerns of excessive anthropogenic greenhouse gas emissions from consumption of fossil fuels. Coal, in particular,… (more)

Wang, Alan Yao

2012-01-01T23:59:59.000Z

182

Apparatus and method for removing mercury vapor from a gas stream  

DOE Patents [OSTI]

A metallic filter effectively removes mercury vapor from gas streams. The filter captures the mercury which then can be released and collected as product. The metallic filter is a copper mesh sponge plated with a six micrometer thickness of gold. The filter removes up to 90% of mercury vapor from a mercury contaminated gas stream.

Ganesan, Kumar (Butte, MT)

2008-01-01T23:59:59.000Z

183

Method for combined removal of mercury and nitrogen oxides from off-gas streams  

DOE Patents [OSTI]

A method for removing elemental Hg and nitric oxide simultaneously from a gas stream is provided whereby the gas stream is reacted with gaseous chlorinated compound to convert the elemental mercury to soluble mercury compounds and the nitric oxide to nitrogen dioxide. The method works to remove either mercury or nitrogen oxide in the absence or presence of each other.

Mendelsohn, Marshall H. (Downers Grove, IL); Livengood, C. David (Lockport, IL)

2006-10-10T23:59:59.000Z

184

Simulation study on lignite-fired power system integrated with flue gas drying and waste heat recovery – Performances under variable power loads coupled with off-design parameters  

Science Journals Connector (OSTI)

Abstract Lignite is a kind of low rank coal with high moisture content and low net heating value, which is mainly used for electric power generation. However, the thermal efficiency of power plants firing lignite directly is very low. Pre-drying is a proactive option, dehydrating raw lignite to raise its heating value, to improve the power plant thermal efficiency. A pre-dried lignite-fired power system integrated with boiler flue gas drying and waste heat recovery was proposed in this paper. The plant thermal efficiency could be improved by 1.51% at benchmark condition due to pre-drying and waste heat recovery. The main system performances under variable power loads were simulated and analyzed. Simulation results show that the improvement of plant thermal efficiency reduced to 1.36% at 50% full load. Moreover, the influences of drying system off-design parameters were simulated coupled with power loads. The variation tendencies of main system parameters were obtained. The influence of pre-drying degree (including moisture content of pre-dried lignite and raw lignite) on the plant thermal efficiency diminishes gradually with the decreasing power load. The dryer thermal efficiency and dryer exhaust temperature are also main factors and the influences on system parameters have been quantitatively analyzed.

Xiaoqu Han; Ming Liu; Jinshi Wang; Junjie Yan; Jiping Liu; Feng Xiao

2014-01-01T23:59:59.000Z

185

FASTCHEM/trademark/ (Fly Ash and Flue Gas Desulfurization Sludge Transport and Geochemistry) package: Volume 2, User's guide to the EFLOW groundwater flow code  

SciTech Connect (OSTI)

This report documents a two-dimensional finite element code, EFLOW, developed to simulate water flow in fully or variably saturated porous media. This code is one component in the FASTCHEM/trademark/ (Fly Ash and Flue Gas Desulfurization Sludge Transport and Geochemistry) package. The formulation of the governing equations and the numerical procedures used in the code are presented. The flow equation is approximated using the Galerkin finite element method. For variably saturated flow problems, nonlinearities caused by unsaturated soil properties, atmospheric boundary conditions (e.g., infiltration, evaporation and seepage faces), and water uptake by plant roots are treated using Picard or Newton-Raphson methods. For fully saturated unconfined flow problems, the governing equations are formulated in an areal plane, and nonlinear water-table boundary conditions are treated using the Picard method. Several test problems are presented to verify the code and demonstrate its utility. These problems range from simple one-dimensional to complex two-dimensional and axisymmetric problems. 24 refs., 39 figs., 27 tabs.

Not Available

1988-09-01T23:59:59.000Z

186

Selection of an acid-gas removal process for an LNG plant  

SciTech Connect (OSTI)

Acid gas contaminants, such as, CO{sub 2}, H{sub 2}S and mercaptans, must be removed to a very low level from a feed natural gas before it is liquefied. CO{sub 2} is typically removed to a level of about 100 ppm to prevent freezing during LNG processing. Sulfur compounds are removed to levels required by the eventual consumer of the gas. Acid-gas removal processes can be broadly classified as: solvent-based, adsorption, cryogenic or physical separation. The advantages and disadvantages of these processes will be discussed along with design and operating considerations. This paper will also discuss the important considerations affecting the choice of the best acid-gas removal process for LNG plants. Some of these considerations are: the remoteness of the LNG plant from the resource; the cost of the feed gas and the economics of minimizing capital expenditures; the ultimate disposition of the acid gas; potential for energy integration; and the composition, including LPG and conditions of the feed gas. The example of the selection of the acid-gas removal process for an LNG plant.

Stone, J.B.; Jones, G.N. [Exxon Production Research, Houston, TX (United States); Denton, R.D. [Exxon Production Malaysia, Inc., Kuala Lumpur (Malaysia)

1996-12-31T23:59:59.000Z

187

Method for removing metal vapor from gas streams  

DOE Patents [OSTI]

A process for cleaning an inert gas contaminated with a metallic vapor, such as cadmium, involves withdrawing gas containing the metallic contaminant from a gas atmosphere of high purity argon; passing the gas containing the metallic contaminant to a mass transfer unit having a plurality of hot gas channels separated by a plurality of coolant gas channels; cooling the contaminated gas as it flows upward through the mass transfer unit to cause contaminated gas vapor to condense on the gas channel walls; regenerating the gas channels of the mass transfer unit; and, returning the cleaned gas to the gas atmosphere of high purity argon. The condensing of the contaminant-containing vapor occurs while suppressing contaminant particulate formation, and is promoted by providing a sufficient amount of surface area in the mass transfer unit to cause the vapor to condense and relieve supersaturation buildup such that contaminant particulates are not formed. Condensation of the contaminant is prevented on supply and return lines in which the contaminant containing gas is withdrawn and returned from and to the electrorefiner and mass transfer unit by heating and insulating the supply and return lines.

Ahluwalia, R. K. (6440 Hillcrest Dr., Burr Ridge, IL 60521); Im, K. H. (925 Lehigh Cir., Naperville, IL 60565)

1996-01-01T23:59:59.000Z

188

CO2 Separation from Low-Temperature Flue Gases  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

partners interested in implementing United States Patent Number 7,842,126 entitled "Co 2 Separation from Low-Temperature Flue Gases." Disclosed in this patent are novel methods for processing carbon dioxide (CO 2 ) from combustion gas streams. Researchers at NETL are focused on the development of novel sorbent systems that can effectively remove CO 2 and other gases in an economically feasible manner with limited impact on energy production cost. The current invention will help in reducing greenhouse gas emissions by using an improved, regenerable aqueous amine and soluble potassium carbonate sorbent system. This novel solvent system may be capable of achieving CO 2 capture from larger emission streams at lower overall cost. Overview Sequestration of CO

189

Chapter 26 - The Oxyfuel Baseline: Revamping Heaters and Boilers to Oxyfiring by Cryogenic Air Separation and Flue Gas Recycle  

Science Journals Connector (OSTI)

This feasibility study involves the potential application of oxyfuel technology on a refinery-wide basis at the BP Grangemouth unit in Scotland. A total of seven boilers and 13 process heaters of various types, burning a mixture of refinery fuel gas and fuel oil resulting in the production of approximately 2.0 million tonnes per annum of CO2, form the basis of this study.

Rodney Allam; Vince White; Neil Ivens; Mark Simmonds

2005-01-01T23:59:59.000Z

190

Improved high efficiency third stage separator cyclones for separation of fines from fluid catalytic cracking flue gas  

SciTech Connect (OSTI)

Stairmand type small diameter (0.254 m) multicyclones were cold flow tested for fluid catalytic cracking third stage separator application. The gas discharge from the cyclone dust outlet into the common collection hopper was found to far exceed the hopper bleed rate (underflow). The excess gas reentrained dust from the hopper back into cyclones, which lowered collection efficiencies. Vortex {open_quotes}stabilization{close_quotes} using apex cones was unsuccessful whereas a Mobil proprietary cyclone modification was successful in minimizing excess gas discharge and dust reentrainment at the cyclone-hopper boundary. In tests at 700 {degrees}C, the modified cyclones captured all particles above 4 {mu}m. Mobil-Kellogg incorporated the modified cyclones in a new third stage separator design which is targeted for achieving lowest opacity and <50 mg/Nm{sup 3} emissions at the stack. The first such unit will be commercialized in Mobil`s newest catalytic cracker (M.W. Kellogg design) under construction in Altona, Australia in late 1996. 5 refs., 4 figs., 2 tabs.

Chitnis, G.K.; Schatz, K.W. [Mobil Technology Co., Paulsboro, NJ (United States); Bussey, B.K. [M.W. Kellogg Co., Houston, TX (United States)

1996-12-31T23:59:59.000Z

191

Feed gas contaminant removal in ion transport membrane systems  

DOE Patents [OSTI]

Method for gas purification comprising (a) obtaining a feed gas stream containing one or more contaminants selected from the group consisting of volatile metal oxy-hydroxides, volatile metal oxides, and volatile silicon hydroxide; (b) contacting the feed gas stream with a reactive solid material in a guard bed and reacting at least a portion of the contaminants with the reactive solid material to form a solid reaction product in the guard bed; and (c) withdrawing from the guard bed a purified gas stream.

Carolan, Michael Francis (Allentown, PA); Miller, Christopher Francis (Macungie, PA)

2008-09-16T23:59:59.000Z

192

Organoclay Sorbent for Removal of Carbon Dioxide from Gas Streams at Low Temperatures  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Organoclay Sorbent for Removal of Carbon Dioxide from Gas Organoclay Sorbent for Removal of Carbon Dioxide from Gas Streams at Low Temperatures Contact NETL Technology Transfer Group techtransfer@netl.doe.gov October 2012 Significance * Energy mixing is maximized * Mobilizing of the particulates is complete * No "dead zones" exist * Packing of material is minimized * Eroding effects are significantly reduced Applications * Mixing nuclear waste at Hanford * Any similar industrial process involving heavy solids in a carrier fluid Opportunity Research is currently active on the patent-pending technology "Organoclay Sorbent for Removal of Carbon Dioxide from

193

Anode shroud for off-gas capture and removal from electrolytic oxide reduction system  

DOE Patents [OSTI]

An electrolytic oxide reduction system according to a non-limiting embodiment of the present invention may include a plurality of anode assemblies and an anode shroud for each of the anode assemblies. The anode shroud may be used to dilute, cool, and/or remove off-gas from the electrolytic oxide reduction system. The anode shroud may include a body portion having a tapered upper section that includes an apex. The body portion may have an inner wall that defines an off-gas collection cavity. A chimney structure may extend from the apex of the upper section and be connected to the off-gas collection cavity of the body portion. The chimney structure may include an inner tube within an outer tube. Accordingly, a sweep gas/cooling gas may be supplied down the annular space between the inner and outer tubes, while the off-gas may be removed through an exit path defined by the inner tube.

Bailey, James L.; Barnes, Laurel A.; Wiedmeyer, Stanley G.; Williamson, Mark A.; Willit, James L.

2014-07-08T23:59:59.000Z

194

Removing a small quantity of THT from gas storage groundwater through air stripping and gas-phase carbon adsorption  

SciTech Connect (OSTI)

This paper deals with the response to a case of contaminated groundwater located in France. The natural gas is stored during summer in porous underground rocks. When energy requirements increase (particularly in winter), gas is drawn off, but water is also pumped during this operation. The water has a strong characteristic odour of the TetraHydroThiophene (THT), which has been used by Gaz de France as an additive in order to detect gas leakages because of its strong odour. Unfortunately, the presence of THT in medium other than natural gas can be responsible for safety problems. Gas stripping combined with adsorption on granular activated carbon was chosen to obtain removal of THT from the groundwater. The gas to water ratio for stripping column is higher than usual and the gas used for stripping was recycled in order to prevent air pollution. Carbon consumption is approximately 3 tons a year. 8 refs., 5 figs., 2 tabs.

Girod, J.F.; Leclerc, J.P.; Muhr, H. [CNRS, Nancy (France)] [and others

1996-12-31T23:59:59.000Z

195

Apparatus for removal of particulate matter from gas streams  

DOE Patents [OSTI]

An apparatus for the removal of particulate matter from the gaseous product stream of an entrained flow coal gasifier which apparatus includes an initial screen, an intermediate screen which is aligned with the direction of flow of the gaseous product stream and a final screen transversely disposed to the flow of gaseous product and which apparatus is capable of withstanding at least a pressure differential of about 10 psi (68.95 kPa) or greater at the temperatures of the gaseous product stream.

Smith, Peyton L. (Baton Rouge, LA); Morse, John C. (Baton Rouge, LA)

2000-01-01T23:59:59.000Z

196

Solid Sorbents for Removal of Carbon Dioxide from Gas Streams at Low Temperatures  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Sorbents for Removal of Carbon Dioxide from Sorbents for Removal of Carbon Dioxide from Gas Streams at Low Temperatures Opportunity The Department of Energy's National Energy Technology Laboratory is seeking licensing partners interested in implementing United States Patent Number 6,908,497 entitled "Solid Sorbents for Removal of Carbon Dioxide from Gas Streams at Low Temperatures." Disclosed in this patent is a new low-cost carbon dioxide (CO 2 ) sorbent that can be used in large-scale gas-solid processes. Researchers have developed a new method to prepare these sorbents by treating substrates with an amine and/or an ether in a way that either one comprises at least 50 weight percent of the sorbent. The sorbent captures compounds contained in gaseous fluids through chemisorptions and/or

197

HYBRID SELECTIVE NON-CATALYTIC REDUCTION (SNCR)/SELECTIVE CATALYTIC REDUCTION (SCR) DEMONSTRATION FOR THE REMOVAL OF NOx FROM BOILER FLUE GASES  

SciTech Connect (OSTI)

The U. S. Department of Energy (DOE), Electric Power Research Institute (EPRI), Pennsylvania Electric Energy Research Council, (PEERC), New York State Electric and Gas and GPU Generation, Inc. jointly funded a demonstration to determine the capabilities for Hybrid SNCR/SCR (Selective Non-Catalytic Reduction/Selective Catalytic Reduction) technology. The demonstration site was GPU Generation's Seward Unit No.5 (147MW) located in Seward Pennsylvania. The demonstration began in October of 1997 and ended in December 1998. DOE funding was provided through Grant No. DE-FG22-96PC96256 with T. J. Feeley as the Project Manager. EPRI funding was provided through agreements TC4599-001-26999 and TC4599-002-26999 with E. Hughes as the Project Manager. This project demonstrated the operation of the Hybrid SNCR/SCR NO{sub x} control process on a full-scale coal fired utility boiler. The hybrid technology was expected to provide a cost-effective method of reducing NO{sub x} while balancing capital and operation costs. An existing urea based SNCR system was modified with an expanded-duct catalyst to provide increased NO{sub x} reduction efficiency from the SNCR while producing increased ammonia slip levels to the catalyst. The catalyst was sized to reduce the ammonia slip to the air heaters to less than 2 ppm while providing equivalent NO{sub x} reductions. The project goals were to demonstrate hybrid technology is capable of achieving at least a 55% reduction in NO{sub x} emissions while maintaining less than 2ppm ammonia slip to the air heaters, maintain flyash marketability, verify the cost benefit and applicability of Hybrid post combustion technology, and reduce forced outages due to ammonium bisulfate (ABS) fouling of the air heaters. Early system limitations, due to gas temperature stratification, restricted the Hybrid NO{sub x} reduction capabilities to 48% with an ammonia slip of 6.1 mg/Nm{sup 3} (8 ppm) at the catalyst inlet. After resolving the stratification problem, the catalyst did not have sufficient activity in order to continue the planned test program. Arsenic poisoning was found to be the cause of premature catalyst deactivation.

Jerry B. Urbas

1999-05-01T23:59:59.000Z

198

Removing sulphur oxides from a fluid stream  

DOE Patents [OSTI]

A process for removing sulphur oxides from a fluid stream, such as flue gas, comprising: providing a non-aqueous absorption liquid containing at least one hydrophobic amine, the liquid being incompletely miscible with water; treating the fluid stream in an absorption zone with the non-aqueous absorption liquid to transfer at least part of the sulphur oxides into the non-aqueous absorption liquid and to form a sulphur oxide-hydrophobic amine-complex; causing the non-aqueous absorption liquid to be in liquid-liquid contact with an aqueous liquid whereby at least part of the sulphur oxide-hydrophobic amine-complex is hydrolyzed to release the hydrophobic amine and sulphurous hydrolysis products, and at least part of the sulphurous hydrolysis products is transferred into the aqueous liquid; separating the aqueous liquid from the non-aqueous absorption liquid. The process mitigates absorbent degradation problems caused by sulphur dioxide and oxygen in flue gas.

Katz, Torsten; Riemann, Christian; Bartling, Karsten; Rigby, Sean Taylor; Coleman, Luke James Ivor; Lail, Marty Alan

2014-04-08T23:59:59.000Z

199

Carbon dioxide removal and capture for landfill gas up-grading  

Science Journals Connector (OSTI)

Within the frame of an EC financially supported project - LIFE05 ENV/IT/000874 GHERL (Greenhouse Effect Reduction from Landfill)–a pilot plant was set up in order to demonstrate the feasibility of applying chemical absorption to remove carbon dioxide from landfill gas. After proper upgrading - basically removal of carbon dioxide, hydrogen sulphide, ammonia and other trace gas compound–the gas might be fed into the distribution grid for natural gas or used as vehicle fuel, replacing a fossil fuel thus saving natural resources and carbon dioxide emissions. Several experiences in Europe have been carried out concerning the landfill gas - and biogas from anaerobic digestion - quality up-grading through CO2 removal, but in all of them carbon dioxide was vented to the atmosphere after separation, without any direct benefit in terms of greenhouse gases reduction. With respect to those previous experiences, in this work the attention was focused on CO2 removal from landfill gas with an effective capture process, capable of removing carbon dioxide from atmosphere, through a globally carbon negative process. In particular, processes capable of producing final solid products were investigated, with the aim of obtaining as output solid compounds which can be either used in the chemical industry or disposed off. The adopted absorption process is based on using aqueous solutions of potassium hydroxide, with the final aim of producing potassium carbonate. Potassium carbonate is a product which has several applications in the chemical industry if obtained with adequate quality. It can be sold as a pulverised solid, or in aqueous solution. Several tests were carried out at the pilot plant, which was located at a landfill site, in order to feed it with a fraction of the on-site collected landfill gas. The results of the experimental campaign are reported, explained and commented in the paper. Also a discussion on economic issues is presented.

Lidia Lombardia; Andrea Corti; Ennio Carnevale; Renato Baciocchi; Daniela Zingaretti

2011-01-01T23:59:59.000Z

200

Mercury removal in utility wet scrubber using a chelating agent  

DOE Patents [OSTI]

A method for capturing and reducing the mercury content of an industrial flue gas such as that produced in the combustion of a fossil fuel or solid waste adds a chelating agent, such as ethylenediaminetetraacetic acid (EDTA) or other similar compounds like HEDTA, DTPA and/or NTA, to the flue gas being scrubbed in a wet scrubber used in the industrial process. The chelating agent prevents the reduction of oxidized mercury to elemental mercury, thereby increasing the mercury removal efficiency of the wet scrubber. Exemplary tests on inlet and outlet mercury concentration in an industrial flue gas were performed without and with EDTA addition. Without EDTA, mercury removal totaled 42%. With EDTA, mercury removal increased to 71%. The invention may be readily adapted to known wet scrubber systems and it specifically provides for the removal of unwanted mercury both by supplying S.sup.2- ions to convert Hg.sup.2+ ions into mercuric sulfide (HgS) and by supplying a chelating agent to sequester other ions, including but not limited to Fe.sup.2+ ions, which could otherwise induce the unwanted reduction of Hg.sup.2+ to the form, Hg.sup.0.

Amrhein, Gerald T. (Louisville, OH)

2001-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Gas-Liquid Contact Area of Random and Structured Packing Ian David Wilson, B.S.  

E-Print Network [OSTI]

of the gas or to avoid catalyst poisoning. It is becoming apparent that CO2 emissions may also play a mayor the flue gas and the liquid solvent. The gas exits from the top with a low concentration of CO2 while 1.1 CO2 removal by absorption/stripping Absorber Stripper Sweet Gas CO2 + H2O Sour Gas Rich Amine

Rochelle, Gary T.

202

Removing a sheet from the surface of a melt using gas jets  

DOE Patents [OSTI]

In one embodiment, a sheet production apparatus comprises a vessel configured to hold a melt of a material. A cooling plate is disposed proximate the melt and is configured to form a sheet of the material on the melt. A first gas jet is configured to direct a gas toward an edge of the vessel. A sheet of a material is translated horizontally on a surface of the melt and the sheet is removed from the melt. The first gas jet may be directed at the meniscus and may stabilize this meniscus or increase local pressure within the meniscus.

Kellerman, Peter L; Thronson, Gregory D; Sun, Dawei

2014-04-01T23:59:59.000Z

203

NETL: News Release - Innovative Mercury Removal Technique Shows Early  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

August 5, 2003 August 5, 2003 Innovative Mercury Removal Technique Shows Early Promise Photochemical Process Developed in Federal Lab Removes Mercury from Flue Gas - NETL scientist Evan Granite prepares a lab test of the UV mercury removal process. - NETL scientist Evan Granite prepares for a lab test of the UV mercury removal process. MORGANTOWN, WV - A promising technology to remove mercury from coal-fired power plants -- dubbed the "GP-254 Process" -- has been developed and is currently being tested at the Department of Energy's National Energy Technology Laboratory (NETL). Newly patented, the GP-254 Process enhances mercury removal using ultraviolet light to induce various components of power plant stack gas to react with the mercury, and changes the

204

Methods and compositions for removing carbon dioxide from a gaseous mixture  

DOE Patents [OSTI]

Provided is a method for adsorbing or separating carbon dioxide from a mixture of gases by passing the gas mixture through a porous three-dimensional polymeric coordination compound having a plurality of layers of two-dimensional arrays of repeating structural units, which results in a lower carbon dioxide content in the gas mixture. Thus, this invention provides useful compositions and methods for removal of greenhouse gases, in particular CO.sub.2, from industrial flue gases or from the atmosphere.

Li, Jing; Wu, Haohan

2014-06-24T23:59:59.000Z

205

Superstructure Optimization: Reaction Yield Dependent CO2 Removal from OCM Product Gas  

Science Journals Connector (OSTI)

Abstract The oxidative coupling of methane presents an alternative for the production of ethene as opposed to the standard steam cracking of crude oil. A drawback of the reaction is the byproduct creation of CO2. Due to economic reasons, CO2 needs to be removed from the product gas efficiently, while keeping the ethene loss below 5%. Therefore, an overall assessment of the reaction and gas purification section of an OCM process is required. In the past, experiments have shown that a combination of various gas separation membranes with an absorption-desorption process leads to efficient hybrid separation processes. In this contribution, superstructure optimization of the separation section is performed combining various gas separation membranes (in type and number) with an absorption-desorption process and using different input values of CO2 and ethene concentrations leading to a significant energy reduction compared to standard absorption processes.

Christian Bock; Erik Esche; David Müller; Günter Wozny

2014-01-01T23:59:59.000Z

206

,"Ohio Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

U.S. Energy Information Administration (EIA) Indexed Site

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030oh2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030oh2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:25 AM" "Back to Contents","Data 1: Ohio Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030OH2" "Date","Ohio Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 33253,0 33284,0 33312,0

207

,"Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

U.S. Energy Information Administration (EIA) Indexed Site

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030tn2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030tn2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:27 AM" "Back to Contents","Data 1: Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030TN2" "Date","Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 33253,0 33284,0

208

,"Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

U.S. Energy Information Administration (EIA) Indexed Site

Annual",2010 Annual",2010 ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030tn2a.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030tn2a.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:27 AM" "Back to Contents","Data 1: Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030TN2" "Date","Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 35611,0 35976,0 37802,0 38898,0

209

,"Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

U.S. Energy Information Administration (EIA) Indexed Site

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030va2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030va2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:29 AM" "Back to Contents","Data 1: Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030VA2" "Date","Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 33253,0 33284,0

210

,"Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

U.S. Energy Information Administration (EIA) Indexed Site

Annual",2010 Annual",2010 ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030pa2a.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030pa2a.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:26 AM" "Back to Contents","Data 1: Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030PA2" "Date","Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 35611,0 35976,0 37802,0

211

,"South Dakota Natural Gas Nonhydrocarbon Gases Removed (MMcf)"  

U.S. Energy Information Administration (EIA) Indexed Site

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030sd2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030sd2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:26 AM" "Back to Contents","Data 1: South Dakota Natural Gas Nonhydrocarbon Gases Removed (MMcf)" "Sourcekey","N9030SD2" "Date","South Dakota Natural Gas Nonhydrocarbon Gases Removed (MMcf)" 33253,0 33284,0 33312,0 33343,0 33373,0

212

,"Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

U.S. Energy Information Administration (EIA) Indexed Site

Annual",2010 Annual",2010 ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030va2a.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030va2a.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:29 AM" "Back to Contents","Data 1: Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030VA2" "Date","Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 35611,0 35976,0 37802,0 38898,0

213

,"Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

U.S. Energy Information Administration (EIA) Indexed Site

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030pa2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030pa2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:26 AM" "Back to Contents","Data 1: Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030PA2" "Date","Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 33253,0

214

Evaluation of a Combined Cyclone and Gas Filtration System for Particulate Removal in the Gasification Process  

SciTech Connect (OSTI)

The Wabash gasification facility, owned and operated by sgSolutions LLC, is one of the largest single train solid fuel gasification facilities in the world capable of transforming 2,000 tons per day of petroleum coke or 2,600 tons per day of bituminous coal into synthetic gas for electrical power generation. The Wabash plant utilizes Phillips66 proprietary E-Gas (TM) Gasification Process to convert solid fuels such as petroleum coke or coal into synthetic gas that is fed to a combined cycle combustion turbine power generation facility. During plant startup in 1995, reliability issues were realized in the gas filtration portion of the gasification process. To address these issues, a slipstream test unit was constructed at the Wabash facility to test various filter designs, materials and process conditions for potential reliability improvement. The char filtration slipstream unit provided a way of testing new materials, maintenance procedures, and process changes without the risk of stopping commercial production in the facility. It also greatly reduced maintenance expenditures associated with full scale testing in the commercial plant. This char filtration slipstream unit was installed with assistance from the United States Department of Energy (built under DOE Contract No. DE-FC26-97FT34158) and began initial testing in November of 1997. It has proven to be extremely beneficial in the advancement of the E-Gas (TM) char removal technology by accurately predicting filter behavior and potential failure mechanisms that would occur in the commercial process. After completing four (4) years of testing various filter types and configurations on numerous gasification feed stocks, a decision was made to investigate the economic and reliability effects of using a particulate removal gas cyclone upstream of the current gas filtration unit. A paper study had indicated that there was a real potential to lower both installed capital and operating costs by implementing a char cyclonefiltration hybrid unit in the E-Gas (TM) gasification process. These reductions would help to keep the E-Gas (TM) technology competitive among other coal-fired power generation technologies. The Wabash combined cyclone and gas filtration slipstream test program was developed to provide design information, equipment specification and process control parameters of a hybrid cyclone and candle filter particulate removal system in the E-Gas (TM) gasification process that would provide the optimum performance and reliability for future commercial use. The test program objectives were as follows: 1. Evaluate the use of various cyclone materials of construction; 2. Establish the optimal cyclone efficiency that provides stable long term gas filter operation; 3. Determine the particle size distribution of the char separated by both the cyclone and candle filters. This will provide insight into cyclone efficiency and potential future plant design; 4. Determine the optimum filter media size requirements for the cyclone-filtration hybrid unit; 5. Determine the appropriate char transfer rates for both the cyclone and filtration portions of the hybrid unit; 6. Develop operating procedures for the cyclone-filtration hybrid unit; and, 7. Compare the installed capital cost of a scaled-up commercial cyclone-filtration hybrid unit to the current gas filtration design without a cyclone unit, such as currently exists at the Wabash facility.

Rizzo, Jeffrey J. [Phillips66 Company, West Terre Haute, IN (United States)

2010-04-30T23:59:59.000Z

215

MULTIPLE POLLUTANT REMOVAL USING THE CONDENSING HEAT EXCHANGER  

SciTech Connect (OSTI)

The Integrated Flue Gas Treatment (IFGT) system is a new concept whereby a Teflon ® covered condensing heat exchanger is adapted to remove certain flue gas constituents, both particulate and gaseous, while recovering low level heat. The pollutant removal performance and durability of this device is the subject of a USDOE sponsored program to develop this technology. The program was conducted under contract to the United States Department of Energy?s Fossil Energy Technology Center (DOE-FETC) and was supported by the Ohio Coal Development Office (OCDO) within the Ohio Department of Development, the Electric Power Research Institute?s Environmental Control Technology Center (EPRI-ECTC) and Babcock and Wilcox - a McDermott Company (B&W). This report covers the results of the first phase of this program. This Phase I project has been a two year effort. Phase I includes two experimental tasks. One task dealt principally with the pollutant removal capabilities of the IFGT at a scale of about 1.2MWt. The other task studied the durability of the Teflon ® covering to withstand the rigors of abrasive wear by fly ash emitted as a result of coal combustion. The pollutant removal characteristics of the IFGT system were measured over a wide range of operating conditions. The coals tested included high, medium and low-sulfur coals. The flue gas pollutants studied included ammonia, hydrogen chloride, hydrogen fluoride, particulate, sulfur dioxide, gas phase and particle phase mercury and gas phase and particle phase trace elements. The particulate removal efficiency and size distribution was investigated. These test results demonstrated that the IFGT system is an effective device for both acid gas absorption and fine particulate collection. Although soda ash was shown to be the most effective reagent for acid gas absorption, comparative cost analyses suggested that magnesium enhanced lime was the most promising avenue for future study. The durability of the Teflon ® covered heat exchanger tubes was studied on a pilot-scale single- stage condensing heat exchanger (CHX ® ). This device was operated under typical coal-fired flue gas conditions on a continuous basis for a period of approximately 10 months. Data from the test indicate that virtually no decrease in Teflon ® thickness was observed for the coating on the first two rows of heat exchanger tubes, even at high inlet particulate loadings. Evidence of wear was present only at the microscopic level, and even then was very minor in severity.

B.J. JANKURA; G.A. KUDLAC; R.T. BAILEY

1998-06-01T23:59:59.000Z

216

Oxyfuel CO2 compression: The gas phase reaction of elemental mercury and \\{NOx\\} at high pressure and absorption into nitric acid  

Science Journals Connector (OSTI)

Abstract Oxyfuel combustion is a technology which combusts coal in oxygen and recycled flue gas, producing a carbon dioxide rich flue gas for sequestration. Oxyfuel flue gas contains trace amounts of elemental mercury, which may corrode brazed aluminium heat exchangers used in the carbon dioxide purification system. International gas vendors have tested the use of the compression system to remove other flue gas impurities such as NOx; however, the reaction mechanism of mercury and its reaction products with \\{NOx\\} and nitric acid formed with condensed water vapour are unclear. This study used lab scale experiments to study the absorption of gaseous elemental mercury into nitric acid and the gas phase reaction between mercury and nitrogen dioxide formed from oxidised NO at pressures up to 25 bar. It was observed that mercury has limited absorption into nitric acid and may partially desorb out of solution after depressurisation. On the other hand, mercury reacted readily with nitrogen dioxide (formed from nitric oxide oxidation at high pressure) in the gas phase. These gas phase reactions from the oxidation of nitric oxide to nitrogen dioxide to the subsequent oxidation of elemental mercury by nitrogen dioxide were predicted using existing global kinetic equations. The limited absorption of gaseous elemental mercury in nitric acid and significant oxidation of gaseous elemental mercury by nitrogen dioxide suggests that the primary removal step for elemental mercury is through the gas phase reaction. Oxyfuel compression circuits should therefore allow sufficient residence time for this gas phase reaction to occur.

Timothy Ting; Rohan Stanger; Terry Wall

2014-01-01T23:59:59.000Z

217

NETL: News Release - DOE Seeks Cost-Shared Research Proposals to Remove  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

March 20, 2000 March 20, 2000 DOE Seeks Cost-Shared Research Proposals to Remove Mercury From Coal-Fired Power Plants With the Environmental Protection Agency expected to decide in December whether to regulate mercury emissions from coal-burning boilers, the U.S. Department of Energy has kicked off a new effort to develop more affordable pollution control technologies that can remove mercury from power plant flue gases. The Energy Department, through its National Energy Technology Laboratory, has issued a solicitation offering up to $13 million over three years for industry proposals on cost-cutting mercury-control methods for coal-based power systems. Currently no technology exists that can uniformly control mercury from power plant flue gas emissions. The effectiveness of existing flue gas emission controls in removing mercury can vary considerably from plant to plant, or even from boiler to boiler. With today's technologies, mercury removal can range from essentially no control to as high as 90 percent.

218

Windowed Carbon Nanotubes for Efficient CO2 Removal from Natural Gas  

E-Print Network [OSTI]

We demonstrate from molecular dynamics simulations that windowed carbon nanotubes can efficiently separate CO2 from the CO2/CH4 mixture, resembling polymeric hollow fibers for gas separation. Three CO2/CH4 mixtures with 30%, 50% and 80% CO2 are investigated as a function of applied pressure from 80 to 180 bar. In all simulated conditions, only CO2 permeation is observed; CH4 is completely rejected by the nitrogen-functionalized windows or pores on the nanotube wall in the accessible timescale, while maintaining a fast diffusion rate along the tube. The estimated time-dependent CO2 permeance ranges from 107 to 105 GPU (gas permeation unit), compared with ~100 GPU for typical polymeric membranes. CO2/CH4 selectivity is estimated to be ~108 from the difference in free-energy barriers of permeation. This work suggests that a windowed carbon nanotube can be used as a highly efficient medium, configurable in hollow-fiber-like modules, for removing CO2 from natural gas.

Liu, Hongjun; Dai, Sheng; Jiang, De-en; 10.1021/jz301576s

2012-01-01T23:59:59.000Z

219

Sorbents for High Temperature Removal of Arsenic from Coal-Derived Synthesis Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Gokhan O. Alptekin, PhD Robert Copeland, PhD Gokhan O. Alptekin, PhD Robert Copeland, PhD (Primary Contact) TDA Research, Inc TDA Research, Inc 12345 W. 52 nd Avenue 12345 W. 52 nd Avenue Wheat Ridge, CO 80033 Wheat Ridge, CO 80033 Email: copeland@tda.com Email: galptekin@tda.com Tel: (303) 940-2323 Tel: (303) 940-2349 Fax: (303) 422-7763 Fax: (303) 422-7763 Margarita Dubovik Yevgenia Gershanovich TDA Research, Inc TDA Research, Inc 12345 W. 52 nd Avenue 12345 W. 52 nd Avenue Wheat Ridge, CO 80033 Wheat Ridge, CO 80033 Email: dubovik@tda.com Email: ygershan@tda.com Tel: (303) 940-2316 Tel: (303) 940-2346 Fax: (303) 422-7763 Fax: (303) 422-7763 Sorbents for High Temperature Removal of Arsenic from Coal-Derived Synthesis Gas

220

Durable regenerable sorbent pellets for removal of hydrogen sulfide from coal gas  

DOE Patents [OSTI]

Pellets for removing hydrogen sulfide from a coal gasification stream at an elevated temperature are prepared in durable form usable over repeated cycles of absorption and regeneration. The pellets include a material reactive with hydrogen sulfide, in particular zinc oxide, a binder, and an inert material, in particular calcium sulfate (drierite), having a particle size substantially larger than other components of the pellets. A second inert material and a promoter may also be included. Preparation of the pellets may be carried out by dry, solid-state mixing of components, moistening the mixture, and agglomerating it into pellets, followed by drying and calcining. Pellet size is selected, depending on the type of reaction bed for which the pellets are intended. The use of inert material with a large particle size provides a stable pellet structure with increased porosity, enabling effective gas contact and prolonged mechanical durability.

Siriwardane, Ranjani V. (Morgantown, WV)

1997-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

Durable regenerable sorbent pellets for removal of hydrogen sulfide coal gas  

DOE Patents [OSTI]

Pellets for removing hydrogen sulfide from a coal gasification stream at an elevated temperature are prepared in durable form, usable over repeated cycles of absorption and regeneration. The pellets include a material reactive with hydrogen sulfide, in particular zinc oxide, a binder, and an inert material, in particular calcium sulfate (drierite), having a particle size substantially larger than other components of the pellets. A second inert material and a promoter may also be included. Preparation of the pellets may be carried out by dry, solid-state mixing of components, moistening the mixture, and agglomerating it into pellets, followed by drying and calcining. Pellet size is selected, depending on the type of reaction bed for which the pellets are intended. The use of inert material with a large particle size provides a stable pellet structure with increased porosity, enabling effective gas contact and prolonged mechanical durability.

Siriwardane, Ranjani V. (Morgantown, WV)

1999-01-01T23:59:59.000Z

222

Application of colloidal gas aphron suspensions produced from Sapindus mukorossi for arsenic removal from contaminated soil  

Science Journals Connector (OSTI)

Abstract Colloidal gas aphron dispersions (CGAs) can be described as a system of microbubbles suspended homogenously in a liquid matrix. This work examines the performance of \\{CGAs\\} in comparison to surfactant solutions for washing low levels of arsenic from an iron rich soil. Sodium Dodecyl Sulfate (SDS) and saponin, a biodegradable surfactant, obtained from Sapindus mukorossi or soapnut fruit were used for generating \\{CGAs\\} and solutions for soil washing. Column washing experiments were performed in down-flow and up flow modes at a soil pH of 5 and 6 using varying concentration of SDS and soapnut solutions as well as CGAs. Soapnut \\{CGAs\\} removed more than 70% arsenic while SDS \\{CGAs\\} removed up to 55% arsenic from the soil columns in the soil pH range of 5–6. \\{CGAs\\} and solutions showed comparable performances in all the cases. \\{CGAs\\} were more economical since it contains 35% of air by volume, thereby requiring less surfactant. Micellar solubilization and low pH of soapnut facilitated arsenic desorption from soil column. FT-IR analysis of effluent suggested that soapnut solution did not interact chemically with arsenic thereby facilitating the recovery of soapnut solution by precipitating the arsenic. Damage to soil was minimal arsenic confirmed by metal dissolution from soil surface and SEM micrograph.

Soumyadeep Mukhopadhyay; Sumona Mukherjee; Mohd. Ali Hashim; Bhaskar Sen Gupta

2015-01-01T23:59:59.000Z

223

Method and apparatus for removing non-condensible gas from a working fluid in a binary power system  

DOE Patents [OSTI]

Apparatus for removing non-condensible gas from a working fluid utilized in a thermodynamic system comprises a membrane having an upstream side operatively connected to the thermodynamic system so that the upstream side of the membrane receives a portion of the working fluid. The first membrane separates the non-condensible gas from the working fluid. A pump operatively associated with the membrane causes the portion of the working fluid to contact the membrane and to be returned to the thermodynamic system.

Mohr, Charles M. (Idaho Falls, ID); Mines, Gregory L. (Idaho Falls, ID); Bloomfield, K. Kit (Idaho Falls, ID)

2002-01-01T23:59:59.000Z

224

The use of activated charcoal for the removal of oxygen from gas ...  

Science Journals Connector (OSTI)

May 1, 1970 ... being analyzed by gas-solid chromatography. ... chosen for gas separations will not separate ... two or three stations had been processed to.

1999-12-27T23:59:59.000Z

225

Gas Turbine Plants  

Science Journals Connector (OSTI)

In a cycle process of a gas turbine, the compressor load, as well as ... from the expansion of the hot pressurized flue gas. Either turbine, compressor and driven assembly are joined by ... shaft is thus divided,...

1992-01-01T23:59:59.000Z

226

Flue gas desulfurization gypsum and fly ash  

SciTech Connect (OSTI)

The Cumberland Fossil Plant (CUF) is located in Stewart County, Tennessee, and began commercial operation in 1972. This is the Tennessee Valley Authority`s newest fossil (coal-burning) steam electric generating plant. Under current operating conditions, the plant burns approximately seven million tons of coal annually. By-products from the combustion of coal are fly ash, approximately 428,000 tons annually, and bottom ash, approximately 115,000 tons annually. Based on historical load and projected ash production rates, a study was initially undertaken to identify feasible alternatives for marketing, utilization and disposal of ash by-products. The preferred alternative to ensure that facilities are planned for all by-products which will potentially be generated at CUF is to plan facilities to handle wet FGD gypsum and dry fly ash. A number of different sites were evaluated for their suitability for development as FGD gypsum and ash storage facilities. LAW Engineering was contracted to conduct onsite explorations of sites to develop information on the general mature of subsurface soil, rock and groundwater conditions in the site areas. Surveys were also conducted on each site to assess the presence of endangered and threatened species, wetlands and floodplains, archaeological and cultural resources, prime farmland and other site characteristics which must be considered from an environmental perspective.

Not Available

1992-05-01T23:59:59.000Z

227

Recovery of CO2 from Flue Gases: Commercial Trends  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

CO CO 2 from Flue Gases: Commercial Trends Originally presented at the Canadian Society of Chemical Engineers annual meeting October 4-6, 1999, Saskatoon, Saskatchewan, Canada Authors: Dan G. Chapel (dan.chapel@fluor.com; 949-349-7530) Carl L. Mariz (carl.mariz@fluor.com; 949-349-7530) FluorDaniel One Fluor Drive Aliso Viejo CA, 92698 John Ernest (john.ernest@minimed.com; 818-576-4293) Advanced Quality Services Inc 11024 Balboa Blvd. PMB154, Granada Hills, CA 91344-5007 1 Recovery of CO 2 from Flue Gases: Commercial Trends Originally presented at the Canadian Society of Chemical Engineers annual meeting October 4-6, 1999, Saskatoon, Saskatchewan, Canada Authors: Dan Chapel - Fluor Daniel Inc., Senior Vice President Technology; Oil, Gas & Power John Ernest - Advanced Quality Services Inc., Validation Engineer

228

MERCURY REMOVAL IN A NON-THERMAL, PLASMA-BASED MULTI-POLLUTANT CONTROL TECHNOLOGY FOR UTILITY BOILERS  

SciTech Connect (OSTI)

Powerspan has conducted pilot scale testing of a multi-pollutant control technology at FirstEnergy's Burger Power Plant under a cooperative agreement with the U.S. Department of Energy. The technology, Electro-Catalytic Oxidation (ECO), simultaneously removes sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), fine particulate matter (PM{sub 2.5}) and mercury (Hg) from the flue gas of coal-fired power plants. Powerspan's ECO{reg_sign} pilot test program focused on optimization of Hg removal in a 1-MWe slipstream pilot while maintaining greater than 90% removal of NO{sub x} and 98% removal of SO{sub 2}. This Final Technical Report discusses pilot operations, installation and maintenance of the Hg SCEMS instrumentation, and performance results including component and overall removal efficiencies of SO{sub 2}, NO{sub x}, PM and Hg from the flue gas and removal of captured Hg from the co-product fertilizer stream.

Christopher R. McLaron

2004-12-01T23:59:59.000Z

229

On the Removal of Aluminide Coating from Blades of Gas Turbin Engine  

Science Journals Connector (OSTI)

The peculiarities of removing ????-11 coating from ??32 type alloy in an acidic etching bath depending on the concentration and ratio between the amounts of potassium bichromate and ammonium heptamolybdate additives

N. A. Amirkhanova; R. R. Nev'yantseva; A. A. Bybin; I. P. Semenova…

2003-09-01T23:59:59.000Z

230

Catalytic activity of oxidized (combusted) oil shale for removal of nitrogen oxides with ammonia as a reductant in combustion gas streams, Part 1  

SciTech Connect (OSTI)

Oxidized oil shale from the combustor in the LLNL hot recycle solids oil shale retorting process has been studied as a catalyst for removing nitrogen oxides from laboratory gas streams using NH{sub 3} as areductant. Combusted Green River oil shale heated at 10{degrees}C/min in an Ar/O{sub 2}/NO/NH{sub 3} mixture ({approximately}93%/6%/2000 ppm/4000 ppm) with a gas residence time of {approximately}0.6 sec exhibited NO removal between 250 and 500{degrees}C, with maximum removal of 70% at {approximately}400{degrees}C. Under isothermal conditions with the same gas mixture, the maximum NO removal was found to be {approximately}64%. When CO{sub 2} was added to the gas mixture at {approximately}8%, the NO removal dropped to {approximately}50%. However, increasing the gas residence time to {approximately}1.2 sec, increased NO removal to 63%. These results are not based on optimized process conditions, but indicate oxidized (combusted) oil shale is an effective catalyst for NO removal from combustion gas streams using NH{sub 3} as the reductant.

Reynolds, J.G.; Taylor, R.W.; Morris, C.J.

1992-06-10T23:59:59.000Z

231

Catalytic activity of oxidized (combusted) oil shale for removal of nitrogen oxides with ammonia as a reductant in combustion gas streams, Part 2  

SciTech Connect (OSTI)

Oxidized oil shale from the combustor in the LLNL Hot-Recycled-Solids (HRS) oil shale retorting process has been found to be a catalyst for removing nitrogen oxides from laboratory gas streams using NH{sub 3} as a reductant. Oxidized Green River oil shale heated at 10{degree}C/min in an Ar/O{sub 2}/NO/NH{sub 3} mixture ({approximately}93%/6%/2000 ppM/4000 ppM) with a gas residence time of {approximately}0.6 sec removed NO between 250 and 500{degree}C, with maximum removal of 70% at {approximately}400{degree}C. Under isothermal conditions with the same gas mixture, the maximum NO removal was {approximately}64%. When CO{sub 2} was added to the gas mixture at {approximately}8%, the NO removal dropped to {approximately}50%. However, increasing the gas residence time to {approximately}1.2 sec, increased NO removal to 63%. Nitrogen balances of these experiments suggest selective catalytic reduction of NO is occurring using NH{sub 3} as the reductant. These results are not based on completely optimized process conditions, but indicate oxidized oil shale is an effective catalyst for NO removal from combustion gas streams using NH{sub 3} as the reductant. Parameters calculated for implementing oxidized oil shale for NO{sub x} remediation on the current HRS retort indicate an abatement device is practical to construct.

Reynolds, J.G.; Taylor, R.W.; Morris, C.J.

1993-01-04T23:59:59.000Z

232

Catalytic activity of oxidized (combusted) oil shale for removal of nitrogen oxides with ammonia as a reductant in combustion gas streams, Part 2  

SciTech Connect (OSTI)

Oxidized oil shale from the combustor in the LLNL Hot-Recycled-Solids (HRS) oil shale retorting process has been found to be a catalyst for removing nitrogen oxides from laboratory gas streams using NH[sub 3] as a reductant. Oxidized Green River oil shale heated at 10[degree]C/min in an Ar/O[sub 2]/NO/NH[sub 3] mixture ([approximately]93%/6%/2000 ppM/4000 ppM) with a gas residence time of [approximately]0.6 sec removed NO between 250 and 500[degree]C, with maximum removal of 70% at [approximately]400[degree]C. Under isothermal conditions with the same gas mixture, the maximum NO removal was [approximately]64%. When CO[sub 2] was added to the gas mixture at [approximately]8%, the NO removal dropped to [approximately]50%. However, increasing the gas residence time to [approximately]1.2 sec, increased NO removal to 63%. Nitrogen balances of these experiments suggest selective catalytic reduction of NO is occurring using NH[sub 3] as the reductant. These results are not based on completely optimized process conditions, but indicate oxidized oil shale is an effective catalyst for NO removal from combustion gas streams using NH[sub 3] as the reductant. Parameters calculated for implementing oxidized oil shale for NO[sub x] remediation on the current HRS retort indicate an abatement device is practical to construct.

Reynolds, J.G.; Taylor, R.W.; Morris, C.J.

1993-01-04T23:59:59.000Z

233

Removal of Hydrogen Sulfide from Landfill Gas Using a Solar Regenerable Adsorbent.  

E-Print Network [OSTI]

??Landfill gas is a complex mix of gases, containing methane, carbon dioxide, nitrogen and hydrogen sulfide, created by the action of microorganisms within the landfill.… (more)

Kalapala, Sreevani

2014-01-01T23:59:59.000Z

234

FIELD DEMONSTRATION OF A MEMBRANE PROCESS TO RECOVER HEAVY HYDROCARBONS AND TO REMOVE WATER FROM NATURAL GAS  

SciTech Connect (OSTI)

The objective of this project is to design, construct and field demonstrate a 3-MMscfd membrane system to recover natural gas liquids (NGL) and remove water from raw natural gas. An extended field test to demonstrate system performance under real-world conditions is required to convince industry users of the efficiency and reliability of the process. The system will be designed and fabricated by Membrane Technology and Research, Inc. (MTR) and then installed and operated at British Petroleum (BP)-Amoco's Pascagoula, MS plant. The Gas Research Institute will partially support the field demonstration and BP-Amoco will help install the unit and provide onsite operators and utilities. The gas processed by the membrane system will meet pipeline specifications for dewpoint and Btu value and can be delivered without further treatment to the pipeline. Based on data from prior membrane module tests, the process is likely to be significantly less expensive than glycol dehydration followed by propane refrigeration, the principal competitive technology. At the end of this demonstration project the process will be ready for commercialization. The route to commercialization will be developed during this project and may involve collaboration with other companies already servicing the natural gas processing industry.

K.A. Lokhandwala; T. Hofmann; J. Kaschemekat; C. Bailey; M. Jacobs; R. Baker; Membrane Group

2000-04-04T23:59:59.000Z

235

FIELD DEMONSTRATION OF A MEMBRANE PROCESS TO RECOVER HEAVY HYDROCARBONS AND TO REMOVE WATER FROM NATURAL GAS  

SciTech Connect (OSTI)

The objective of this project is to design, construct and field demonstrate a 3-MMscfd membrane system to recover natural gas liquids (NGL) and remove water from raw natural gas. An extended field test to demonstrate system performance under real-world conditions is required to convince industry users of the efficiency and reliability of the process. The system will be designed and fabricated by Membrane Technology and Research, Inc. (MTR) and then installed and operated at British Petroleum (BP)-Amoco's Pascagoula, MS plant. The Gas Research Institute will partially support the field demonstration and BP-Amoco will help install the unit and provide onsite operators and utilities. The gas processed by the membrane system will meet pipeline specifications for dewpoint and Btu value and can be delivered without further treatment to the pipeline. Based on data from prior membrane module tests, the process is likely to be significantly less expensive than glycol dehydration followed by propane refrigeration, the principal competitive technology. At the end of this demonstration project the process will be ready for commercialization. The route to commercialization will be developed during this project and may involve collaboration with other companies already servicing the natural gas processing industry.

R. Baker; T. Hofmann; J. Kaschemekat; K.A. Lokhandwala; Membrane Group; Module Group; Systems Group

2001-01-11T23:59:59.000Z

236

Survey and Down-Selection of Acid Gas Removal Systems for the Thermochemical Conversion of Biomass to Ethanol with a Detailed Analysis of an MDEA System  

SciTech Connect (OSTI)

The first section (Task 1) of this report by Nexant includes a survey and screening of various acid gas removal processes in order to evaluate their capability to meet the specific design requirements for thermochemical ethanol synthesis in NREL's thermochemical ethanol design report (Phillips et al. 2007, NREL/TP-510-41168). MDEA and selexol were short-listed as the most promising acid-gas removal agents based on work described in Task 1. The second report section (Task 2) describes a detailed design of an MDEA (methyl diethanol amine) based acid gas removal system for removing CO2 and H2S from biomass-derived syngas. Only MDEA was chosen for detailed study because of the available resources.

Nexant, Inc., San Francisco, California

2011-05-01T23:59:59.000Z

237

A Comparative Economical Analysis of Technologies for CO2 Removal from Offshore Natural Gas  

Science Journals Connector (OSTI)

Abstract In the scenario of the Brazilian Pre-Salt fields, where associated Natural Gas (NG) shows high concentration of CO2, gas conditioning comes out as one of the main challenges. Among the possible capture technologies available, three alternatives stand out for CO2 sequestration: (A) gas permeation through membranes, (B) absorption columns using aqueous blends of ethanolamines and (C) application of hybrid - membrane modules in series with amine absorption and regeneration columns. The main objective of this work is to investigate the technical and economical feasibility of applying these three separation processes on offshore platforms, given the stringent constraints on footprint and equipment weight, and for minimizing NG production and transportation costs. The methodology involves: (i) development of cases based on the Brazilian Pre-Salt gas composition. NG streams with CO2 molar concentrations ranging from 8 to 18% are applied; (ii) Simulations of three process flowsheets, corresponding to each one of chosen technologies - A, B and C; (iii) Equipment sizing; and (iv) Analysis of economic performance through calculation of capital (CAPEX) and operational (OPEX) costs.

Tatiana S. Gadelha; Aline R.S. Guimarães; Andressa Nakao; Ofélia de Q.F. Araújo; José Luiz de Medeiros

2012-01-01T23:59:59.000Z

238

Multiple pollutant removal using the condensing heat exchanger. Task 3, Long term testing at the ECTC  

SciTech Connect (OSTI)

The objective of this task is to demonstrate long term operation of a condensing heat exchanger for coal-fired conditions. A small condensing heat exchanger will be installed at the Environmental Control Technology Center in Barker, New York. It will be installed downstream of the flue gas particulate removal system. The test will determine the amount of wear, if any, on the Teflon{trademark} covered internals of the heat exchanger. Visual inspection and measurements will be obtained for the Teflon{trademark} covered tubes during the test. The material wear study will conducted over a one year calendar period, and the CHX equipment will be operated to the fullest extent allowable.

Schulze, K.H.

1996-01-01T23:59:59.000Z

239

Utilization of Partially Gasified Coal for Mercury Removal  

SciTech Connect (OSTI)

In this project, General Electric Energy and Environmental Research Corporation (EER) developed a novel mercury (Hg) control technology in which the sorbent for gas-phase Hg removal is produced from coal in a gasification process in-situ at a coal burning plant. The main objective of this project was to obtain technical information necessary for moving the technology from pilot-scale testing to a full-scale demonstration. A pilot-scale gasifier was used to generate sorbents from both bituminous and subbituminous coals. Once the conditions for optimizing sorbent surface area were identified, sorbents with the highest surface area were tested in a pilot-scale combustion tunnel for their effectiveness in removing Hg from coal-based flue gas. It was determined that the highest surface area sorbents generated from the gasifier process ({approx}600 m{sup 2}/g) had about 70%-85% of the reactivity of activated carbon at the same injection rate (lb/ACF), but were effective in removing 70% mercury at injection rates about 50% higher than that of commercially available activated carbon. In addition, mercury removal rates of up to 95% were demonstrated at higher sorbent injection rates. Overall, the results of the pilot-scale tests achieved the program goals, which were to achieve at least 70% Hg removal from baseline emissions levels at 25% or less of the cost of activated carbon injection.

Chris Samuelson; Peter Maly; David Moyeda

2008-09-09T23:59:59.000Z

240

Low Cost Chemical Feedstocks Using an Improved and Energy Efficient Natural Gas Liquid (NGL) Removal Process, Final Technical Report  

SciTech Connect (OSTI)

The overall objective of this project is to develop a new low-cost and energy efficient Natural Gas Liquid (NGL) recovery process - through a combination of theoretical, bench-scale and pilot-scale testing - so that it could be offered to the natural gas industry for commercialization. The new process, known as the IROA process, is based on U.S. patent No. 6,553,784, which if commercialized, has the potential of achieving substantial energy savings compared to currently used cryogenic technology. When successfully developed, this technology will benefit the petrochemical industry, which uses NGL as feedstocks, and will also benefit other chemical industries that utilize gas-liquid separation and distillation under similar operating conditions. Specific goals and objectives of the overall program include: (i) collecting relevant physical property and Vapor Liquid Equilibrium (VLE) data for the design and evaluation of the new technology, (ii) solving critical R&D issues including the identification of suitable dehydration and NGL absorbing solvents, inhibiting corrosion, and specifying proper packing structure and materials, (iii) designing, construction and operation of bench and pilot-scale units to verify design performance, (iv) computer simulation of the process using commercial software simulation platforms such as Aspen-Plus and HYSYS, and (v) preparation of a commercialization plan and identification of industrial partners that are interested in utilizing the new technology. NGL is a collective term for C2+ hydrocarbons present in the natural gas. Historically, the commercial value of the separated NGL components has been greater than the thermal value of these liquids in the gas. The revenue derived from extracting NGLs is crucial to ensuring the overall profitability of the domestic natural gas production industry and therefore of ensuring a secure and reliable supply in the 48 contiguous states. However, rising natural gas prices have dramatically reduced the economic incentive to extract NGLs from domestically produced natural gas. Successful gas processors will be those who adopt technologies that are less energy intensive, have lower capital and operating costs and offer the flexibility to tailor the plant performance to maximize product revenue as market conditions change, while maintaining overall system efficiency. Presently, cryogenic turbo-expander technology is the dominant NGL recovery process and it is used throughout the world. This process is known to be highly energy intensive, as substantial energy is required to recompress the processed gas back to pipeline pressure. The purpose of this project is to develop a new NGL separation process that is flexible in terms of ethane rejection and can reduce energy consumption by 20-30% from current levels, particularly for ethane recoveries of less than 70%. The new process integrates the dehydration of the raw natural gas stream and the removal of NGLs in such a way that heat recovery is maximized and pressure losses are minimized so that high-value equipment such as the compressor, turbo-expander, and a separate dehydration unit are not required. GTI completed a techno-economic evaluation of the new process based on an Aspen-HYSYS simulation model. The evaluation incorporated purchased equipment cost estimates obtained from equipment suppliers and two different commercial software packages; namely, Aspen-Icarus and Preliminary Design and Quoting Service (PDQ$). For a 100 MMscfd gas processing plant, the annualized capital cost for the new technology was found to be about 10% lower than that of conventional technology for C2 recovery above 70% and about 40% lower than that of conventional technology for C2 recovery below 50%. It was also found that at around 40-50% C2 recovery (which is economically justifiable at the current natural gas prices), the energy cost to recover NGL using the new technology is about 50% of that of conventional cryogenic technology.

Meyer, Howard, S.; Lu, Yingzhong

2012-08-10T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
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241

Nitrogen removal from natural gas. Quarterly report, September 1, 1996--November 30, 1996  

SciTech Connect (OSTI)

Membrane processes have been considered for natural gas denitrogenation. The challenge, not yet overcome, is to develop membranes with the required methane/nitrogen separation characteristics. Our calculations show that a methane-permeate membrane with a methane/nitrogen selectivity of 4 to 6 would make a membrane denitrogenation process viable. Phase I of this project showed that this target selectivity can be achieved, and that the economics of processes based on this selectivity would be competitive. Gas permeation measurements with membranes prepared from two rubbery polymers and a superglassy polymer showed that two of these materials had the target selectivity of 4 to 6 when operated at temperatures below -20{degrees}C. An economic analysis showed that a process based on these membranes is competitive with other technologies for small streams containing less than 10% nitrogen. Hybrid designs combining membranes with other technologies are suitable for high-flow, high-nitrogen-content streams. The Phase I work demonstrated the potential usefulness of using methane-permeable membranes for the denitrogenation of natural gas. The objective of Phase II is to determine which of the two candidate membranes is the most suitable for scale up to membrane modules for laboratory tests followed by field tests of the process.

Wijmans, J.G.; Lokhandwala, K.A.; Ringer, M.B.

1996-12-31T23:59:59.000Z

242

SULFURIC ACID REMOVAL PROCESS EVALUATION: LONG-TERM RESULTS  

SciTech Connect (OSTI)

The objective of this project is to demonstrate the use of alkaline reagents injected into the furnace of coal-fired boilers as a means of controlling sulfuric acid emissions. The project is being co-funded by the U.S. DOE National Energy Technology Laboratory, under Cooperative Agreement DE-FC26-99FT40718, along with EPRI, the American Electric Power Company (AEP), FirstEnergy Corp., the Tennessee Valley Authority, and Dravo Lime, Inc. Sulfuric acid controls are becoming of increasing interest to power generators with coal-fired units for a number of reasons. Sulfuric acid is a Toxic Release Inventory species and can cause a variety of plant operation problems such as air heater plugging and fouling, back-end corrosion, and plume opacity. These issues will likely be exacerbated with the retrofit of selective catalytic reduction (SCR) for NO{sub x} control on many coal-fired plants, as SCR catalysts are known to further oxidize a portion of the flue gas SO{sub 2} to SO{sub 3}. The project previously tested the effectiveness of furnace injection of four different calcium-and/or magnesium-based alkaline sorbents on full-scale utility boilers. These reagents were tested during four one- to two-week tests conducted on two FirstEnergy Bruce Mansfield Plant (BMP) units. One of the sorbents tested was a magnesium hydroxide byproduct slurry produced from a modified Thiosorbic{reg_sign} Lime wet flue gas desulfurization system. The other three sorbents are available commercially and include dolomite, pressure-hydrated dolomitic lime, and commercial magnesium hydroxide. The dolomite reagent was injected as a dry powder through out-of-service burners, while the other three reagents were injected as slurries through air-atomizing nozzles inserted through the front wall of the upper furnace, either across from the nose of the furnace or across from the pendant superheater tubes. After completing the four one- to two-week tests, the most promising sorbents were selected for longer-term (approximately 25-day) full-scale tests on two different units. The longer-term tests were conducted to confirm the effectiveness of the sorbents tested over extended operation on two different boilers, and to determine balance-of-plant impacts. The first long-term test was conducted on FirstEnergy's BMP, Unit 3, and the second test was conducted on AEP's Gavin Plant, Unit 1. The Gavin Plant testing provided an opportunity to evaluate the effects of sorbent injected into the furnace on SO{sub 3} formed across an operating SCR reactor. This report presents the results from those long-term tests. The tests determined the effectiveness of injecting commercially available magnesium hydroxide slurry (Gavin Plant) and byproduct magnesium hydroxide slurry (both Gavin Plant and BMP) for sulfuric acid control. The results show that injecting either slurry could achieve up to 70 to 75% overall sulfuric acid removal. At BMP, this overall removal was limited by the need to maintain acceptable electrostatic precipitator (ESP) particulate control performance. At Gavin Plant, the overall sulfuric acid removal was limited because the furnace injected sorbent was less effective at removing SO{sub 3} formed across the SCR system installed on the unit for NOX control than at removing SO{sub 3} formed in the furnace. The long-term tests also determined balance-of-plant impacts from slurry injection during the two tests. These include impacts on boiler back-end temperatures and pressure drops, SCR catalyst properties, ESP performance, removal of other flue gas species, and flue gas opacity. For the most part the balance-of-plant impacts were neutral to positive, although adverse effects on ESP performance became an issue during the BMP test.

Gary M. Blythe; Richard McMillan

2002-07-03T23:59:59.000Z

243

The Development of Warm Gas Cleanup Technologies for the Removal of Sulfur Containing Species from Steam Hydrogasification  

E-Print Network [OSTI]

economic comparison of IGCC power plants with cold gas cleanup and hot gas cleanup units using Indian coals.

Luo, Qian

2012-01-01T23:59:59.000Z

244

Process studies for a new method of removing H/sub 2/S from industrial gas streams  

SciTech Connect (OSTI)

A process for the removal of hydrogen sulfide from coal-derived gas streams has been developed. The basis for the process is the absorption of H/sub 2/S into a polar organic solvent where it is reacted with dissolved sulfur dioxide to form elemental sulfur. After sulfur is crystallized from solution, the solvent is stripped to remove dissolved gases and water formed by the reaction. The SO/sub 2/ is generated by burning a portion of the sulfur in a furnace where the heat of combustion is used to generate high pressure steam. The SO/sub 2/ is absorbed into part of the lean solvent to form the solution necessary for the first step. The kinetics of the reaction between H/sub 2/S and SO/sub 2/ dissolved in mixtures of N,N-Dimethylaniline (DMA)/ Diethylene Glycol Monomethyl Ether and DMA/Triethylene Glycol Dimethyl Ether was studied by following the temperature rise in an adiabatic calorimeter. This irreversible reaction was found to be first-order in both H/sub 2/S and SO/sub 2/, with an approximates heat of reaction of 28 kcal/mole of SO/sub 2/. The sole products of the reaction appear to be elemental sulfur and water. The presence of DMA increases the value of the second-order rate constant by an order of magnitude over that obtained in the glycol ethers alone. Addition of other tertiary aromatic amines enhances the observed kinetics; heterocyclic amines (e.g., pyridine derivatives) have been found to be 10 to 100 times more effective as catalysts when compared to DMA.

Neumann, D.W.; Lynn, S.

1986-07-01T23:59:59.000Z

245

Reliability study of a special decay heat removal system of a gas-cooled fast reactor demonstrator  

Science Journals Connector (OSTI)

Abstract The European roadmap toward the development of generation IV concepts addresses the safety and reliability assessment of the special system designed for decay heat removal of a gas-cooled fast reactor demonstrator (GFRD). The envisaged system includes the combination of both active and passive means to accomplish the fundamental safety function. Failure probabilities are calculated on various system configurations, according to either pressurized or depressurized accident events under investigation, and integrated with probabilities of occurrence of corresponding hardware components and natural circulation performance assessment. The analysis suggests the improvement of measures against common cause failures (CCF), in terms of an appropriate diversification among the redundant systems, to reduce the system failure risk. Particular emphasis is placed upon passive system reliability assessment, being recognized to be still an open issue, and the approach based on the functional reliability is adopted to address the point. Results highlight natural circulation as a challenging factor for the decay heat removal safety function accomplishment by means of passive devices. With the models presented here, the simplifying assumptions and the limited scenarios considered according to the level of definition of the design, where many systems are not yet established, one can conclude that attention has to be paid to the functional aspects of the passive system, i.e. the ones not pertaining to the “hardware” of the system. In this article the results of the analysis are discussed, where the effects of the analytical assumptions, design options, accident managements on the reliability are examined. The design diversity of the components undergoing \\{CCFs\\} can be effective for the improvement and some accident management measures are also possible by making use of the long grace period in GFRD.

Luciano Burgazzi

2014-01-01T23:59:59.000Z

246

CHEMICAL PROCESS RESEARCH AND DEVELOPMENT PROGRAM. Chapter from the Energy and Environment Division Annual Report 1980  

E-Print Network [OSTI]

removal is flue- gas desulfurization, Under investigation are fundamental chemistry and transport mechanisms underlying reagent additive

Authors, Various

2014-01-01T23:59:59.000Z

247

Effect of ignition location on the in-process removal of combustion deposits from the output window of a gas turbine laser ignition system  

Science Journals Connector (OSTI)

The effect of ignition location on the effectiveness of combustion deposit removal from the reverse side of an optical window in a laser ignition system for use in gas turbines is presented. Such deposits consist of carbon and other by-products which accumulate on the walls of the chamber as a result of incomplete combustion. In laser based ignition systems this accumulation of combustion deposits has the potential to reduce the transmissive properties of the output window required for transmission of the laser radiation into the combustion chamber, adversely affecting the likelihood of successful ignition. In this work, a full empirical study into the in-process removal of combustion deposits from the reverse side of the optical window in a laser ignition system using a Q-switched Nd:YAG laser is presented, with an emphasis on the effect of ignition location on the effectiveness of combustion deposit removal. In addition, the mechanism of deposit removal is discussed.

J. Griffiths; J. Lawrence; P. Fitzsimons

2013-01-01T23:59:59.000Z

248

Pre-Combustion CO2 Removal System Â… Demonstration Unit  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Post-Combustion CO Post-Combustion CO 2 Capture System for Existing Coal-fired Power Plant Project Review (DE-FE-0007580) Gökhan Alptekin, PhD Ambal Jayaraman, PhD Robert Copeland, PhD DOE/NETL CO 2 Capture Technology Meeting Meeting Pittsburgh, PA July 8, 2013 TDA R e s e a r c h Project Summary * The objective is to develop a post-combustion capture process for coal-fired power plants and demonstrate technical feasibility (at bench-scale) and economic viability of the new concept * A mesoporous carbon adsorbent is used to selectively remove CO 2 from the flue gas, regenerating under very mild conditions Budget Period 1 * Sorbent Optimization/scale-up and Laboratory Evaluations * Process Design and System Analysis Budget Period 2 * Long-term Sorbent Cycling * Design of a Breadboard Prototype Test Unit

249

Gas Separations using Ceramic Membranes  

SciTech Connect (OSTI)

This project has been oriented toward the development of a commercially viable ceramic membrane for high temperature gas separations. A technically and commercially viable high temperature gas separation membrane and process has been developed under this project. The lab and field tests have demonstrated the operational stability, both performance and material, of the gas separation thin film, deposited upon the ceramic membrane developed. This performance reliability is built upon the ceramic membrane developed under this project as a substrate for elevated temperature operation. A comprehensive product development approach has been taken to produce an economically viable ceramic substrate, gas selective thin film and the module required to house the innovative membranes for the elevated temperature operation. Field tests have been performed to demonstrate the technical and commercial viability for (i) energy and water recovery from boiler flue gases, and (ii) hydrogen recovery from refinery waste streams using the membrane/module product developed under this project. Active commercializations effort teaming with key industrial OEMs and end users is currently underway for these applications. In addition, the gas separation membrane developed under this project has demonstrated its economical viability for the CO2 removal from subquality natural gas and landfill gas, although performance stability at the elevated temperature remains to be confirmed in the field.

Paul KT Liu

2005-01-13T23:59:59.000Z

250

NETL: IEP – Post-Combustion CO2 Emissions Control - CO2 Capture from Flue  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

from Flue Gas by Phase Transitional Absorption from Flue Gas by Phase Transitional Absorption Project No.: FG26-05NT42488 Basic Illustration of the Phase Transitional Absorption Process. Basic Illustration of the Phase Transitional Absorption Process. Hampton University researched a novel carbon dioxide (CO2) absorption concept, phase transitional absorption, that utilizes a two-part proprietary absorbent consisting of an activated agent dissolved in a solvent. Phase separation of the activated agent from the chemical solvent occurs during CO2 absorption and physical separation of the two phases exiting the absorber reduces the volume of process liquid requiring thermal regeneration. This unique aspect of phase transitional absorption also decreases the amount of energy (i.e., steam) required to liberate the CO2. If the proper liquid

251

Seawater desalination by gas hydrate process and removal characteristics of dissolved ions (Na+, K+, Mg2 +, Ca2 +, B3 +, Cl?, SO42 ?)  

Science Journals Connector (OSTI)

Abstract In order to evaluate hydrate-based desalination (HBD), experiments with seawater samples were carried out at various conditions (i.e. hydraulic pressure, washing step, and hydrate-forming gas). Before and after the hydrate process, cations (Na+, K+, Mg2 +, Ca2 +, and B3 +) and anions (Cl? and SO42 ?) were analyzed by inductively coupled plasma atomic emission spectroscopy (ICP-AES) and ion chromatography (IC). In a single stage of CO2 hydrate process without any pretreatment, 71%–94% of each cation was removed in the following order: K+ > Na+ ? Mg2 + ? Ca2 + > B3 + and 73%–83% of each anion was removed. When the brines on the surface of hydrate pellets were removed, the ion removal efficiency increased above 4%. It was also found that the desalting efficiency depended on the hydrate-forming gas (CO2 > CH4) and the hydraulic pressure (6–10 MPa) to produce hydrate pellets. In this study, the removal efficiency of cations and anions in a real seawater sample using HBD processes were reported for the first time.

Kyung Chan Kang; Praveen Linga; Kyeong-nam Park; Sang-June Choi; Ju Dong Lee

2014-01-01T23:59:59.000Z

252

A study of the effect of chloride on mercury removal in a fluidized bed combustion (FBC) system  

SciTech Connect (OSTI)

Mercury exists in three forms, which are elemental mercury, inorganic mercury compounds, and organic mercury. Each form of mercury has a very different exposure potential. Oxidized mercury is soluble and has a tendency to associate with particles. Nearly all the post-combustion flue gas cleaning systems proposed to remove mercury may be categorized as either scrubbers or adsorbers. Therefore, the mercury sink in the cleaning system will be either the excess water of a wet scrubber or the mercury laden sorbent from an absorber. The major problem for post-combustion mercury capture systems is capturing the practically water-insoluble elemental mercury. Co-firing with high chlorine coal or RDF in utility boiler systems can provide an HCI atmosphere for the oxidation of elemental mercury in flue gas at relatively low temperatures (500--600 C). The objective of this study is to increase the efficiency of mercury emission cleaning methods by using HCl to convert elemental mercury to oxidized mercury species at low monetary costs and lower other toxic air emissions. When high chlorine (0.3--0.5%) coals were burned and a high intensity vortex flow (from secondary air) was used, around 70% of the total mercury in the fuel was condensed and absorbed by the fly ash (including calcium compounds). The remaining 30% of total fuel mercury was emitted in the gas phase in the flue gas. As for the gas phase mercury, about 98% of it exists in an oxidized form with a higher boiling temperature than elemental mercury and can be easily captured by an ESP or FGP apparatus. Only about 0.5% of the total fuel mercury was released to the atmosphere in elemental form.

Liu, K.; Gao, Y.; Li, F.; Pan, W.P.; Riley, J.T.; Mehta, A.K.; Ho, K.K.; Smith, S.R.

2000-07-01T23:59:59.000Z

253

Gas separation process using membranes with permeate sweep to remove CO.sub.2 from gaseous fuel combustion exhaust  

DOE Patents [OSTI]

A gas separation process for treating exhaust gases from the combustion of gaseous fuels, and gaseous fuel combustion processes including such gas separation. The invention involves routing a first portion of the exhaust stream to a carbon dioxide capture step, while simultaneously flowing a second portion of the exhaust gas stream across the feed side of a membrane, flowing a sweep gas stream, usually air, across the permeate side, then passing the permeate/sweep gas back to the combustor.

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

2012-05-15T23:59:59.000Z

254

Test Plan to Demonstrate Removal of Iodine and Tritium from Simulated Nuclear Fuel Recycle Plant Off-gas Streams using Adsorption Processes  

SciTech Connect (OSTI)

This letter documents the completion of the FCR&D Level 4 milestone for the Sigma Team – Off-Gas - ORNL work package (FT-14OR031202), “Co-absorption studies - Design system complete/test plan complete” (M4FT-14OR0312022), due November 15, 2013. The objective of this test plan is to describe research that will determine the effectiveness of silver mordenite and molecular sieve beds to remove iodine and water (tritium) from off-gas streams arising from used nuclear fuel recycling processes, and to demonstrate that the iodine and water can be recovered separately from one another.

Bruffey, Stephanie H. [ORNL] [ORNL; Spencer, Barry B. [ORNL] [ORNL; Jubin, Robert Thomas [ORNL] [ORNL

2013-12-11T23:59:59.000Z

255

FlueGen Inc | Open Energy Information  

Open Energy Info (EERE)

FlueGen Inc FlueGen Inc Jump to: navigation, search Name FlueGen, Inc. Place Irvine, California Zip 92614 Product Irvine-based original equipment manufacturer (OEM) of air pollution control systems for the utility industry, including coal-fired power plants, in addition to financing client's projects, thereafter operating and maintaining the system for a fee. Coordinates 41.837752°, -79.268594° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":41.837752,"lon":-79.268594,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

256

Bubble inclusion and removal using PDMS membrane-based gas permeation for applications in pumping, valving and mixing in microfluidic devices  

Science Journals Connector (OSTI)

Several advancements in fluid handling applications of a gas-permeable polydimethylsiloxane (PDMS) membrane are demonstrated. Devices for controlled pumping, bubble injection, bubble removal and mixing are demonstrated using a three-layered fabrication method. The ability of a gas-permeable membrane to control flow in glass channels is determined. Consistent flow rates ranging from approximately 1 to 14 µl min?1 were observed using control pressures from 100 to 700 mbar. Bubble injection and removal from microfluidic channels was performed in monolithic PDMS devices using several bubble trap geometries at fluid flow rates over 100 µl min?1. The rate of removal of the air in the bubble trap was determined as a function of the area of membrane exposed and the applied vacuum. The PDMS membrane was shown to be an effective tool for the injection and removal of air bubbles in a method of enhancing mixing using bubbles and branched microchannels. The amount of mixing was optically determined before and after bubbles entered the fluid channel. The ability to produce all of these compatible components using a single fabrication process is a step toward inexpensive, parallel, highly integrated microfluidic systems with minimal external controls.

Michael Johnson; Greg Liddiard; Mark Eddings; Bruce Gale

2009-01-01T23:59:59.000Z

257

Developments in integrated pollutant removal for low-emission oxy-fuel combustion  

SciTech Connect (OSTI)

A complete coal combustion and flue gas treatment scheme was designed, constructed, and operated at bench scale as a product of cooperative research between US DOE’s Albany Research Center (ARC) and Jupiter Oxygen Corporation. The combustion gas generated using this oxy-fuel coal combustion process was effectively captured using an integrated pollutant removal (IPR) process. Supporting laboratory-scale research focuses on elements of IPR such as extraction of particulates, SO2, and mercury, and on the character of the liquid and vapor phase compositions for the CO2 - N2 - O2 mixture at the temperature and pressure conditions found at the end of the process. Future pilot-scale work will be necessary to generate economic and engineering data that will apply to full-scale oxy-fuel/IPR systems.

Gerdemann, Stephen J.; Summers, Cathy A.; Oryshchyn, Danylo B.; Patrick, Brian (Jupiter Oxygen Corp.); Ochs, Thomas L.

2005-09-01T23:59:59.000Z

258

Evaluation of gas-reburning and low NO{sub x} burners on a wall fired boiler. Progress report, January 1--March 31, 1996  

SciTech Connect (OSTI)

The primary objective of this Clean Coal Technology project is to evaluate the use of Gas Reburning and Low NO{sub x} Burners (GR-LNB) for NO{sub x} emission control from a wall fired boiler. This project is being conducted in three phases at the host site, a 172 MW{sub e} wall fired boiler of Public Service Company of Colorado, Cherokee Unit 3 in Denver, Colorado: Phase I, design and permitting has been completed on June 30, 1992; Phase II, construction and start-up has been completed on September 1991; and Phase III, operation, data collection, reporting and disposition. Phase III activities during this reporting period involved the following: compilation, analysis and assembly of the final report and initiation of restoration activities; restoration of the gas reburning system involving removal of the flue gas recirculation system (permanent Second Generation Gas Reburning); and participants meeting and reburning workshop. Long term testing of the equipment demonstrated an average NO{sub x} reduction of 65% using 18% gas heat input. After removing the flue gas recirculation system, (Second Generation GR), an average NO{sub x} of 64% was achieved using 13% gas heat input. The project goal of 70% reduction was achieved, but no on an average basis due to the load requirements of the utility.

NONE

1996-04-15T23:59:59.000Z

259

Optimal control system design of an acid gas removal unit for an IGCC power plants with CO2 capture  

SciTech Connect (OSTI)

Future IGCC plants with CO{sub 2} capture should be operated optimally in the face of disturbances without violating operational and environmental constraints. To achieve this goal, a systematic approach is taken in this work to design the control system of a selective, dual-stage Selexol-based acid gas removal (AGR) unit for a commercial-scale integrated gasification combined cycle (IGCC) power plant with pre-combustion CO{sub 2} capture. The control system design is performed in two stages with the objective of minimizing the auxiliary power while satisfying operational and environmental constraints in the presence of measured and unmeasured disturbances. In the first stage of the control system design, a top-down analysis is used to analyze degrees of freedom, define an operational objective, identify important disturbances and operational/environmental constraints, and select the control variables. With the degrees of freedom, the process is optimized with relation to the operational objective at nominal operation as well as under the disturbances identified. Operational and environmental constraints active at all operations are chosen as control variables. From the results of the optimization studies, self-optimizing control variables are identified for further examination. Several methods are explored in this work for the selection of these self-optimizing control variables. Modifications made to the existing methods will be discussed in this presentation. Due to the very large number of candidate sets available for control variables and due to the complexity of the underlying optimization problem, solution of this problem is computationally expensive. For reducing the computation time, parallel computing is performed using the Distributed Computing Server (DCS®) and the Parallel Computing® toolbox from Mathworks®. The second stage is a bottom-up design of the control layers used for the operation of the process. First, the regulatory control layer is designed followed by the supervisory control layer. Finally, an optimization layer is designed. In this paper, the proposed two-stage control system design approach is applied to the AGR unit for an IGCC power plant with CO{sub 2} capture. Aspen Plus Dynamics® is used to develop the dynamic AGR process model while MATLAB is used to perform the control system design and for implementation of model predictive control (MPC).

Jones, D.; Bhattacharyya, D.; Turton, R.; Zitney, S.

2012-01-01T23:59:59.000Z

260

Advanced Technology for the Capture of Carbon Dioxide from Flue Gases  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Technology for the Capture of Carbon Dioxide Technology for the Capture of Carbon Dioxide from Flue Gases by Shrikar Chakravarti (shrikar_chakravarti@praxair.com; 716-879-4760) Amitabh Gupta (ami_gupta@praxair.com; 716-879-2194) Balazs Hunek (balazs_hunek@praxair.com; 716-879-2250) Praxair, Inc. Process & Systems R&D, CO 2 Technology 175 East Park Drive, P.O. Box 44 Tonawanda, NY 14150 USA key words: flue gas, carbon dioxide, separation, amine absorption, oxygen tolerant process, amine blends First National Conference on Carbon Sequestration Washington, DC, May 15-17, 2001 Copyright 2001, Praxair Technology, Inc. All Rights Reserved. 1 Abstract Cost effective carbon sequestration schemes have been identified as a key need for dealing with carbon dioxide's (CO 2 ) impact on global climate change. Two main

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

Optimal Gas Turbine Integration to the Process Industries  

Science Journals Connector (OSTI)

Gas turbine integration can also help cut down flue gas emissions as a result of the improved efficiency of a cogeneration system. ... The aeroderivative turbines have higher efficiency than the industrial type, but they are more expensive. ...

Jussi Manninen; X. X. Zhu

1999-09-28T23:59:59.000Z

262

Process for removing a nitrogen gas from mixture comprising N/sub 2/ and CO or CO/sub 2/ and CO  

SciTech Connect (OSTI)

Processes are disclosed for removing N/sub 2/ from a feed gas comprising CO+N/sub 2/ or CO, CO/sub 2/+N/sub 2/ through PSA by using at least two adsorption columns containing an adsorbent exhibiting selective adsorb property to carbon monoxide which comprises: a step of pressurizing an adsorption column by the feed gas; a step of introducing the feed gas into the adsorption column, in which step was previously completed, so as to adsorb CO, or CO+CO/sub 2/ on or in the adsorbent; a step of connecting the adsorption column, in which step was previously completed, to the other adsorption column in which step was previously completed, to reduce the pressure in the former adsorption column to one atmosphere or a pressure close to it; a step of purging nitrogen by passing product gas through the adsorption column; a step of desorbing carbon monoxide adsorbed on or in the adsorbent of the adsorption column, by vacuum pump to recover a product gas; and a step of a connecting the adsorption column, in which step was previously completed, to the other adsorption column in which step was previously completed to increase pressure in the former column, periodically switching the flow between or among said adsorption columns so as to repeat the above steps in all the adsorption columns.

Matsui, S.; Hayashi, S.; Kumagai, M.; Tukahara, Y.

1984-08-28T23:59:59.000Z

263

Removing Cross-Border Capacity Bottlenecks in the European Natural Gas Market—A Proposed Merchant-Regulatory Mechanism  

Science Journals Connector (OSTI)

We propose a merchant-regulatory framework to promote investment in the European natural gas network infrastructure based on a price cap over two-part tariffs. As suggested by Vogelsang (J Regul Econ 20:141–165,

Anne Neumann; Juan Rosellón; Hannes Weigt

2014-11-01T23:59:59.000Z

264

Multiple pollutant removal using the condensing heat exchanger. Task 2, Pilot scale IFGT testing  

SciTech Connect (OSTI)

The purpose of Task 2 (IFGT Pilot-Scale Tests at the B&W Alliance Research Center) is to evaluate the emission reduction performance of the Integrated flue Gas Treatment (IFGT) process for coal-fired applications. The IFGT system is a two-stage condensing heat exchanger that captures multiple pollutants - while recovering waste heat. The IFGT technology offers the potential of a addressing the emission of SO{sub 2} and particulate from electric utilities currently regulated under the Phase I and Phase II requirements defined in Title IV, and many of the air pollutants that will soon be regulated under Title III of the Clean Air Act. The performance data will be obtained at pilot-scale conditions similar to full-scale operating systems. The task 2 IFGT tests have been designed to investigate several aspects of IFGT process conditions at a broader range of variable than would be feasible at a larger scale facility. The performance parameters that will be investigated are as follows: SO{sub 2} removal; particulate removal; removal of mercury and other heavy metals; NO{sub x} removal; HF and HCl removal; NH{sub 3} removal; ammonia-sulfur compounds generation; and steam injection for particle removal. For all of the pollutant removal tests, removal efficiency will be based on measurements at the inlet and outlet of the IFGT facility. Heat recovery measurements will also be made during these tests to demonstrate the heat recovery provided by the IFGT technology. This report provides the Final Test Plan for the first coal tested in the Task 2 pilot-scale IFGT tests.

Jankura, B.J.

1996-01-01T23:59:59.000Z

265

Continuous sulfur removal process  

DOE Patents [OSTI]

A continuous process for the removal of hydrogen sulfide from a gas stream using a membrane comprising a metal oxide deposited on a porous support is disclosed. 4 figures.

Jalan, V.; Ryu, J.

1994-04-26T23:59:59.000Z

266

Reducing the cost of CO{sub 2} capture from flue gases using membrane technology  

SciTech Connect (OSTI)

Studies of CO{sub 2} capture using membrane technology from coal-fired power-plant flue gas typically assume compression of the feed to achieve a driving force across the membrane. The high CO{sub 2} capture cost of these systems reflects the need to compress the low-pressure feed gas (1 bar) and the low CO{sub 2} purity of the product stream. This article investigates how costs for CO{sub 2} capture using membranes can be reduced by operating under vacuum conditions. The flue gas is pressurized to 1.5 bar, whereas the permeate stream is at 0.08 bar. Under these operating conditions, the capture cost is U.S. $54/tonne CO{sub 2} avoided compared to U.S. $82/tonne CO{sub 2} avoided using membrane processes with a pressurized feed. This is a. reduction of 35%. The article also investigates the effect on the capture cost of improvements in CO{sub 2} permeability and selectivity. The results show that the capture cost can be reduced to less than U.S. $25/tonne CO{sub 2} avoided when the CO{sub 2} permeability is 300 bar, CO{sub 2}/N{sub 2} selectivity is 250, and the membrane cost is U.S. $10/m{sup 2}.

Ho, M.T.; Allinson, G.W.; Wiley, D.E. [University of New South Wales, Kensington, NSW (Australia)

2008-03-15T23:59:59.000Z

267

PRODUCTION OF CONSTRUCTION AGGREGATES FROM FLUE GAS DESULFURIZATION SLUDGE  

SciTech Connect (OSTI)

The three main conclusions of this report are: (1) The pilot plant successfully demonstrated the continuous, fully-integrated, long-term process operation, including the mixing, pelletizing, and curing steps for aggregate production. The curing vessel, which was designed for the pilot plant test, was operated in a mass flow mode and performed well during pilot plant operation. (2) The pilot plant test demonstrated process flexibility. The same equipment was used to produce lightweight, medium-weight, and road aggregates. The only change was the mix formulation. Aggregates were produced from a variety of mix designs and from FGD sludge with solids concentrations between 45.0% and 56.7% and moisture contents between 55.0% and 43.3%. (3) The pilot plant provided operating data and experience to design and cost a commercial plant, which was not part of the cooperative agreement.

M.M. Wu; D.C. McCoy; R.O. Scandrol; M.L. Fenger; J.A. Withum; R.M. Statnick

2000-05-01T23:59:59.000Z

268

Combined Flue Gas Heat Recovery and Pollution Control Systems  

E-Print Network [OSTI]

in the field of heat recovery now make it possible to recover a portion of the wasted heat and improve the working conditions of the air purification equipment. Proper design and selection of heat recovery and pollution control equipment as a combination...

Zbikowski, T.

1979-01-01T23:59:59.000Z

269

Pilot-scale testing of a new sorbent for combined SO{sub 2}/NO{sub x} removal. Final report  

SciTech Connect (OSTI)

A new regenerable sorbent concept for SO{sub 2} and NOx removal was pilot-tested at Ohio Edison`s Edgewater generating station at a 1.5 to 2-MW(e) level. A radial panel-bed filter of a new dry, granular sorbent was exposed to flue gas and regenerated in an experimental proof-of-concept program. The project was successful in demonstrating the new sorbent`s ability to achieve 90% SO{sub 2} removal, 30% NOx removal, and over 80% removal of residual particulates with realistic approach temperatures and low pressure drops. Based on the results of this project, the retrofit cost of this technology is expected to be on the order of $400 per ton of SO{sub 2} and $900 per ton of NOx removed. This assumes that gas distribution is even and methane regeneration is used for a 30% average utilization. For a 2.5%-sulfur Ohio coal, this translates to a cost of approximately $17 per ton of coal. Two by-product streams were generated in the process that was tested: a solid, spent-sorbent stream and a highly-concentrated SO{sub 2} or elemental-sulfur stream. While not within the scope of the project, it was found possible to process these streams into useful products. The spent sorbent materials were shown to be excellent substrates for soil amendments; the elemental sulfur produced is innocuous and eminently marketable.

Nelson, S. Jr. [Sorbent Technologies Corp., Twinsburg, OH (United States)

1994-06-01T23:59:59.000Z

270

Multiple pollutant removal using the condensing heat exchanger: Preliminary test plan for Task 2, Pilot scale IFGT testing  

SciTech Connect (OSTI)

The purpose of Task 2 (IFGT Pilot-Scale Tests at the B&W Alliance Research Center) is to evaluate the emission reduction performance of the Integrated Flue Gas Treatment (IFGT) process for coal-fired applications. The IFGT system is a two-stage condensing heat exchanger that captures multiple pollutants -- while recovering waste heat. The IFGT technology offers the potential of addressing the emission of S0{sub 2} and particulate from electric utilities currently regulated under the Phase 1 and Phase 2 requirements defined in Title IV, and many of the air pollutants that will soon be regulated under Title III of the Clean Air Act. The performance data will be obtained at pilot-scale conditions similar to full-scale operating systems. The Task 2 IFGT tests have been designed to investigate several aspects of IFGT process conditions at a broader range of variables than would be feasible at a larger scale facility. The data from these tests greatly expands the IFGT performance database for coals and is needed for the technology to progress from the component engineering phase to system integration and commercialization. The performance parameters that will be investigated are as follows: SO{sub 2} removal; particulate removal; removal of mercury and other heavy metals; NO{sub x} removal; HF and HCl removal; NH{sub 3} removal; ammonia-sulfur compounds generation; and steam injection for particle removal. For all of the pollutant removal tests, removal efficiency will be based on measurements at the inlet and outlet of the IFGT facility. Heat recovery measurements will also be made during these tests to demonstrate the heat recovery provided by the IFGT technology. This report provides a preliminary test plan for all of the Task 2 pilot-scale IFGT tests.

Jankura, B.J.

1995-11-01T23:59:59.000Z

271

SULFURIC ACID REMOVAL PROCESS EVALUATION: SHORT-TERM RESULTS  

SciTech Connect (OSTI)

The objective of this project is to demonstrate the use of alkaline reagents injected into the furnace of coal-fired boilers as a means of controlling sulfuric acid emissions. Sulfuric acid controls are becoming of increasing interest to utilities with coal-fired units for a number of reasons. Sulfuric acid is a Toxic Release Inventory species, a precursor to acid aerosol/condensable emissions, and can cause a variety of plant operation problems such as air heater plugging and fouling, back-end corrosion, and plume opacity. These issues will likely be exacerbated with the retrofit of SCR for NOX control on some coal-fired plants, as SCR catalysts are known to further oxidize a portion of the flue gas SO{sub 2} to SO{sub 3}. The project is testing the effectiveness of furnace injection of four different calcium- and/or magnesium-based alkaline sorbents on full-scale utility boilers. These reagents have been tested during four one- to two-week tests conducted on two FirstEnergy Bruce Mansfield Plant units. One of the sorbents tested was a magnesium hydroxide slurry produced from a wet flue gas desulfurization system waste stream, from a system that employs a Thiosorbic{reg_sign} Lime scrubbing process. The other three sorbents are available commercially and include dolomite, pressure-hydrated dolomitic lime, and commercial magnesium hydroxide. The dolomite reagent was injected as a dry powder through out-of-service burners, while the other three reagents were injected as slurries through air-atomizing nozzles into the front wall of upper furnace, either across from the nose of the furnace or across from the pendant superheater tubes. After completing the four one- to two-week tests, the most promising sorbents were selected for longer-term (approximately 25-day) full-scale tests. The longer-term tests are being conducted to confirm the effectiveness of the sorbents tested over extended operation and to determine balance-of-plant impacts. This reports presents the results of the short-term tests; the long-term test results will be reported in a later document. The short-term test results showed that three of the four reagents tested, dolomite powder, commercial magnesium hydroxide slurry, and byproduct magnesium hydroxide slurry, were able to achieve 90% or greater removal of sulfuric acid compared to baseline levels. The molar ratio of alkali to flue gas sulfuric acid content (under baseline conditions) required to achieve 90% sulfuric acid removal was lowest for the byproduct magnesium hydroxide slurry. However, this result may be confounded because this was the only one of the three slurries tested with injection near the top of the furnace across from the pendant superheater platens. Injection at the higher level was demonstrated to be advantageous for this reagent over injection lower in the furnace, where the other slurries were tested.

Gary M. Blythe; Richard McMillan

2002-03-04T23:59:59.000Z

272

SULFURIC ACID REMOVAL PROCESS EVALUATION: SHORT-TERM RESULTS  

SciTech Connect (OSTI)

The objective of this project is to demonstrate the use of alkaline reagents injected into the furnace of coal-fired boilers as a means of controlling sulfuric acid emissions. Sulfuric acid controls are becoming of increasing interest to utilities with coal-fired units for a number of reasons. Sulfuric acid is a Toxic Release Inventory species, a precursor to acid aerosol/condensable emissions, and can cause a variety of plant operation problems such as air heater plugging and fouling, back-end corrosion, and plume opacity. These issues will likely be exacerbated with the retrofit of SCR for NO{sub x} control on some coal-fired plants, as SCR catalysts are known to further oxidize a portion of the flue gas SO{sub 2} to SO{sub 3}. The project is testing the effectiveness of furnace injection of four different calcium- and/or magnesium-based alkaline sorbents on full-scale utility boilers. These reagents have been tested during four one- to two-week tests conducted on two First Energy Bruce Mansfield Plant units. One of the sorbents tested was a magnesium hydroxide slurry produced from a wet flue gas desulfurization system waste stream, from a system that employs a Thiosorbic{reg_sign} Lime scrubbing process. The other three sorbents are available commercially and include dolomite, pressure-hydrated dolomitic lime, and commercial magnesium hydroxide. The dolomite reagent was injected as a dry powder through out-of-service burners, while the other three reagents were injected as slurries through air-atomizing nozzles into the front wall of upper furnace, either across from the nose of the furnace or across from the pendant superheater tubes. After completing the four one- to two-week tests, the most promising sorbents were selected for longer-term (approximately 25-day) full-scale tests. The longer-term tests are being conducted to confirm the effectiveness of the sorbents tested over extended operation and to determine balance-of-plant impacts. This reports presents the results of the short-term tests; the long-term test results will be reported in a later document. The short-term test results showed that three of the four reagents tested, dolomite powder, commercial magnesium hydroxide slurry, and byproduct magnesium hydroxide slurry, were able to achieve 90% or greater removal of sulfuric acid compared to baseline levels. The molar ratio of alkali to flue gas sulfuric acid content (under baseline conditions) required to achieve 90% sulfuric acid removal was lowest for the byproduct magnesium hydroxide slurry. However, this result may be confounded because this was the only one of the three slurries tested with injection near the top of the furnace across from the pendant superheater platens. Injection at the higher level was demonstrated to be advantageous for this reagent over injection lower in the furnace, where the other slurries were tested.

Gary M. Blythe; Richard McMillan

2002-02-04T23:59:59.000Z

273

Simultaneous Removal of NOx and Mercury in Low Temperature Selective Catalytic and Adsorptive Reactor  

SciTech Connect (OSTI)

The results of a 18-month investigation to advance the development of a novel Low Temperature Selective Catalytic and Adsorptive Reactor (LTSCAR), for the simultaneous removal of NO{sub x} and mercury (elemental and oxidized) from flue gases in a single unit operation located downstream of the particulate collectors, are reported. In the proposed LTSCAR, NO{sub x} removal is in a traditional SCR mode but at low temperature, and, uniquely, using carbon monoxide as a reductant. The concomitant capture of mercury in the unit is achieved through the incorporation of a novel chelating adsorbent. As conceptualized, the LTSCAR will be located downstream of the particulate collectors (flue gas temperature 140-160 C) and will be similar in structure to a conventional SCR. That is, it will have 3-4 beds that are loaded with catalyst and adsorbent allowing staged replacement of catalyst and adsorbent as required. Various Mn/TiO{sub 2} SCR catalysts were synthesized and evaluated for their ability to reduce NO at low temperature using CO as the reductant. It has been shown that with a suitably tailored catalyst more than 65% NO conversion with 100% N{sub 2} selectivity can be achieved, even at a high space velocity (SV) of 50,000 h-1 and in the presence of 2 v% H{sub 2}O. Three adsorbents for oxidized mercury were developed in this project with thermal stability in the required range. Based on detailed evaluations of their characteristics, the mercaptopropyltrimethoxysilane (MPTS) adsorbent was found to be most promising for the capture of oxidized mercury. This adsorbent has been shown to be thermally stable to 200 C. Fixed-bed evaluations in the targeted temperature range demonstrated effective removal of oxidized mercury from simulated flue gas at very high capacity ({approx}>58 mg Hg/g adsorbent). Extension of the capability of the adsorbent to elemental mercury capture was pursued with two independent approaches: incorporation of a novel nano-layer on the surface of the chelating mercury adsorbent to achieve in situ oxidation on the adsorbent, and the use of a separate titania-supported manganese oxide catalyst upstream of the oxidized mercury adsorbent. Both approaches met with some success. It was demonstrated that the concept of in situ oxidation on the adsorbent is viable, but the future challenge is to raise the operating capacity beyond the achieved limit of 2.7 mg Hg/g adsorbent. With regard to the manganese dioxide catalyst, elemental mercury was very efficiently oxidized in the absence of sulfur dioxide. Adequate resistance to sulfur dioxide must be incorporated for the approach to be feasible in flue gas. A preliminary benefits analysis of the technology suggests significant potential economic and environmental advantages.

Neville G. Pinto; Panagiotis G. Smirniotis

2006-03-31T23:59:59.000Z

274

Multiple pollutant removal using the condensing heat exchanger: Phase 1 final report, November 1995--June 1997. Addendum 2: Task 3 topical report -- Long term wear test  

SciTech Connect (OSTI)

Long-term operation of a condensing heat exchanger under typical coal-fired flue gas conditions was investigated in Phase 1, Task 3 of the Multiple Pollutant Removal Using the Condensing Heat Exchanger test program. The specific goal of this task was to determine the amount of wear, if any, on the Teflon{reg_sign}-covered heat transfer tubes in a condensing heat exchanger. A pilot-scale single-stage condensing heat exchanger (CHX{reg_sign}) was operated under typical coal-fired flue gas conditions on a continuous basis for a period of approximately 10 months. Operating conditions and particulate loadings for the test unit were monitored, Teflon{reg_sign} film thickness measurements were conducted, and surface replications (which duplicate the surface finish at the microscopic level) were taken at various times during the test. Data from the test indicate that virtually no decrease in Teflon{reg_sign} thickness was observed for the coating on the first two rows of heat exchanger tubes, even at high inlet particulate loadings (400 mg/dscm [0.35 lb/10{sup 6} Btu]). Evidence of wear was present only at the microscopic level, and even then was very minor in severity. Operation at high inlet particulate loadings resulted in accumulated ash deposits within the heat exchanger. Installation of a modified (higher flow rate) wash nozzle manifold substantially reduced subsequent deposit formation.

Kudlac, G.A.

1998-06-01T23:59:59.000Z

275

Simultaneous removal of H2S and COS using Zn-based solid sorbents in the bench-scale continuous hot gas desulfurization system integrated with a coal gasifier  

Science Journals Connector (OSTI)

A bench-scale continuous hot gas desulfurization system using Zn-based solid sorbents was developed to remove H2S and COS simultaneously in a 110 Nm3.../h of real coal-gasified syngas. The bench-scale unit, which...

Young Cheol Park; Sung-Ho Jo; Ho-Jung Ryu…

2012-12-01T23:59:59.000Z

276

Integrated capture of fossil fuel gas pollutants including CO.sub.2 with energy recovery  

DOE Patents [OSTI]

A method of reducing pollutants exhausted into the atmosphere from the combustion of fossil fuels. The disclosed process removes nitrogen from air for combustion, separates the solid combustion products from the gases and vapors and can capture the entire vapor/gas stream for sequestration leaving near-zero emissions. The invention produces up to three captured material streams. The first stream is contaminant-laden water containing SO.sub.x, residual NO.sub.x particulates and particulate-bound Hg and other trace contaminants. The second stream can be a low-volume flue gas stream containing N.sub.2 and O.sub.2 if CO2 purification is needed. The final product stream is a mixture comprising predominantly CO.sub.2 with smaller amounts of H.sub.2O, Ar, N.sub.2, O.sub.2, SO.sub.X, NO.sub.X, Hg, and other trace gases.

Ochs, Thomas L. (Albany, OR); Summers, Cathy A. (Albany, OR); Gerdemann, Steve (Albany, OR); Oryshchyn, Danylo B. (Philomath, OR); Turner, Paul (Independence, OR); Patrick, Brian R. (Chicago, IL)

2011-10-18T23:59:59.000Z

277

Control of pollutants in flue gases and fuel gases  

E-Print Network [OSTI]

and gasification technologies for heat and power . . . . . . . . 2-3 2.4 Waste incineration and waste . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1 2.2 Flue gases and fuel gases: combustion, gasification, pyrolysis, incineration and other . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3 3.3 Formation of sulphur compounds during combustion and gasification . 3-5 3.4 Emission

Laughlin, Robert B.

278

Control of pollutants in flue gases and fuel gases  

E-Print Network [OSTI]

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1 2.2 Flue gases and fuel gases: combustion, gasification, pyrolysis, incineration and other and gasification technologies for heat and power . . . . . . . . 2-3 2.4 Waste incineration and waste . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3 3.3 Formation of sulphur compounds during combustion and gasification . . 3-5 3.4 Emission

Zevenhoven, Ron

279

Contaminant trap for gas-insulated apparatus  

DOE Patents [OSTI]

A resinous body is placed in gas-insulated electrical apparatus to remove particulate material from the insulating gas.

Adcock, J.L.; Pace, M.O.; Christophorou, L.G.

1984-01-01T23:59:59.000Z

280

Reducing nitrogen oxides emissions from the combustion of LCV gas staged firing  

E-Print Network [OSTI]

with cotton gin tr ash, one of the primary fuels under consider ation, r esulted in flue NO levels ranging from 650-B60 ng/J (1. 5-2. 0 lb/MBtu). The Texas Air Control Board (TACB) will issue a facility a permit to operate only if NOx emissions are within... NO Methods of NOx Control Methods of NOx control may be lumped into two cate- gories: flue gas treatment (FGT) and combustion modifica- tion. The different processes are described below. Flue Gas Tr eatment Most of the research on FGT to date has been...

Finch, Stanley Frank

2012-06-07T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

Sensor placement algorithm development to maximize the efficiency of acid gas removal unit for integrated gasification combined cycle (IGCC) power plant with CO{sub 2} capture  

SciTech Connect (OSTI)

Future integrated gasification combined cycle (IGCC) power plants with CO{sub 2} capture will face stricter operational and environmental constraints. Accurate values of relevant states/outputs/disturbances are needed to satisfy these constraints and to maximize the operational efficiency. Unfortunately, a number of these process variables cannot be measured while a number of them can be measured, but have low precision, reliability, or signal-to-noise ratio. In this work, a sensor placement (SP) algorithm is developed for optimal selection of sensor location, number, and type that can maximize the plant efficiency and result in a desired precision of the relevant measured/unmeasured states. In this work, an SP algorithm is developed for an selective, dual-stage Selexol-based acid gas removal (AGR) unit for an IGCC plant with pre-combustion CO{sub 2} capture. A comprehensive nonlinear dynamic model of the AGR unit is developed in Aspen Plus Dynamics® (APD) and used to generate a linear state-space model that is used in the SP algorithm. The SP algorithm is developed with the assumption that an optimal Kalman filter will be implemented in the plant for state and disturbance estimation. The algorithm is developed assuming steady-state Kalman filtering and steady-state operation of the plant. The control system is considered to operate based on the estimated states and thereby, captures the effects of the SP algorithm on the overall plant efficiency. The optimization problem is solved by Genetic Algorithm (GA) considering both linear and nonlinear equality and inequality constraints. Due to the very large number of candidate sets available for sensor placement and because of the long time that it takes to solve the constrained optimization problem that includes more than 1000 states, solution of this problem is computationally expensive. For reducing the computation time, parallel computing is performed using the Distributed Computing Server (DCS®) and the Parallel Computing® toolbox from Mathworks®. In this presentation, we will share our experience in setting up parallel computing using GA in the MATLAB® environment and present the overall approach for achieving higher computational efficiency in this framework.

Paul, P.; Bhattacharyya, D.; Turton, R.; Zitney, S.

2012-01-01T23:59:59.000Z

282

Sensor placement algorithm development to maximize the efficiency of acid gas removal unit for integrated gasifiction combined sycle (IGCC) power plant with CO2 capture  

SciTech Connect (OSTI)

Future integrated gasification combined cycle (IGCC) power plants with CO{sub 2} capture will face stricter operational and environmental constraints. Accurate values of relevant states/outputs/disturbances are needed to satisfy these constraints and to maximize the operational efficiency. Unfortunately, a number of these process variables cannot be measured while a number of them can be measured, but have low precision, reliability, or signal-to-noise ratio. In this work, a sensor placement (SP) algorithm is developed for optimal selection of sensor location, number, and type that can maximize the plant efficiency and result in a desired precision of the relevant measured/unmeasured states. In this work, an SP algorithm is developed for an selective, dual-stage Selexol-based acid gas removal (AGR) unit for an IGCC plant with pre-combustion CO{sub 2} capture. A comprehensive nonlinear dynamic model of the AGR unit is developed in Aspen Plus Dynamics® (APD) and used to generate a linear state-space model that is used in the SP algorithm. The SP algorithm is developed with the assumption that an optimal Kalman filter will be implemented in the plant for state and disturbance estimation. The algorithm is developed assuming steady-state Kalman filtering and steady-state operation of the plant. The control system is considered to operate based on the estimated states and thereby, captures the effects of the SP algorithm on the overall plant efficiency. The optimization problem is solved by Genetic Algorithm (GA) considering both linear and nonlinear equality and inequality constraints. Due to the very large number of candidate sets available for sensor placement and because of the long time that it takes to solve the constrained optimization problem that includes more than 1000 states, solution of this problem is computationally expensive. For reducing the computation time, parallel computing is performed using the Distributed Computing Server (DCS®) and the Parallel Computing® toolbox from Mathworks®. In this presentation, we will share our experience in setting up parallel computing using GA in the MATLAB® environment and present the overall approach for achieving higher computational efficiency in this framework.

Paul, P.; Bhattacharyya, D.; Turton, R.; Zitney, S.

2012-01-01T23:59:59.000Z

283

Using carbon adsorbents for removing nitrogen oxides and sulphur oxides from flue gases  

Science Journals Connector (OSTI)

The use of carbon adsorbents in industrial power engineering outside Russia is briefly reviewed and the results of our own experimental investigations, made in the laboratory and at a pilot commercial installation, are given. The proposal to use the described device in a KE-25-24-C industrial boiler is outlined.

A.I. Blokhin; A.N. Nikitin; A.O. Gabibov

2003-01-01T23:59:59.000Z

284

earlier-awards | netl.doe.gov  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

SEQURE((tm)) Tracer Technology THIEF Process for the Removal of Mercury from Flue Gas. Co-developerscontributors include Nalco Mobotec. Clay-Liquid CO2 Removal Sorbent....

285

Reducing the cost of CO{sub 2} capture from flue gases using pressure swing adsorption  

SciTech Connect (OSTI)

Pressure swing adsorption (PSA) processes have been used extensively for gas separation, especially in the separation of hydrogen from CO{sub 2}, and in air purification. The objective of this paper is to examine the economic feasibility of pressure swing adsorption (PSA) for recovering CO{sub 2} from postcombustion power plant flue gas. The analysis considers both high-pressure feed and vacuum desorption using commercial adsorbent 13X, which has a working capacity of 2.2 mol/kg and CO{sub 2}/N{sub 2} selectivity of 54. The results show that using vacuum desorption reduces the capture cost from US$57 to US$51 per ton of CO{sub 2} avoided and is comparable in cost to CO{sub 2} capture using conventional MEA absorption of US$49 per ton of CO{sub 2} avoided. In this paper, a sensitivity analysis is also presented showing the effect on the capture cost with changes in process cycle; feed pressure and evacuation pressure; improvements the adsorbent characteristics; and selectivity and working capacity. The results show that a hypothetical adsorbent with a working capacity of 4.3 mol/kg and a CO{sub 2}/N{sub 2} selectivity of 150 can reduce the capture cost to US$30 per ton of CO{sub 2} avoided.

Ho, M.T.; Allinson, G.W.; Wiley, D.E. [University of New South Wales, Sydney, NSW (Australia)

2008-07-15T23:59:59.000Z

286

Removing an impediment to oil and gas leasing of certain federal lands in Corpus Christi, TX, and Port Hueneme, CA, and for other purposes. House of Representatives, Ninety-Eight Congress, Second Session  

SciTech Connect (OSTI)

With the addition of three technical ammendments, the Committee on Interior and Insular Affairs favors passage of H.R. 5787, a bill that removes a restriction to oil and gas leasing on naval air station lands within the city limits of Corpus Christi, Texas and Port Hueneme, California. Recognizing the controversial nature of competitive versus noncompetitive bidding, the committee stipulates that the land must be within a known geologic structure to use noncompetitive bidding. Additional views of three committee members follow the formal report and transmittal letter.

Not Available

1984-01-01T23:59:59.000Z

287

Evaluation of Gas Reburning and Low N0x Burners on a Wall Fired Boiler  

SciTech Connect (OSTI)

Under the U.S. Department of Energy's Clean Coal Technology Program (Round 3), a project was completed to demonstrate control of boiler emissions that comprise acid rain precursors, especially NOX. The project involved operating gas reburning technology combined with low NO, burner technology (GR-LNB) on a coal-fired utility boiler. Low NOX burners are designed to create less NOX than conventional burners. However, the NO, control achieved is in the range of 30-60-40, and typically 50%. At the higher NO, reduction levels, CO emissions tend to be higher than acceptable standards. Gas Reburning (GR) is designed to reduce the level of NO. in the flue gas by staged fuel combustion. When combined, GR and LNBs work in harmony to both minimize NOX emissions and maintain an acceptable level of CO emissions. The demonstration was performed at Public Service Company of Colorado's (PSCO) Cherokee Unit 3, located in Denver, Colorado. This unit is a 172 MW. wall-fired boiler that uses Colorado bituminous, low-sulfur coal and had a pre GR-LNB baseline NOX emission of 0.73 lb/1 Oe Btu. The target for the project was a reduction of 70 percent in NOX emissions. Project sponsors included the U.S. Department of Energy, the Gas Research Institute, Public Service Company of Colorado, Colorado Interstate Gas, Electric Power Research Institute, and the Energy and Environmental Research Corporation (EER). EER conducted a comprehensive test demonstration program over a wide range of boiler conditions. Over 4,000 hours of operation were achieved. Intensive measurements were taken to quantify the reductions in NOX emissions, the impact on boiler equipment and operability, and all factors influencing costs. The results showed that GR-LNB technology achieved excellent emission reductions. Although the performance of the low NOX burners (supplied by others) was somewhat less than expected, a NOX reduction of 65% was achieved at an average gas heat input of 180A. The performance goal of 70% reduction was met on many test runs, but at higher gas heat inputs. The impact on boiler equipment was determined to be very minimal. Toward the end of the testing, the flue gas recirculation (used to enhance gas penetration into the furnace) system was removed and new high pressure gas injectors were installed. Further, the low NOX burners were modified and gave better NO. reduction performance. These modifications resulted in a similar NO, reduction performance (64%) at a reduced level of gas heat input (-13Yo). In addition, the OFA injectors were re-designed to provide for better control of CO emissions. Although not a part of this project, the use of natural gas as the primary fuel with gas reburning was also tested. The gas/gas reburning tests demonstrated a reduction in NOX emissions of 43% (0.30 lb/1 OG Btu reduced to 0.17 lb/1 OG Btu) using 7% gas heat input. Economics are a key issue affecting technology development. Application of GR-LNB requires modifications to existing power plant equipment and as a result, the capital and operating costs depend largely on site-specific factors such as: gas availability at the site, gas to coal delivered price differential, sulfur dioxide removal requirements, windbox pressure, existing burner throat diameters, and reburn zone residence time available. Based on the results of this CCT project, EER expects that most GR-LNB installations will achieve at least 60% NOX control when firing 10-15% gas. The capital cost estimate for installing a GR-LNB system on a 300 MW, unit is approximately $25/kW. plus the cost of a gas pipeline (if required). Operating costs are almost entirely related to the differential cost of the natural gas compared to coal.

None

1998-09-01T23:59:59.000Z

288

Laboratory scale studies of Pd/{gamma}-Al{sub 2}O{sub 3} sorbents for the removal of trace contaminants from coal-derived fuel gas at elevated temperatures  

SciTech Connect (OSTI)

The Integrated Gasification Combined Cycle (IGCC) is a promising technology for the use of coal in a clean and efficient manner. In order to maintain the overall efficiency of the IGCC process, it is necessary to clean the fuel gas of contaminants (sulfur, trace compounds) at warm (150–540 °C) to hot (>540 °C) temperatures. Current technologies for trace contaminant (such as mercury) removal, primarily activated carbon based sorbents, begin to lose effectiveness above 100 °C, creating the need to develop sorbents effective at elevated temperatures. As trace elements are of particular environmental concern, previous work by this group has focused on the development of a Pd/?-Al{sub 2}O{sub 3} sorbent for Hg removal. This paper extends the research to Se (as hydrogen selenide, H{sub 2}Se), As (as arsine, AsH{sub 3}), and P (as phosphine, PH{sub 3}) which thermodynamic studies indicate are present as gaseous species under gasification conditions. Experiments performed under ambient conditions in He on 20 wt.% Pd/?-Al{sub 2}O{sub 3} indicate the sorbent can remove the target contaminants. Further work is performed using a 5 wt.% Pd/?-Al{sub 2}O{sub 3} sorbent in a simulated fuel gas (H{sub 2}, CO, CO{sub 2}, N{sub 2} and H{sub 2}S) in both single and multiple contaminant atmospheres to gauge sorbent performance characteristics. The impact of H{sub 2}O, Hg and temperature on sorbent performance is explored.

Rupp, Erik C.; Granite, Evan J. [U.S. DOE; Stanko, Dennis C. [U.S. DOE

2013-01-01T23:59:59.000Z

289

GAS INJECTION/WELL STIMULATION PROJECT  

SciTech Connect (OSTI)

Driver Production proposes to conduct a gas repressurization/well stimulation project on a six well, 80-acre portion of the Dutcher Sand of the East Edna Field, Okmulgee County, Oklahoma. The site has been location of previous successful flue gas injection demonstration but due to changing economic and sales conditions, finds new opportunities to use associated natural gas that is currently being vented to the atmosphere to repressurize the reservoir to produce additional oil. The established infrastructure and known geological conditions should allow quick startup and much lower operating costs than flue gas. Lessons learned from the previous project, the lessons learned form cyclical oil prices and from other operators in the area will be applied. Technology transfer of the lessons learned from both projects could be applied by other small independent operators.

John K. Godwin

2005-12-01T23:59:59.000Z

290

The potential for clean energy production using oxy-fuel combustion and integrated pollutant removal  

SciTech Connect (OSTI)

Effective remediation of flue gas produced by an oxy-fuel coal combustion process has been proven at bench scale in the course of cooperative research between USDOE’s Albany Research Center (ARC) and Jupiter Oxygen Corporation. All combustion gas pollutants were captured, including CO2 which was compressed to a liquefied state suitable for sequestration. Current laboratory-scale research and the future of combined oxy-fuel/IPR systems are discussed.

Ochs, Thomas L.; Oryshchyn, Danylo B.; Weber, Thomas (Jupiter Oxygen Corporation, Schiller Park, IL 60176).; Summers, Cathy A.

2005-05-01T23:59:59.000Z

291

Enahancing the Use of Coals by Gas Reburning - Sorbent Injection Volume 5 - Guideline Manual  

SciTech Connect (OSTI)

The purpose of the Guideline Manual is to provide recommendations for the application of combined gas reburning-sorbent injection (GR-SI) technologies to pre-NSPS boilers. The manual includes design recommendations, performance predictions, economic projections and comparisons with competing technologies. The report also includes an assessment of boiler impacts. Two full-scale demonstrations of gas reburning-sorbent injection form the basis of the Guideline Manual. Under the U.S. Department of Energy's Clean Coal Technology Program (Round 1), a project was completed to demonstrate control of boiler emissions that comprise acid rain precursors, specifically oxides of nitrogen (NOX) and sulfur dioxide (S02). Other project sponsors were the Gas Research Institute and the Illinois State Department of Commerce and Community Affairs. The project involved demonstrating the combined use of Gas Reburning and Sorbent Injection (GR-SI) to assess the air emissions reduction potential of these technologies.. Three potential coal-fired utility boiler host sites were evaluated: Illinois Power's tangentially-fired 71 MWe (net) Hennepin Unit W, City Water Light and Power's cyclone- fired 33 MWe (gross) Lakeside Unit #7, and Central Illinois Light Company's wall-fired 117 MWe (net) Edwards Unit #1. Commercial demonstrations were completed on the Hennepin and Lakeside Units. The Edwards Unit was removed from consideration for a site demonstration due to retrofit cost considerations. Gas Reburning (GR) controls air emissions of NOX. Natural gas is introduced into the furnace hot flue gas creating a reducing reburning zone to convert NOX to diatomic nitrogen (N,). Overfire air is injected into the furnace above the reburning zone to complete the combustion of the reducing (fuel) gases created in the reburning zone. Sorbent Injection (S1) consists of the injection of dry, calcium-based sorbents into furnace hot flue gas to achieve S02 capture. At each site where the techno!o@es were to be demonstrated, petiormance goals were set to achieve air emission reductions of 60 percent for NO. and 50 percent for SO2. These performance goals were exceeded during long term demonstration testing. For the tangentially fired unit, NOX emissions were reduced by 67.2% and S02 emissions by 52.6%. For the cyclone-fired unit, NOX emissions were reduced by 62.9% and SOZ emissions by 57.9%.

None

1998-09-01T23:59:59.000Z

292

Enhancing the Use of Coals by Gas Reburning - Sorbent Injection Volume 5 - Guideline Manual  

SciTech Connect (OSTI)

The purpose of the Guideline Manual is to provide recommendations for the application of combined gas reburning-sorbent injection (GR-SI) technologies to pre-NSPS boilers. The manual includes design recommendations, performance predictions, economic projections and comparisons with competing technologies. The report also includes an assessment of boiler impacts. Two full-scale demonstrations of gas reburning-sorbent injection form the basis of the Guideline Manual. Under the U.S. Department of Energy's Clean Coal Technology Program (Round 1), a project was completed to demonstrate control of boiler emissions that comprise acid rain precursors, specifically oxides of nitrogen (NOX) and sulfur dioxide (S02). Other project sponsors were the Gas Research Institute and the Illinois State Department of Commerce and Community Affairs. The project involved d,emonstrating the combined use of Gas Reburning and Sorbent Injection (GR-SI) to assess the air emissions reduction potential of these technologies.. Three potential coal-fired utility boiler host sites were evaluated: Illinois Power's tangentially-fired 71 MWe (net) Hennepin Unit #1, City Water Light and Power's cyclone- fired 33 MWe (gross) Lakeside Unit #7, and Central Illinois Light Company's wall-fired 117 MWe (net) Edwards Unit #1. Commercial demonstrations were completed on the Hennepin and Lakeside Units. The Edwards Unit was removed from consideration for a site demonstration due to retrofit cost considerations. Gas Reburning (GR) controls air emissions of NOX. Natural gas is introduced into the furnace hot flue gas creating a reducing reburning zone to convert NOX to diatomic nitrogen (N,). Overfire air is injected into the furnace above the reburning zone to complete the combustion of the reducing (fuel) gases created in the reburning zone. Sorbent Injection (S1) consists of the injection of dry, calcium-based sorbents into furnace hot flue gas to achieve S02 capture. `At each site where the technologies were to be demonstrated, performance goals were set to achieve air emission reductions of 60 percent for NOX and 50 percent for S02. These performance goals were exceeded during long term demonstration testing. For the tangentially fired unit, NO, emissions were reduced by 67.2?40 and SOZ emissions by 52.6Y0. For the cyclone-fired unit, NO, emissions were reduced by 62.9% and SOZ emissions by 57.9Y0.

None

1998-06-01T23:59:59.000Z

293

Load Preheating Using Flue Gases from a Fuel-Fired Heating System  

Broader source: Energy.gov [DOE]

This tip sheet discusses how the thermal efficiency of a process heating system can be improved significantly by using heat contained in furnace flue gases to preheat the furnace load.

294

Silica Scaling Removal Process  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Silica Scaling Removal Process Silica Scaling Removal Process Scientists at Los Alamos National Laboratory have developed a novel technology to remove both dissolved and colloidal...

295

Regenerable MgO-based sorbent for high temperature CO2 removal from syngas: 3. CO2 capture and sorbent enhanced water gas shift reaction  

Science Journals Connector (OSTI)

Abstract Regenerable MgO-based sorbent, which was prepared and evaluated in the thermogravimetric analyzer (TGA) in part 1, was also evaluated in high-pressure packed-bed unit in CO2/N2/H2O mixture and simulated pre-combustion syngas environment. In CO2/N2/H2O environment, the CO2 absorption capacity of the sorbent increases with increasing temperatures from 6.7% at 350 °C to 9.5% 450 °C. The sorbent is capable of achieving over 95% CO2 capture and 40% conversion in the water gas shift (WGS) reaction, which should be attributed to positive effect of WGS reaction in producing CO2 during the process. The sorbent reactivity and absorption capacity toward CO2, as well as its WGS catalytic activity decreases with increasing temperature. The maximum pre-breakthrough WGS conversion occurs at 350 °C, which diminishes as the sorbent is carbonated. The variable diffusivity shrinking core reaction model coupled with the two-fluid computational fluid dynamics (CFD) model was shown to accurately predict the break-through gas compositions at different operating conditions.

Emadoddin Abbasi; Armin Hassanzadeh; Shahin Zarghami; Hamid Arastoopour; Javad Abbasian

2014-01-01T23:59:59.000Z

296

Improving the Field Performance of Natural Gas Furnaces, Chicago, Illinois (Fact Sheet)  

SciTech Connect (OSTI)

The objective of this project is to examine the impact that common installation practices and age-induced equipment degradation may have on the installed performance of natural gas furnaces, as measured by steady-state efficiency and AFUE. PARR identified twelve furnaces of various ages and efficiencies that were operating in residential homes in the Des Moines Iowa metropolitan area and worked with a local HVAC contractor to retrieve them and test them for steady-state efficiency and AFUE in the lab. Prior to removal, system airflow, static pressure, equipment temperature rise, and flue loss measurements were recorded for each furnace. After removal from the field the furnaces were transported to the Gas Technology Institute (GTI) laboratory, where PARR conducted steady-state efficiency and AFUE testing. The test results show that steady-state efficiency in the field was 6.4% lower than that measured for the same furnaces under standard conditions in the lab, which included tuning the furnace input and air flow rate. Comparing AFUE measured under ASHRAE standard conditions with the label value shows no reduction in efficiency for the furnaces in this study over their 15 to 24 years of operation when tuned to standard conditions. Further analysis of the data showed no significant correlation between efficiency change and the age or the rated efficiency of the furnace.

Rothgeb, S.; Brand, L.

2013-11-01T23:59:59.000Z

297

Multipollutant Removal with WOWClean® System  

E-Print Network [OSTI]

such as petcoke, coal, wood, diesel and natural gas. In addition to significant removal of CO2, test results demonstrate the capability to reduce 99.5% SOx (from levels as high as 2200 ppm), 90% reduction of NOx, and > 90% heavy metals. The paper will include...

Romero, M.

2010-01-01T23:59:59.000Z

298

Efficiency of Gas-to-Liquids Technology with Different Synthesis Gas Production Methods  

Science Journals Connector (OSTI)

The design and optimization of a gas-to-liquids technology (GTL) is considered, mostly from the view of an optimal choice of a synthesis gas (syngas) production method. ... If the tail gas is not enough, an additional portion of the natural gas is burned. ... The temperature of the flue gases passing from the radiation chamber of the tubular furnace to the convection chamber is taken as equal to 1150 °C, which allows proper calculation of required amount of gas supplied to the burner. ...

Ilya S. Ermolaev; Vadim S. Ermolaev; Vladimir Z. Mordkovich

2014-02-05T23:59:59.000Z

299

Carbon dioxide capture from power or process plant gases  

SciTech Connect (OSTI)

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.

Bearden, Mark D; Humble, Paul H

2014-06-10T23:59:59.000Z

300

Chapter Nine - Gas Sweetening  

Science Journals Connector (OSTI)

Abstract This chapter begins by reviewing the processing of natural gas to meet gas sales contract specifications. It then describes acid gas limitations for pipelines and gas plants, before detailing the most common acid gas removal processes, such as solid-bed, chemical solvent processes, physical solvent processes, direct conversion processes, distillation process, and gas permeation processes. The chapter discusses the selection of the appropriate removal process for a given situation, and it provides a detailed design procedure for a solid-bed and chemical solvent process. The chapter ends by supplying a sample design for a solid-bed and chemical solvent process.

Maurice I. Stewart Jr.

2014-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

EGR Cooler Fouling- Visualization of Deposition and Removal Mechanis  

Broader source: Energy.gov [DOE]

Presents experimental data on exhaust gas recirculation(EGR) cooler fouling using new test apparatus that allows for in-situ observation of deposition and removal processes

302

Synthesis and development of processes for the recovery of sulfur from acid gases. Part 1, Development of a high-temperature process for removal of H{sub 2}S from coal gas using limestone -- thermodynamic and kinetic considerations; Part 2, Development of a zero-emissions process for recovery of sulfur from acid gas streams  

SciTech Connect (OSTI)

Limestone can be used more effectively as a sorbent for H{sub 2}S in high-temperature gas-cleaning applications if it is prevented from undergoing calcination. Sorption of H{sub 2}S by limestone is impeded by sintering of the product CaS layer. Sintering of CaS is catalyzed by CO{sub 2}, but is not affected by N{sub 2} or H{sub 2}. The kinetics of CaS sintering was determined for the temperature range 750--900{degrees}C. When hydrogen sulfide is heated above 600{degrees}C in the presence of carbon dioxide elemental sulfur is formed. The rate-limiting step of elemental sulfur formation is thermal decomposition of H{sub 2}S. Part of the hydrogen thereby produced reacts with CO{sub 2}, forming CO via the water-gas-shift reaction. The equilibrium of H{sub 2}S decomposition is therefore shifted to favor the formation of elemental sulfur. The main byproduct is COS, formed by a reaction between CO{sub 2} and H{sub 2}S that is analogous to the water-gas-shift reaction. Smaller amounts of SO{sub 2} and CS{sub 2} also form. Molybdenum disulfide is a strong catalyst for H{sub 2}S decomposition in the presence of CO{sub 2}. A process for recovery of sulfur from H{sub 2}S using this chemistry is as follows: Hydrogen sulfide is heated in a high-temperature reactor in the presence of CO{sub 2} and a suitable catalyst. The primary products of the overall reaction are S{sub 2}, CO, H{sub 2} and H{sub 2}O. Rapid quenching of the reaction mixture to roughly 600{degrees}C prevents loss Of S{sub 2} during cooling. Carbonyl sulfide is removed from the product gas by hydrolysis back to CO{sub 2} and H{sub 2}S. Unreacted CO{sub 2} and H{sub 2}S are removed from the product gas and recycled to the reactor, leaving a gas consisting chiefly of H{sub 2} and CO, which recovers the hydrogen value from the H{sub 2}S. This process is economically favorable compared to the existing sulfur-recovery technology and allows emissions of sulfur-containing gases to be controlled to very low levels.

Towler, G.P.; Lynn, S.

1993-05-01T23:59:59.000Z

303

In situ removal of contamination from soil  

DOE Patents [OSTI]

A process of remediation of cationic heavy metal contamination from soil utilizes gas phase manipulation to inhibit biodegradation of a chelating agent that is used in an electrokinesis process to remove the contamination. The process also uses further gas phase manipulation to stimulate biodegradation of the chelating agent after the contamination has been removed. The process ensures that the chelating agent is not attacked by bioorganisms in the soil prior to removal of the contamination, and that the chelating agent does not remain as a new contaminant after the process is completed. 5 figs.

Lindgren, E.R.; Brady, P.V.

1997-10-14T23:59:59.000Z

304

New configurations of a heat recovery absorption heat pump integrated with a natural gas boiler for boiler efficiency improvement  

SciTech Connect (OSTI)

Conventional natural gas-fired boilers exhaust flue gas direct to the atmosphere at 150 200 C, which, at such temperatures, contains large amount of energy and results in relatively low thermal efficiency ranging from 70% to 80%. Although condensing boilers for recovering the heat in the flue gas have been developed over the past 40 years, their present market share is still less than 25%. The major reason for this relatively slow acceptance is the limited improvement in the thermal efficiency of condensing boilers. In the condensing boiler, the temperature of the hot water return at the range of 50 60 C, which is used to cool the flue gas, is very close to the dew point of the water vapor in the flue gas. Therefore, the latent heat, the majority of the waste heat in the flue gas, which is contained in the water vapor, cannot be recovered. This paper presents a new approach to improve boiler thermal efficiency by integrating absorption heat pumps with natural gas boilers for waste heat recovery (HRAHP). Three configurations of HRAHPs are introduced and discussed. The three configurations are modeled in detail to illustrate the significant thermal efficiency improvement they attain. Further, for conceptual proof and validation, an existing hot water-driven absorption chiller is operated as a heat pump at operating conditions similar to one of the devised configurations. An overall system performance and economic analysis are provided for decision-making and as evidence of the potential benefits. These three configurations of HRAHP provide a pathway to achieving realistic high-efficiency natural gas boilers for applications with process fluid return temperatures higher than or close to the dew point of the water vapor in the flue gas.

Qu, Ming [Purdue University, West Lafayette, IN; Abdelaziz, Omar [ORNL; Yin, Hongxi [Southeast University, Nanjing, China

2014-01-01T23:59:59.000Z

305

Acidic gas capture by diamines  

DOE Patents [OSTI]

Compositions and methods related to the removal of acidic gas. In particular, the present disclosure relates to a composition and method for the removal of acidic gas from a gas mixture using a solvent comprising a diamine (e.g., piperazine) and carbon dioxide. One example of a method may involve a method for removing acidic gas comprising contacting a gas mixture having an acidic gas with a solvent, wherein the solvent comprises piperazine in an amount of from about 4 to about 20 moles/kg of water, and carbon dioxide in an amount of from about 0.3 to about 0.9 moles per mole of piperazine.

Rochelle, Gary (Austin, TX); Hilliard, Marcus (Missouri City, TX)

2011-05-10T23:59:59.000Z

306

bectcom-comrem | netl.doe.gov  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

(Dec 1997) Comprehensive Report to Congress Comprehensive Report to Congress on the Clean Coal Technology Program: Commercial Demonstration of the NOXSO SO2NOx Removal Flue Gas...

307

Polycyclic aromatic hydrocarbon emission profiles and removal efficiency by electrostatic precipitator and wetfine scrubber in an iron ore sintering plant  

SciTech Connect (OSTI)

A monitoring campaign of polychlorinated dibenzo-p-dioxins and dibenzofurans, polyaromatic hydrocarbons (PAHs), and polychlorinated biphenyl was carried out in an Italian iron ore sintering plant by sampling the combustion gases at the electrostatic precipitator (ESP) outlet, at the Wetfine scrubber (WS) outlet, and by collecting the ESP dust. Few data are available on these micropollutants produced in iron ore sintering plants, particularly from Italian plants. This study investigates the PAH emission profiles and the removal efficiency of ESPs and WS. PAHs were determined at the stack, ESP outlet flue gases, and in ESP dust to characterize the emission profiles and the performance of the ESP and the WS for reducing PAH emission. The 11 PAHs monitored are listed in the Italian legislative decree 152/2006. The mean total PAH sum concentration in the stack flue gases is 3.96 {mu}g/N m{sup 3}, in ESP outlet flue gases is 9.73 {mu}g/N m{sup 3}, and in ESP dust is 0.53 {mu}g/g. Regarding the emission profiles, the most abundant compound is benzo(b)fluoranthene, which has a relative low BaP toxic equivalency factors (TEF) value, followed by dibenzo(a,l)pyrene, which has a very high BaP(TEF) value. The emission profiles in ESP dust and in the flue gases after the ESP show some changes, whereas the fingerprint in ESP and stack flue gases is very similar. The removal efficiency of the ESP and of WS on the total PAH concentration is 5.2 and 59.5%, respectively. 2 figs., 5 tabs.

Ettore Guerriero; Antonina Lutri; Rosanna Mabilia; Maria Concetta Tomasi Sciano; Mauro Rotatori [Istituto sull'Inquinamento Atmosferico, Monterotondo Scalo (Italy). Consiglio Nazionale delle Ricerche

2008-11-15T23:59:59.000Z

308

Pilot-scale study of the effect of selective catalytic reduction catalyst on mercury speciation in Illinois and Powder River Basin coal combustion flue gases  

SciTech Connect (OSTI)

A study was conducted to investigate the effect of selective catalytic reduction (SCR) catalyst on mercury (Hg) speciation in bituminous and subbituminous coal combustion flue gases. Three different Illinois Basin bituminous coals (from high to low sulfur (S) and chlorine (Cl)) and one Powder River Basin (PRB) subbituminous coal with very low S and very low Cl were tested in a pilot-scale combustor equipped with an SCR reactor for controlling nitrogen oxides (NO{sub x}) emissions. The SCR catalyst induced high oxidation of elemental Hg (Hg{sup 0}), decreasing the percentage of Hg{sup 0} at the outlet of the SCR to values <12% for the three Illinois coal tests. The PRB coal test indicated a low oxidation of Hg{sup 0} by the SCR catalyst, with the percentage of Hg{sup 0} decreasing from {approximately} 96% at the inlet of the reactor to {approximately} 80% at the outlet. The low Cl content of the PRB coal and corresponding low level of available flue gas Cl species were believed to be responsible for low SCR Hg oxidation for this coal type. The test results indicated a strong effect of coal type on the extent of Hg oxidation. 16 refs., 4 figs., 3 tabs.

Lee, C.W.; Srivastava, R.K.; Ghorishi, S.B.; Karwowski, J.; Hastings, T.H.; Hirschi, J.C. [US Environmental Protection Agency, Triangle Park, NC (United States)

2006-05-15T23:59:59.000Z

309

Nonhydrocarbon Gases Removed from Natural Gas  

U.S. Energy Information Administration (EIA) Indexed Site

6-2013 6-2013 Federal Offshore Gulf of Mexico NA NA NA NA NA NA 1997-2013 Louisiana NA NA NA NA NA NA 1996-2013 New Mexico NA NA NA NA NA NA 1996-2013 Oklahoma NA NA NA NA NA NA 1996-2013 Texas NA NA NA NA NA NA 1991-2013 Wyoming NA NA NA NA NA NA 1991-2013 Other States Other States Total NA NA NA NA NA NA 1996-2013 Alabama NA NA NA NA NA NA 1991-2013 Arizona NA NA NA NA NA NA 1996-2013 Arkansas NA NA NA NA NA NA 1991-2013 California NA NA NA NA NA NA 1996-2013 Colorado NA NA NA NA NA NA 1996-2013 Florida NA NA NA NA NA NA 1996-2013 Illinois NA NA NA NA NA NA 1991-2013 Indiana NA NA NA NA NA NA 1991-2013 Kansas NA NA NA NA NA NA 1996-2013 Kentucky NA NA NA NA NA NA 1991-2013 Maryland

310

Nonhydrocarbon Gases Removed from Natural Gas  

U.S. Energy Information Administration (EIA) Indexed Site

661,168 718,674 721,507 836,698 867,922 761,836 1973-2012 661,168 718,674 721,507 836,698 867,922 761,836 1973-2012 Alaska 0 0 0 0 0 0 1996-2012 Federal Offshore Gulf of Mexico 0 0 0 0 0 0 1997-2012 Louisiana 0 0 0 0 1996-2010 Louisiana Onshore NA NA NA NA NA NA 2003-2012 Louisiana State Offshore NA NA NA NA NA NA 2003-2012 New Mexico 28,962 32,444 33,997 40,191 39,333 38,358 1980-2012 Oklahoma 0 0 0 0 1996-2010 Texas 254,337 241,626 240,533 279,981 284,557 183,118 1980-2012 Texas Onshore 254,337 241,626 240,533 279,981 284,557 183,118 1992-2012 Texas State Offshore NA 0 0 0 0 0 2003-2012 Wyoming 154,157 161,952 155,366 164,221 152,421 151,288 1980-2012 Other States Other States Total 223,711 282,651 291,611 352,304 1994-2010 Alabama 16,529 17,394 16,658 14,418 18,972 NA 1980-2012

311

Nonhydrocarbon Gases Removed from Natural Gas (Summary)  

U.S. Energy Information Administration (EIA) Indexed Site

1-2013 1-2013 Alaska NA NA NA NA NA NA 1996-2013 Arizona NA NA NA NA NA NA 1996-2013 Arkansas NA NA NA NA NA NA 1991-2013 California NA NA NA NA NA NA 1996-2013 Colorado NA NA NA NA NA NA 1996-2013 Florida NA NA NA NA NA NA 1996-2013 Illinois NA NA NA NA NA NA 1991-2013 Indiana NA NA NA NA NA NA 1991-2013 Kansas NA NA NA NA NA NA 1996-2013 Kentucky NA NA NA NA NA NA 1991-2013 Louisiana NA NA NA NA NA NA 1996-2013 Maryland NA NA NA NA NA NA 1991-2013 Michigan NA NA NA NA NA NA 1996-2013 Mississippi NA NA NA NA NA NA 1991-2013 Missouri NA NA NA NA NA NA 1991-2013 Montana NA NA NA NA NA NA 1996-2013 Nebraska NA NA NA NA NA NA 1991-2013 Nevada NA NA NA NA NA NA 1991-2013 New Mexico NA NA NA NA NA NA 1996-2013

312

SEPARATION OF CO2 FROM FLUE GASES BY CARBON-MULTIWALL CARBON NANOTUBE MEMBRANES  

SciTech Connect (OSTI)

Multiwalled carbon nanotubes (MWNT) were found to be an effective separation media for removing CO{sub 2} from N{sub 2}. The separation mechanism favors the selective condensation of CO{sub 2} from the flowing gas stream. Significant uptakes of CO{sub 2} were measured at 30 C and 150 C over the pressure range 0.5 to 5 bar. No measurable uptake of nitrogen was found for this range of conditions. The mass uptake of CO{sub 2} by MWNT was found to increase with increasing temperature. A packed bed of MWNT completely removed CO{sub 2} from a flowing stream of CO{sub 2}/N{sub 2}, and exhibited rapid uptake kinetics for CO{sub 2}.

Rodney Andrews

2001-03-01T23:59:59.000Z

313

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

68,747 68,747 34,577 0.39 0 0.00 34 1.16 14,941 0.29 0 0.00 11,506 0.36 61,058 0.31 I d a h o Idaho 60. Summary Statistics for Natural Gas Idaho, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation.......................... 0 0 0 0 0 Vented

314

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

0 0 0 0.00 0 0.00 0 0.00 540 0.01 0 0.00 2,132 0.07 2,672 0.01 H a w a i i Hawaii 59. Summary Statistics for Natural Gas Hawaii, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation.......................... 0 0 0 0 0 Vented and Flared

315

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

483,052 483,052 136,722 1.54 6,006 0.03 88 3.00 16,293 0.31 283,557 10.38 41,810 1.32 478,471 2.39 F l o r i d a Florida 57. Summary Statistics for Natural Gas Florida, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 47 50 98 92 96 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 7,584 8,011 8,468 7,133 6,706 Total.............................................................. 7,584 8,011 8,468 7,133 6,706 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ...............

316

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

291,898 291,898 113,995 1.29 0 0.00 4 0.14 88,078 1.68 3,491 0.13 54,571 1.73 260,140 1.30 I o w a Iowa 63. Summary Statistics for Natural Gas Iowa, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation.......................... 0 0 0

317

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

29,693 29,693 0 0.00 0 0.00 6 0.20 17,290 0.33 0 0.00 16,347 0.52 33,644 0.17 District of Columbia District of Columbia 56. Summary Statistics for Natural Gas District of Columbia, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation..........................

318

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

42,980 42,980 14,164 0.16 0 0.00 1 0.03 9,791 0.19 23,370 0.86 6,694 0.21 54,020 0.27 D e l a w a r e Delaware 55. Summary Statistics for Natural Gas Delaware, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation..........................

319

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

21,547 21,547 4,916 0.06 0 0.00 0 0.00 7,012 0.13 3 0.00 7,099 0.22 19,031 0.10 N e w H a m p s h i r e New Hampshire 77. Summary Statistics for Natural Gas New Hampshire, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation..........................

320

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

139,881 139,881 26,979 0.30 463 0.00 115 3.92 27,709 0.53 19,248 0.70 28,987 0.92 103,037 0.52 A r i z o n a Arizona 50. Summary Statistics for Natural Gas Arizona, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... NA NA NA NA NA Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 6 6 6 7 7 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 721 508 711 470 417 From Oil Wells ........................................... 72 110 48 88 47 Total.............................................................. 794 618 759 558 464 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

Middle Middle Atlantic Middle Atlantic 37. Summary Statistics for Natural Gas Middle Atlantic, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 1,857 1,981 2,042 1,679 1,928 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 36,906 36,857 26,180 37,159 38,000 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 161,372 152,717 140,444 128,677 152,494 From Oil Wells ........................................... 824 610 539 723 641 Total.............................................................. 162,196 153,327 140,982 129,400 153,134 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed

322

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

386,690 386,690 102,471 1.16 0 0.00 43 1.47 142,319 2.72 5,301 0.19 98,537 3.12 348,671 1.74 M i n n e s o t a Minnesota 71. Summary Statistics for Natural Gas Minnesota, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation..........................

323

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

1,108,583 1,108,583 322,275 3.63 298 0.00 32 1.09 538,749 10.28 25,863 0.95 218,054 6.90 1,104,972 5.52 I l l i n o i s Illinois 61. Summary Statistics for Natural Gas Illinois, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... NA NA NA NA NA Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 382 385 390 372 370 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 337 330 323 325 289 From Oil Wells ........................................... 10 10 10 10 9 Total.............................................................. 347 340 333 335 298 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ...............

324

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

286,485 286,485 71,533 0.81 25 0.00 31 1.06 137,225 2.62 5,223 0.19 72,802 2.31 286,814 1.43 M i s s o u r i Missouri 73. Summary Statistics for Natural Gas Missouri, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... NA NA NA NA NA Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 5 8 12 15 24 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 27 14 8 16 25 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 27 14 8 16 25 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation..........................

325

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

411,951 411,951 100,015 1.13 0 0.00 5 0.17 114,365 2.18 45,037 1.65 96,187 3.05 355,609 1.78 Massachusetts Massachusetts 69. Summary Statistics for Natural Gas Massachusetts, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation..........................

326

Natural Gas  

Gasoline and Diesel Fuel Update (EIA)

226,798 226,798 104,124 1.17 0 0.00 0 0.00 58,812 1.12 2,381 0.09 40,467 1.28 205,783 1.03 North Carolina North Carolina 81. Summary Statistics for Natural Gas North Carolina, 1992-1996 Table 1992 1993 1994 1995 1996 Reserves (billion cubic feet) Estimated Proved Reserves (dry) as of December 31 ....................................... 0 0 0 0 0 Number of Gas and Gas Condensate Wells Producing at End of Year.............................. 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells ......................................... 0 0 0 0 0 From Oil Wells ........................................... 0 0 0 0 0 Total.............................................................. 0 0 0 0 0 Repressuring ................................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ............... 0 0 0 0 0 Wet After Lease Separation..........................

327

Technologies for Boron Removal  

Science Journals Connector (OSTI)

Tests were performed to examine the removal of boron from aqueous solution either with polyvinyl alcohol (PVA) alone or by both PVA and other inorganic additives under room temperature. ... Added calcium hydroxide increased the co-removal of borate with PVA, and this offers a polishing treatment after borate removal by liming. ... As boron removal can be achieved by chemical precipitation and coagulation, it is logical to assume that the EC could remove boron from water and industrial effluent. ...

Yonglan Xu; Jia-Qian Jiang

2007-11-23T23:59:59.000Z

328

Capture of CO2 from flue gas by vacuum pressure swing adsorption using activated carbon beads  

Science Journals Connector (OSTI)

Vacuum pressure swing adsorption (VPSA) for CO2 capture has attracted much research effort with the...2...adsorbent materials. In this work, a new adsorbent, that is, pitch-based activated carbon bead (AC bead), ...

Chunzhi Shen; Jianguo Yu; Ping Li; Carlos A. Grande; Alirio E. Rodrigues

2011-02-01T23:59:59.000Z

329

The utilization of flue gas desulfurization waste by-products in construction brick.  

E-Print Network [OSTI]

??Millions of tons of waste by-products from Texas coal burning plants are produced each year. Two common byproducts are the fuel ashes and calcium sulfate… (more)

Berryman, Charles Wayne

2012-01-01T23:59:59.000Z

330

Application of holographic neural networks for flue gas emissions prediction in the Burnaby incinerator  

SciTech Connect (OSTI)

This article describes the development of a parametric prediction system (PPS) for various emission species at the Burnaby incinerator. The continuous emissions monitoring system at the Burnaby incinerator is shared between three boilers and therefore actual results are only available 5 minutes out of every 15 minutes. The PPS was developed to fill in data for the 10 minutes when the Continuous Emission Monitor (CEM) is measuring the other boilers. It bases its prediction on the last few actual readings taken and parametrically predicts CO, SO2 and NOx. The Burnaby Incinerator is located in the commercial/industrial area of South Burnaby, British Columbia. It consists of three separate lines, each burning ten tonnes of garbage per hour and producing about three tonnes of steam for every tonne of garbage burned. The air pollution control system first cools the combustion products with water injection and then scrubs them with very fine hydrated lime. Carbon is added to the lime to enhance the scrubbing of the combustion products. The CEM monitors the levels of oxygen, carbon monoxide, nitrogen oxides, sulphur dioxide and opacity. In 1996, an expert system was installed on one of boilers at the Burnaby Incinerator plant to determine if it could improve the plant=s operations and reduce overall emission. As part of the expert system, the PPS was developed. Holographic Neural Technology (HNeT), developed by AND Corporation of Toronto, Ontario, is a novel neural network technology using complex numbers in its architecture. Compared to the traditional neural networks, HNeT has some significant advantage. It is more resilient against converging on local minima; is faster training and executing; less prone to over fitting; and, in most cases, has significantly lower error. Selection of independent variabs, training set preparation, testing neural nets and other related issue will be discussed.

Zheng, L.; Dockrill, P.; Clements, B. [Natural Resources Canada, Nepean, Ontario (Canada). CANMET Energy Technology Centre

1997-12-31T23:59:59.000Z

331

Management of dry flue gas desulfurization by-products in underground mines  

SciTech Connect (OSTI)

Disposal of coal combustion by-products (CCBs) in an environmentally sound manner is a major issue facing the coal and utility industries in the US today. Disposal into abandoned sections of underground coal mines may overcome many of the surface disposal problems along with added benefits such as mitigation of subsidence and acid mine drainage. However, many of the abandoned underground coal mines are located far from power plants, requiring long distance hauling of by-products which will significantly contribute to the cost of disposal. For underground disposal to be economically competitive, the transportation and handling cost must be minimized. This requires careful selection of the system and optimal design for efficient operation. The materials handling and system economics research addresses these issues. Transportation and handling technologies for CCBs were investigated from technical, environmental and economic points of view. Five technologies were found promising: (1) Pneumatic Trucks, (2) Pressure Differential Rail Cars, (3) Collapsible Intermodal Containers, (4) Cylindrical Intermodal Tanks, and (5) Coal Hopper Cars with Automatic Retractable Tarping. The first two technologies are currently being utilized in transporting by-products from power plants to disposal sites, whereas the next three are either in development or in conceptualization phases. In this research project, engineering design and cost models were developed for the first four technologies. The engineering design models are in the form of spreadsheets and serve the purpose of determining efficient operating schedules and sizing of system components.

Sevim, H.

1997-06-01T23:59:59.000Z

332

Partially sulfated lime-fly ash sorbents activated by water or steam for SO{sub 2} removal at a medium temperature  

SciTech Connect (OSTI)

Laboratory experiments were conducted to investigate the reactivity of partially sulfated lime-fly ash sorbents activated by water or steam for SO{sub 2} removal. Sulfation tests were performed at 550{sup o}C using a fixed bed reactor under conditions simulating economizer zone injection flue gas desulfurization. Activation experiments were conducted with water or steam using a range of temperatures between 100 and 550{sup o}C. The results showed that the reactivity of the sorbents was closely related to the content of Ca(OH){sub 2} formed in the activation process, which varied with the water or steam temperature. The sulfur dioxide capture capacity of Ca(OH){sub 2} in the sorbent is higher than that of CaO at a medium temperature. Water or steam temperatures in the range of 100-200{sup o}C are favorable to the formation of Ca(OH){sub 2} from CaO. 15 refs., 8 figs., 2 tabs.

Liming Shi; Xuchang Xu [Tsinghua University, Beijing (China). Department of Thermal Engineering

2005-12-01T23:59:59.000Z

333

Turbomachinery debris remover  

DOE Patents [OSTI]

An apparatus for removing debris from a turbomachine. The apparatus includes housing and remotely operable viewing and grappling mechanisms for the purpose of locating and removing debris lodged between adjacent blades in a turbomachine.

Krawiec, Donald F. (Pittsburgh, PA); Kraf, Robert J. (North Huntingdon, PA); Houser, Robert J. (Monroeville, PA)

1988-01-01T23:59:59.000Z

334

Virginia Natural Gas Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0

335

Methods for reducing emissions of dioxins and furans in flue gases at plants burning solid domestic waste  

Science Journals Connector (OSTI)

Methods are discussed for reducing emissions of toxic chlorinated dibenzo-dioxins and dibenzo-furans in flue gases at plants which burn solid domestic waste. Results are presented from a study of ... number of th...

A. N. Tugov; V. F. Moskvichev; L. G. Fedorov…

2009-01-01T23:59:59.000Z

336

Natural Gas Industrial Price  

Gasoline and Diesel Fuel Update (EIA)

Citygate Price Residential Price Commercial Price Industrial Price Electric Power Price Gross Withdrawals Gross Withdrawals From Gas Wells Gross Withdrawals From Oil Wells Gross Withdrawals From Shale Gas Wells Gross Withdrawals From Coalbed Wells Repressuring Nonhydrocarbon Gases Removed Vented and Flared Marketed Production NGPL Production, Gaseous Equivalent Dry Production Imports By Pipeline LNG Imports Exports Exports By Pipeline LNG Exports Underground Storage Capacity Gas in Underground Storage Base Gas in Underground Storage Working Gas in Underground Storage Underground Storage Injections Underground Storage Withdrawals Underground Storage Net Withdrawals Total Consumption Lease and Plant Fuel Consumption Pipeline & Distribution Use Delivered to Consumers Residential Commercial Industrial Vehicle Fuel Electric Power Period: Monthly Annual

337

E-Print Network 3.0 - atmospheric methane removal Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

from the U-trap, remove carbon and hydrogen impurities, oxidize the purified methane to CO2 and H2... . The helium gas was recycled through the U-trap (1) to remove and purify...

338

Method and system for the removal of oxides of nitrogen and sulfur from combustion processes  

DOE Patents [OSTI]

A process for removing oxide contaminants from combustion gas, and employing a solid electrolyte reactor, includes: (a) flowing the combustion gas into a zone containing a solid electrolyte and applying a voltage and at elevated temperature to thereby separate oxygen via the solid electrolyte, (b) removing oxygen from that zone in a first stream and removing hot effluent gas from that zone in a second stream, the effluent gas containing contaminant, (c) and pre-heating the combustion gas flowing to that zone by passing it in heat exchange relation with the hot effluent gas.

Walsh, John V. (Glendora, CA)

1987-12-15T23:59:59.000Z

339

Risk Removal | Department of Energy  

Energy Savers [EERE]

Risk Removal Risk Removal Workers safely remove old mercury tanks from the Y-12 National Security Complex. Workers safely remove old mercury tanks from the Y-12 National Security...

340

Ammonia synthesis gas purification  

SciTech Connect (OSTI)

This patent describes the purification of a reformed gas mixture following water gas shift conversion to produce a purified ammonia synthesis gas stream. The improved processing sequence consisting essentially of: (A) Selectively catalytically oxidizing the residual carbon monoxide content of the gas mixture to carbon dioxide so as to reduce the carbon monoxide content of the gas mixture to less than about 20 ppm, the selective catalytic oxidation being carried out with an excess of air, with the excess oxygen being catalytically reacted with a small amount of hydrogen so that the residual oxygen level is reduced to less than about 3 ppm; (B) removing the bulk of the carbon dioxide content of the gas mixture by liquid absorption; (C) Removing residual amounts of carbon monoxide, carbon dioxide and water by selective adsorption on the fixed beds of a thermal swing adsorption system, a dry, purified ammonia ammonia synthesis gas stream containing less than a total of 10 ppm of carbon monoxide and carbon dioxide being recovered from the thermal swing adsorption system; (D) Passing the resulting dry, purified ammonia synthesis gas stream having a low content of methane to an ammonia production operation without intermediate passage of the ammonia synthesis gas stream to a methanation unit or to a cryogenic unit for removal of carbon monoxide and carbon dioxide therefrom; whereby the efficiency of the overall purification operation and the effective utilization of hydrogen are enhanced.

Fuderer, A.

1986-02-25T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

Energy consumption analysis for CO2 separation from gas mixtures  

Science Journals Connector (OSTI)

Abstract CO2 separation is an energy intensive process, which plays an important role in both energy saving and CO2 capture and storage (CCS) implementation to deal with global warming. To quantitatively investigate the energy consumption of CO2 separation from different CO2 streams and analyze the effect of temperature, pressure and composition on energy consumption, in this work, the theoretical energy consumption of CO2 separation from flue gas, lime kiln gas, biogas and bio-syngas was calculated. The results show that the energy consumption of CO2 separation from flue gas is the highest and that from biogas is the lowest, and the concentration of CO2 is the most important factor affecting the energy consumption when the CO2 concentration is lower than 0.15 in mole fraction. Furthermore, if the CO2 captured from flue gases in CCS was replaced with that from biogases, i.e. bio-CO2, the energy saving would be equivalent to 7.31 million ton standard coal for China and 28.13 million ton standard coal globally, which corresponds to 0.30 billion US$ that can be saved for China and 1.36 billion US$ saved globally. This observation reveals the importance of trading fossil fuel-based CO2 with bio-CO2.

Yingying Zhang; Xiaoyan Ji; Xiaohua Lu

2014-01-01T23:59:59.000Z

342

Chapter 10 - Natural Gas Sweetening  

Science Journals Connector (OSTI)

Abstract Acid gas constituents present in most natural gas streams are mainly hydrogen sulfide (H2S) and carbon dioxide (CO2). Many gas streams, however, particularly those in a refinery or manufactured gases, may contain mercaptans, carbon sulfide, or carbonyl sulfide. The level of acid gas concentration in the sour gas is an important consideration for selecting the proper sweetening process. Some processes are applicable for removal of large quantities of acid gas, and other processes have the capacity for removing acid gas constituents to ppm range. This chapter covers the minimum process requirements, criteria, and features for accomplishment of process design of gas sweetening units. The basic principles for process design of main equipment, piping, and instrumentation together with guidelines on present developments and process selection in the gas sweetening process are the main objectives throughout this chapter.

Alireza Bahadori

2014-01-01T23:59:59.000Z

343

Radiator debris removing apparatus and work machine using same  

DOE Patents [OSTI]

A radiator assembly includes a finned radiator core and a debris removing apparatus having a compressed air inlet and at least one compressed air outlet configured to direct compressed air through the radiator core. A work machine such as a wheel loader includes a radiator and a debris removing apparatus coupled with on-board compressed air and having at least one pressurized gas outlet configured to direct a gas toward the face of the radiator.

Martin, Kevin L. (Washburn, IL); Elliott, Dwight E. (Chillicothe, IL)

2008-09-02T23:59:59.000Z

344

Silica Scaling Removal Process  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Silica Scaling Removal Process Silica Scaling Removal Process Silica Scaling Removal Process Scientists at Los Alamos National Laboratory have developed a novel technology to remove both dissolved and colloidal silica using small gel particles. Available for thumbnail of Feynman Center (505) 665-9090 Email Silica Scaling Removal Process Applications: Cooling tower systems Water treatment systems Water evaporation systems Potential mining applications (produced water) Industry applications for which silica scaling must be prevented Benefits: Reduces scaling in cooling towers by up to 50% Increases the number of cycles of concentration substantially Reduces the amount of antiscaling chemical additives needed Decreases the amount of makeup water and subsequent discharged water (blowdown) Enables considerable cost savings derived from reductions in

345

Alternative CO2 Removal Solutions for the LNG Process on an FPSO.  

E-Print Network [OSTI]

?? The Höegh LNG FPSO is designed for a CO2 removal of a gas stream containing 12.3% CO, but has a desire to add discuss… (more)

Haugen, Erlend Lunde

2011-01-01T23:59:59.000Z

346

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

1 1 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

347

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

9 9 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

348

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

9 9 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

349

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

1 1 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 7,279 6,446 3,785 3,474 3,525 Total................................................................... 7,279 6,446 3,785 3,474 3,525 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 7,279 6,446 3,785 3,474 3,525 Nonhydrocarbon Gases Removed ..................... 788 736 431

350

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 9 8 7 9 6 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 368 305 300 443 331 From Oil Wells.................................................. 1 1 0 0 0 Total................................................................... 368 307 301 443 331 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 368 307 301 443 331 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

351

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 98 96 106 109 111 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 869 886 904 1,187 1,229 From Oil Wells.................................................. 349 322 288 279 269 Total................................................................... 1,218 1,208 1,193 1,466 1,499 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 5 12 23 Wet After Lease Separation................................ 1,218 1,208 1,188 1,454 1,476 Nonhydrocarbon Gases Removed .....................

352

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

9 9 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 4 4 4 4 4 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 7 7 6 6 5 Total................................................................... 7 7 6 6 5 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 7 7 6 6 5 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

353

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

3 3 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

354

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

5 5 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

355

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

3 3 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

356

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

3 3 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

357

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

3 3 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

358

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

1 1 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

359

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 380 350 400 430 280 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 1,150 2,000 2,050 1,803 2,100 Total................................................................... 1,150 2,000 2,050 1,803 2,100 Repressuring ...................................................... NA NA NA 0 NA Vented and Flared.............................................. NA NA NA 0 NA Wet After Lease Separation................................ 1,150 2,000 2,050 1,803 2,100 Nonhydrocarbon Gases Removed .....................

360

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

5 5 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

1 1 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 1,502 1,533 1,545 2,291 2,386 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 899 1,064 1,309 1,464 3,401 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 899 1,064 1,309 1,464 3,401 Repressuring ...................................................... NA NA NA 0 NA Vented and Flared.............................................. NA NA NA 0 NA Wet After Lease Separation................................ 899 1,064 1,309 1,464 3,401 Nonhydrocarbon Gases Removed .....................

362

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

9 9 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

363

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

3 3 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

364

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

365

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

3 3 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 7 7 5 7 7 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 34 32 22 48 34 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 34 32 22 48 34 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 34 32 22 48 34 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

366

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

1 1 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

367

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

1 1 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ......................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells...................................................... 0 0 0 0 0 From Oil Wells........................................................ 0 0 0 0 0 Total......................................................................... 0 0 0 0 0 Repressuring ............................................................ 0 0 0 0 0 Vented and Flared .................................................... 0 0 0 0 0 Wet After Lease Separation...................................... 0 0 0 0 0 Nonhydrocarbon Gases Removed............................ 0 0 0 0 0 Marketed Production

368

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

369

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

3 3 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

370

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 17 20 18 15 15 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 1,412 1,112 837 731 467 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 1,412 1,112 837 731 467 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 1,412 1,112 837 731 467 Nonhydrocarbon Gases Removed ..................... 198 3 0 0 0 Marketed Production

371

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 0 0 0 0 0 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 0 0 0 0 0 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 0 0 0 0 0 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 0 0 0 0 0 Nonhydrocarbon Gases Removed ..................... 0 0 0 0 0 Marketed Production ..........................................

372

Physics and chemistry of E-beam stack gas processing. Final report, 20 September 1982-14 January 1984  

SciTech Connect (OSTI)

The purpose of this program is to investigate some of the basic physics and chemistry of the electron beam induced NO/sub x/ and SO/sub x/ removal process. The program involves both kinetic modelling and diagnostic development. The development of an adequate kinetic model is necessary in order to scale the laboratory results, which are currently available, to process conditions closer to those that will be encountered at full scale operation. It is also necessary in order to place the laboratory data on a firm theoretical foundation. The development of real time optical diagnostics is a necessary supporting task for these goals in order to obtain kinetic data on some of the myriad of species that are present in this hostile environment (X-rays present; hot, acidic gas) which is difficult to access by conventional methods. This particular NO/sub x//SO/sub x/ removal process involves the irradiation of combustion products t temperatures around 100/sup 0/C with a beam of high energy electrons. The current study expands upon the mechanistic studies. A detailed kinetic model is described which includes all the necessary assumptions that enter in order to take the very large number of possible processes that occur in e-beam irradiated mixtures and reduce them to some tractable number. Quantitative comparisons are then made between the kinetic model and experimental data. Another phase of this program is the development of laser diagnostics to probe various species in the irradiated flue gas. The experimental phase of program is first described including a discussion of our e-beam facility and the methods used to accurately measure energy deposition. A description of the laser diagnostics follows. 37 references, 22 figures, 7 tables.

Slater, R.

1983-10-01T23:59:59.000Z

373

Enhanced membrane gas separations  

SciTech Connect (OSTI)

An improved membrane gas separation process is described comprising: (a) passing a feed gas stream to the non-permeate side of a membrane system adapted for the passage of purge gas on the permeate side thereof, and for the passage of the feed gas stream in a counter current flow pattern relative to the flow of purge gas on the permeate side thereof, said membrane system being capable of selectively permeating a fast permeating component from said feed gas, at a feed gas pressure at or above atmospheric pressure; (b) passing purge gas to the permeate side of the membrane system in counter current flow to the flow of said feed gas stream in order to facilitate carrying away of said fast permeating component from the surface of the membrane and maintaining the driving force for removal of the fast permeating component through the membrane from the feed gas stream, said permeate side of the membrane being maintained at a subatmospheric pressure within the range of from about 0.1 to about 5 psia by vacuum pump means; (c) recovering a product gas stream from the non-permeate side of the membrane; and (d) discharging purge gas and the fast permeating component that has permeated the membrane from the permeate side of the membrane, whereby the vacuum conditions maintained on the permeate side of the membrane by said vacuum pump means enhance the efficiency of the gas separation operation, thereby reducing the overall energy requirements thereof.

Prasad, R.

1993-07-13T23:59:59.000Z

374

Process for removing an organic compound from water  

DOE Patents [OSTI]

A process for removing organic compounds from water is disclosed. The process involves gas stripping followed by membrane separation treatment of the stripping gas. The stripping step can be carried out using one or multiple gas strippers and using air or any other gas as stripping gas. The membrane separation step can be carried out using a single-stage membrane unit or a multistage unit. Apparatus for carrying out the process is also disclosed. The process is particularly suited for treatment of contaminated groundwater or industrial wastewater.

Baker, Richard W. (Palo Alto, CA); Kaschemekat, Jurgen (Palo Alto, CA); Wijmans, Johannes G. (Menlo Park, CA); Kamaruddin, Henky D. (San Francisco, CA)

1993-12-28T23:59:59.000Z

375

Warm Gas Cleanup  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Warm Gas Cleanup Warm Gas Cleanup NETL Office of Research and Development Project Number: FWP-2012.03.03 Task 5 Project Description The Environmental Protection Agency (EPA) has established strict regulations for the trace contaminant emissions from integrated gasification combined cycle (IGCC) systems. The Department of Energy (DOE) performance goals for trace contaminant removal were selected to meet or exceed EPA's standard limits for contaminants, as well as to avoid poisoning of: the catalysts utilized in making liquids from fuel gas the electrodes in fuel cells selective catalytic reduction (SCR) catalysts The objective of the NETL's ORD Warm Gas Cleanup project is to assist in achieving both DOE and EPA targets for trace contaminant capture from coal gasification, while preserving the high thermal efficiency of the IGCC system. To achieve this, both lab and pilot-scale research is underway to develop sorbents capable of removing the following contaminants from high temperature syngas (up to 550°F):

376

Evaluation of gas-liquid separation performance of natural gas filters  

Science Journals Connector (OSTI)

Fibrous filters are often used to remove contaminants including both dusts and liquid droplets from natural gas. This paper aims to evaluate the gas-liquid separation performance of three types of cartridge filte...

Baisong Li; Zhongli Ji; Xue Yang

2009-12-01T23:59:59.000Z

377

Post-combustion Carbon Capture with a Gas Separation Membrane: Parametric Study, Capture Cost, and Exergy Analysis  

Science Journals Connector (OSTI)

Post-combustion Carbon Capture with a Gas Separation Membrane: Parametric Study, Capture Cost, and Exergy Analysis ... (5) In a post-combustion CO2 capture process, the purity of the captured CO2 in the permeate stream mainly depends upon the selectivity of CO2 over the other gas species, such as N2 and O2. ... Capturing CO2 from flue gases in a power plant is not like traditional gas processing or purification, there are no strict requirements on the decarbonized sweet gas, which means no strict requirement on the CO2 concentration in the sweet gas or CO2 capture ratio. ...

Xiangping Zhang; Xuezhong He; Truls Gundersen

2013-03-04T23:59:59.000Z

378

Drum lid removal tool  

DOE Patents [OSTI]

A tool for removing the lid of a metal drum wherein the lid is clamped over the drum rim without protruding edges, the tool having an elongated handle with a blade carried by an angularly positioned holder affixed to the midsection of the handle, the blade being of selected width to slice between lid lip and the drum rim and, when the blade is so positioned, upward motion of the blade handle will cause the blade to pry the lip from the rim and allow the lid to be removed.

Pella, Bernard M. (Martinez, GA); Smith, Philip D. (North Augusta, SC)

2010-08-24T23:59:59.000Z

379

Water-saving liquid-gas conditioning system  

DOE Patents [OSTI]

A method for treating a process gas with a liquid comprises contacting a process gas with a hygroscopic working fluid in order to remove a constituent from the process gas. A system for treating a process gas with a liquid comprises a hygroscopic working fluid comprising a component adapted to absorb or react with a constituent of a process gas, and a liquid-gas contactor for contacting the working fluid and the process gas, wherein the constituent is removed from the process gas within the liquid-gas contactor.

Martin, Christopher; Zhuang, Ye

2014-01-14T23:59:59.000Z

380

Chapter 6 - Dehydration of Natural Gas  

Science Journals Connector (OSTI)

Publisher Summary This chapter reviews several methods used for dehydrating natural gas. Dehydration is the process by which water is removed from natural gas. This is a common method used for preventing hydrate formation. There are other reasons for dehydrating natural gas. Removing water vapor reduces the risk of corrosion in transmission lines. Furthermore, dehydration improves the efficiency of pipelines by reducing the amount of liquid accumulating in the lines—or even eliminates it completely. There are several methods of dehydrating natural gas. The most common of these are: glycol dehydration (liquid desiccant), molecular sieves (solid adsorbent), and refrigeration. The most common method for dehydration in the natural gas industry is the use of a liquid desiccant contactor-regeneration process. In this process, the wet gas is contacted with a lean solvent. The lean solvent, producing a rich solvent stream and a dry gas, absorbs the water in the gas. Unlike glycol dehydration, which is an absorption process, dehydration with molecular sieves is an adsorption process. Water in the gas adheres to the solid phase (the solid being the mole sieve), and thus is removed from the natural gas. Molecular sieves are usually used when very dry gas is required. The usual purpose of a refrigeration plant is to remove heavy hydrocarbons from a natural gas stream—to make hydrocarbon dewpoint specification—but this process also removes water.

John J. Carroll

2003-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

Condensate removal device  

DOE Patents [OSTI]

A condensate removal device is disclosed which incorporates a strainer in unit with an orifice. The strainer is cylindrical with its longitudinal axis transverse to that of the vapor conduit in which it is mounted. The orifice is positioned inside the strainer proximate the end which is remoter from the vapor conduit.

Maddox, James W. (Newport News, VA); Berger, David D. (Alexandria, VA)

1984-01-01T23:59:59.000Z

382

NO, Reduction in a Gas Fired Utility Boiler by Combustion Modifications  

E-Print Network [OSTI]

Data on the effect of several combustion modifications on the for-math of nitrogen oxides and on boiler efficiency were acquired and analyzed for a 110 MW gas fired utility boiler. The results from the study showed that decreasing the oxygen in the flue gas from 2.2% to 0.6 % reduced the NO, formation by 33 % and also gave better boiler efficiencies. Flue gas recirculation through the bottom of the fire4mx WBS founb to be Ineffective. Staged combustion was found to reduce the NO, emlssions by as much as 55 % while decreasing the efficiency by about 5%. Adjustment of the burner air registers reduced the NO, formation by about 20 ppm. The lowest NO, emisdons of 42 ppm (at about 3 % 02) in the stack was obtained for air only to one top burner and 0.5 % oxygen in the flue gas. The reduction of nitrogen oxides (NO,) emissions from steam boilers has been under study for several years. The NO, from boilers consist almost entirely of nitric oxide (NO) and nitrogen dioxide (N02) with NO2 usually only l or 2 % of the total. After leaving the stack, the NO eventually combines with atmospheric oxygen to form NOp. The Environmental Protection Agency has sponsored several studies1-I0 on reducing NO, emissions while maintaining thermal efficiency of boilers. Other studies have been sponsored by The Electric Power Research Institute (EPRI) " and Argonne National

Jerry A. Bullin; Dan Wilkerson

1982-01-01T23:59:59.000Z

383

New packing in absorption systems for trapping benzene from coke-oven gas  

SciTech Connect (OSTI)

The efficiency of benzene removal from coke-oven gas in absorption units OAO Alchevskkoks with new packing is assessed.

V.V. Grabko; V.M. Li; T.A. Shevchenko; M.A. Solov'ev [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

384

Cement kiln flue dust as a source of lime and potassium in four East Texas soils  

E-Print Network [OSTI]

the blight encountered the previous year. Forage sorghum (DeKalb SX-11) was planted 5/1/73, 4/26/74 and, 6/9/75) . Yield of corn grain, corn forage, and sorghum forage were determined for the three growing seasons. Leaf samples were also taken... by rate and source of lime, de th, and time. Treatment k /ha 0 mo. 3 mo. 8 mo. 11 mo. 17 mo. 0 to 15 cm depth 8000 flue dust 2000 5QQ II II S. 6 a s. s a 5. 6 a 6. 9 c 6. 1 ab 5. 7 a 7. 2 c 6. 5 bc 5. 9 ab 6. 5 bc 7. 0 c 6. 0 abc 6. 4 b 5. 6 a...

Poole, Warren David

2012-06-07T23:59:59.000Z

385

Exhaust gas clean up process  

DOE Patents [OSTI]

A method of cleaning an exhaust gas containing particulates, SO.sub.2 and NO.sub.x includes prescrubbing with water to remove HCl and most of the particulates, scrubbing with an aqueous absorbent containing a metal chelate and dissolved sulfite salt to remove NO.sub.x and SO.sub.2, and regenerating the absorbent solution by controlled heating, electrodialysis and carbonate salt addition. The NO.sub.x is removed as N.sub.2 or nitrogen-sulfonate ions and the oxides of sulfur are removed as a vaulable sulfate salt.

Walker, Richard J. (McMurray, PA)

1989-01-01T23:59:59.000Z

386

DOE Removes Brookhaven Contractor  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

DOE Removes DOE Removes Brookhaven Contractor Peña sends a message to DOE facilities nationwide INSIDE 2 Accelerator Rx 4 FermiKids 6 Spring at Fermilab Photos courtesy of Brookhaven National Laboratory by Judy Jackson, Office of Public Affairs Secretary of Energy Federico Peña announced on Thursday, May 1, that the Department of Energy would immediately terminate the current management contract with Associated Universities, Inc. at Brookhaven National Laboratory in Upton, New York. Peña said that he made the decision after receiving the results of a laboratory safety management review conducted by the independent oversight arm of DOE's Office of Environment, Safety and Health. In addition, the Secretary said he found unacceptable "the continued on page 8 Volume 20 Friday, May 16, 1997

387

Pneumatic soil removal tool  

DOE Patents [OSTI]

A soil removal tool is provided for removing radioactive soil, rock and other debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder mounted on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably mounted on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator valve mounted on the handle, to provide movement of the movable jaw. 3 figs.

Neuhaus, J.E.

1992-10-13T23:59:59.000Z

388

Mercury and tritium removal from DOE waste oils  

SciTech Connect (OSTI)

This work covers the investigation of vacuum extraction as a means to remove tritiated contamination as well as the removal via sorption of dissolved mercury from contaminated oils. The radiation damage in oils from tritium causes production of hydrogen, methane, and low-molecular-weight hydrocarbons. When tritium gas is present in the oil, the tritium atom is incorporated into the formed hydrocarbons. The transformer industry measures gas content/composition of transformer oils as a diagnostic tool for the transformers` condition. The analytical approach (ASTM D3612-90) used for these measurements is vacuum extraction of all gases (H{sub 2}, N{sub 2}, O{sub 2}, CO, CO{sub 2}, etc.) followed by analysis of the evolved gas mixture. This extraction method will be adapted to remove dissolved gases (including tritium) from the SRS vacuum pump oil. It may be necessary to heat (60{degrees}C to 70{degrees}C) the oil during vacuum extraction to remove tritiated water. A method described in the procedures is a stripper column extraction, in which a carrier gas (argon) is used to remove dissolved gases from oil that is dispersed on high surface area beads. This method appears promising for scale-up as a treatment process, and a modified process is also being used as a dewatering technique by SD Myers, Inc. (a transformer consulting company) for transformers in the field by a mobile unit. Although some mercury may be removed during the vacuum extraction, the most common technique for removing mercury from oil is by using sulfur-impregnated activated carbon (SIAC). SIAC is currently being used by the petroleum industry to remove mercury from hydrocarbon mixtures, but the sorbent has not been previously tested on DOE vacuum oil waste. It is anticipated that a final process will be similar to technologies used by the petroleum industry and is comparable to ion exchange operations in large column-type reactors.

Klasson, E.T. [Oak Ridge National Lab., TN (United States)

1997-10-01T23:59:59.000Z

389

Combining steam-methane reforming, water-gas shift, and CO{sub 2} removal in a single-step process for hydrogen production. Final report for period March 15, 1997 - December 14, 2000  

SciTech Connect (OSTI)

The objective of the research project was to determine the feasibility of a simpler, more energy-efficient process for the production of 95+% H{sub 2} from natural gas, and to collect sufficient experimental data on the effect of reaction parameters to guide additional larger-scale process development. The overall objectives were accomplished. 95+% H{sub 2} was produced in a single reaction step by adding a calcium-based CO{sub 2} acceptor to standard Ni-based reforming catalyst. The spent acceptor was successfully regenerated and used in a number of reaction steps with only moderate loss in activity as the number of cycles increased. Sufficient experimental data were collected to guide further larger-scale experimental work designed to investigate the economic feasibility of the process.

Alejandro Lopez Ortiz; Bhaskar Balasubramanian; Douglas P. Harrison

2001-02-01T23:59:59.000Z

390

Comparative Analysis of Alternative Means for Removing Noncondensable Gases  

Open Energy Info (EERE)

Comparative Analysis of Alternative Means for Removing Noncondensable Gases Comparative Analysis of Alternative Means for Removing Noncondensable Gases from Flashed-Steam Geothermal Power Plants:April 1999 - March 2000 Dataset Summary Description This dataset corresponds to the final report on a screening study to compare six methods of removing noncondensable gases from direct-use geo-thermal steam power plants. This report defines the study methodologies and compares the performance and economics of selected gas-removal systems. Recommendations are presented for follow-up investigations and implementation of some of the technologies discussed. The specific gas-removal methods include five vacuum system configurations using the conventional approach of evacuating gas/vapor mixtures from the power plant condenser system and a system for physical separation of steam and gases upstream of the power turbine. The study focused on flashed-steam applications, but the results apply equally well to flashed-steam and dry-steam geothermal power plant configurations. Two gas-removal options appear to offer profitable economic potential. The hybrid vacuum system configurations and the reboiler process yield positive net present value results over wide-ranging gas concentrations. The hybrid options look favorable for both low-temperature and high-temperature resource applications. The reboiler looks profitable for low-temperature resource applications for gas levels above about 20,000 parts per million by volume. A vacuum system configuration using a three-stage turbocompressor battery may be profitable for low-temperature resources, but results show that the hybrid system is more profitable. The biphase eductor alternative cannot be recommended for commercialization at this time. The report is available from NREL's publication database.

391

Novel Electrochemical CO2 Removal Technology For Combustion of Fossil-Fuels  

SciTech Connect (OSTI)

Electrochemical gas separation concepts are often neglected when discussing options to manage CO2 emissions. Electrochemical approaches are selective and do not require periodic regeneration. This paper will review prior work on electrochemical CO2 separation and compare the parasitic energy penalties of this approach to more conventional approaches of capturing CO2 from flue gas streams. A new concept to reduce the electrochemical parasitic energy penalties will be introduced and a preliminary analysis of the concept will be discussed. Relative to a conventional monoethanolamine (MEA) solvent approach, electrochemical CO2 capture does require less energy on a per-mole-of-CO2 basis. However, there are trade-offs since an electrochemical pumping approach requires electrical energy, instead of lower grade thermal energy. Although there are several issues with electrochemical CO2 capture, efforts to reduce parasitic losses of CO2 separation may need to consider such novel alternatives.

Douglas L. Straub; Maria Salazar-Villalpando

2008-07-14T23:59:59.000Z

392

Chapter six - Dehydration of natural gas  

Science Journals Connector (OSTI)

Publisher Summary This chapter describes the dehydration process of natural gas. Dehydration is the process by which water is removed from natural gas. This is a common method used for preventing hydrate formation. If there is no water present, it is impossible for a hydrate to form. If there is only a small amount of water present, the formation of hydrate is less likely. There are other reasons for dehydrating natural gas. The removal of water vapor reduces the risk of corrosion in transmission lines. Furthermore, dehydration improves the efficiency of pipelines by reducing the amount of liquid accumulating in the lines—or even eliminates it completely. There are several methods of dehydrating natural gas. The most common are: glycol dehydration (liquid desiccant), molecular sieves (solid adsorbent), and refrigeration. In glycol dehydration process, the wet gas is contacted with a lean solvent (containing only a small amount of water). The water in the gas is absorbed by the lean solvent, producing a rich solvent stream (one containing more water) and a dry gas. In mole sieves, water in the gas adheres to the solid phase, the solid being the mole sieve, and thus is removed from the natural gas. The usual purpose of a refrigeration plant is to remove heavy hydrocarbons from a natural gas stream—to make hydrocarbon dew point specification. However, this process also removes water.

John J. Carroll

2009-01-01T23:59:59.000Z

393

U.S. crude oil, natural gas, and natural gas liquids reserves 1997 annual report  

SciTech Connect (OSTI)

This report presents estimates of proved reserves of crude oil, natural gas, and natural gas liquids as of December 31, 1997, as well as production volumes for the US and selected States and State subdivisions for the year 1997. Estimates are presented for the following four categories of natural gas: total gas (wet after lease separation), nonassociated gas and associated-dissolved gas (which are the two major types of wet natural gas), and total dry gas (wet gas adjusted for the removal of liquids at natural gas processing plants). In addition, reserve estimates for two types of natural gas liquids, lease condensate and natural gas plant liquids, are presented. Also included is information on indicated additional crude oil reserves and crude oil, natural gas, and lease condensate reserves in nonproducing reservoirs. A discussion of notable oil and gas exploration and development activities during 1997 is provided. 21 figs., 16 tabs.

NONE

1998-12-01T23:59:59.000Z

394

Ordered Vertex Removal Subgraph Problems  

E-Print Network [OSTI]

of the vertex removal and subgraph problems are shown to be P­complete. In addition, a natural lex­ icographicOrdered Vertex Removal and Subgraph Problems Ray Greenlaw Department of Computer Science University­8703196. #12; Vertex Removal and Graph Problems Ray Greenlaw Department of Computer Science FR­35

Greenlaw, Ray

395

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

9 9 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 42,475 42,000 45,000 46,203 47,117 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 264,139 191,889 190,249 187,723 197,217 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 264,139 191,889 190,249 187,723 197,217 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 264,139 191,889 190,249 187,723 197,217 Nonhydrocarbon Gases Removed

396

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

5 5 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 71 68 69 61 61 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 648 563 531 550 531 From Oil Wells.................................................. 10,032 10,751 9,894 11,055 11,238 Total................................................................... 10,680 11,313 10,424 11,605 11,768 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 1,806 2,043 1,880 2,100 2,135 Wet After Lease Separation................................ 8,875 9,271 8,545 9,504 9,633 Nonhydrocarbon Gases Removed

397

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

5 5 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 3,051 3,521 3,429 3,506 3,870 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 71,545 71,543 76,915 R 143,644 152,495 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 71,545 71,543 76,915 R 143,644 152,495 Repressuring ...................................................... NA NA NA 0 NA Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 71,545 71,543 76,915 R 143,644 152,495 Nonhydrocarbon Gases Removed

398

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 5,775 5,913 6,496 5,878 5,781 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 17,741 27,632 36,637 35,943 45,963 From Oil Wells.................................................. 16 155 179 194 87 Total................................................................... 17,757 27,787 36,816 36,137 46,050 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 17,757 27,787 36,816 36,137 46,050 Nonhydrocarbon Gases Removed

399

Number of Gas and Gas Condensate Wells  

Gasoline and Diesel Fuel Update (EIA)

7 7 2000 2001 2002 2003 2004 Number of Gas and Gas Condensate Wells Producing at End of Year ................................... 13,487 14,370 14,367 12,900 13,920 Production (million cubic feet) Gross Withdrawals From Gas Wells................................................ 81,545 81,723 88,259 87,608 94,259 From Oil Wells.................................................. 0 0 0 0 0 Total................................................................... 81,545 81,723 88,259 87,608 94,259 Repressuring ...................................................... 0 0 0 0 0 Vented and Flared.............................................. 0 0 0 0 0 Wet After Lease Separation................................ 81,545 81,723 88,259 87,608 94,259 Nonhydrocarbon Gases Removed

400

Management of dry flue gas desulfurization by-products in underground mines. Quarterly report, August 1--October 31, 1997  

SciTech Connect (OSTI)

The objective of this project was to develop and demonstrate two technologies for the placement of coal combustion by-products in abandoned underground coal mines, and to assess the environmental impact of these technologies for the management of CCB materials. The two technologies for the underground placement that were to be developed and demonstrated are: (1) pneumatic placement using virtually dry CCB products, and (2) hydraulic placement using a paste mixture of CCB products with about 70% solids. The period covered by this report is the second quarter of Phase 3 of the overall program. During this period over 8,000 tons of CCB mixtures was injected using the hydraulic paste technology. This amount of material virtually filled the underground opening around the injection well, and was deemed sufficient to demonstrate fully the hydraulic injection technology. By the end of this quarter about 2,000 tons of fly ash had been placed underground using the pneumatic placement technology. While the rate of injection of about 50 tons per hour met design criteria, problems were experienced in the delivery of fly ash to the pneumatic demonstration site. The source of the fly ash, the Archer Daniels Midland Company power plant at Decatur, Illinois is some distance from the demonstration site, and often sufficient tanker trucks are not available to haul enough fly ash to fully load the injection equipment. Further, on some occasions fly ash from the plant was not available. The injection well was plugged three times during the demonstration. This typically occurred due to cementation of the FBC ash in contact with water. After considerable deliberations and in consultation with the technical project officer, it was decided to stop further injection of CCB`s underground using the developed pneumatic technology.

Chugh, Y.P.

1997-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "removal flue gas" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Geological and Geotechnical Site Investigation for the Design of a CO2 Rich Flue Gas Direct Injection and Storage Facility  

SciTech Connect (OSTI)

With international efforts to limit anthropogenic carbon in the atmosphere, various CO{sub 2} sequestration methods have been studied by various facilities worldwide. Basalt rock in general has been referred to as potential host material for mineral carbonation by various authors, without much regard for compositional variations due to depositional environment, subsequent metamorphism, or hydrothermal alteration. Since mineral carbonation relies on the presence of certain magnesium, calcium, or iron silicates, it is necessary to study the texture, mineralogy, petrology, and geochemistry of specific basalts before implying potential for mineral carbonation. The development of a methodology for the characterization of basalts with respect to their susceptibility for mineral carbonation is proposed to be developed as part of this research. The methodology will be developed based on whole rock data, petrography and microprobe analyses for samples from the Caledonia Mine in Michigan, which is the site for a proposed small-scale demonstration project on mineral carbonation in basalt. Samples from the Keweenaw Peninsula will be used to determine general compositional trends using whole rock data and petrography. Basalts in the Keweenaw Peninsula have been subjected to zeolite and prehnite-pumpellyite facies metamorphism with concurrent native copper deposition. Alteration was likely due to the circulation of CO{sub 2}-rich fluids at slightly elevated temperatures and pressures, which is the process that is attempted to be duplicated by mineral carbonation.

Metz, Paul; Bolz, Patricia

2013-03-25T23:59:59.000Z

402

Flue-Gas Carbon Capture on Carbonaceous Sorbents:? Toward a Low-Cost Multifunctional Carbon Filter for “Green” Energy Producers  

Science Journals Connector (OSTI)

Mr. Ian Andrews and Mr. Nick Rahn (PacifiCorp Energy), Mr. Robert Matius and Mr. Eldon Lindt (Xcel Energy), Mr. George Farthing (Babcock & Wilcox Company), and anonymous journal reviewers contributed helpful comments that enhanced this work. ...

Maciej Radosz; Xudong Hu; Kaspars Krutkramelis; Youqing Shen

2008-04-29T23:59:59.000Z

403

Management of dry flue gas desulfurization by-products in underground mines. Topical report, October 1, 1993--March 31, 1998  

SciTech Connect (OSTI)

The DESEVAL-TRANS program is developed for the purpose of helping the engineer to design and economically evaluate coal combustion byproduct transportation systems that will operate between the power plant and the disposal site. The objective of the research project was to explore the technical, environmental and economic feasibility of disposing coal combustion byproducts in underground mines in Illinois. The DESEVAL-TRANS (short for Design and Evaluation of Transportation Systems) was developed in the Materials Handling and Systems Economics branch of the overall project. Four types of coal combustion byproducts were targeted for transportation and handling: Conventional fly ash; Scrubber sludge; Fluidized Bed Combustion (FBC) fly ash; and Spent-bed ash. Several transportation and handling systems that could handle these byproducts were examined. These technologies were classified under three general categories: Truck; Rail; and Container. The purpose of design models is to determine the proper number of transport units, silo capacity, loading and unloading rates, underground placement capacity, number of shifts, etc., for a given case, defined by a distance-tonnage combination. The cost computation models were developed for the determination of the operating and capital costs. An economic evaluation model, which is common to all categories, was also developed to establish the cost-per-ton of byproduct transported.

NONE

1998-09-01T23:59:59.000Z

404

Management of dry flue gas desulfurization by-products in underground mines. Technical progress report, 1 January--31 March 1994  

SciTech Connect (OSTI)

Southern Illinois University at Carbondale will develop and demonstrate several technologies for the handling and transport of dry coal combustion residues and for the underground placement in abandoned coal mines and assess associated environmental impacts. Although parts of the Residue Characterization portion of the program were delayed because residue samples were not obtained, other parts of the program are proceeding on schedule. The delays in obtaining residue samples were primarily caused by adverse weather conditions, the shut-down of one unit at the City Water, Light, and Power Company Plant for routing maintenance and problems due to conflicting schedules of utility and program personnel. However, by the end of the quarter most residue samples had been obtained, and the residue characterization studies were under way. Progress is described for five studies: environmental assessment and geotechnical stability and subsidence impacts; residue characterization; physico-chemical characterization of residues; identification and assessment of handling/transportation systems for FGD residues; and residue handling and transport.

Chugh, Y.P.; Esling, S.; Ghafoori, N.; Honaker, R.; Paul, B.; Sevim, H.; Thomasson, E.

1994-04-01T23:59:59.000Z

405

Flue Gas Emissions from the Burning of Asphaltite and Lignite in a Rotating Head Combustor with Secondary Air Delivery  

Science Journals Connector (OSTI)

(1, 2) In this context, Turkey is rich in coal reserves, and it is among the biggest coal producers in the world with a production of about 76 million tons (Mt) in 2011, and a large portion of this production is lignite. ... (5) Turkey has also a high asphaltite reserve, which is mostly found in the southeastern part of Anatolia and used around the region for domestic heating. ... Modeling of NOx emissions from fluidized Bed combustion of high volatile lignites ...

Cengiz Öner; ?ehmus Altun

2014-06-01T23:59:59.000Z

406

Photoactivated metal removal  

SciTech Connect (OSTI)

The authors propose the use of photochromic dyes as light activated switches to bind and release metal ions. This process, which can be driven by solar energy, can be used in environmental and industrial processes to remove metals from organic and aqueous solutions. Because the metals can be released from the ligands when irradiated with visible light, regeneration of the ligands and concentration of the metals may be easier than with conventional ion exchange resins. Thus, the process has the potential to be less expensive than currently used metal extraction techniques. In this paper, the authors report on their studies of the metal binding of spirogyran dyes and the hydrolytic stability of these dyes. They have prepared a number of spirogyrans and measured their binding constants for calcium and magnesium. They discuss the relationship of the structure of the dyes to their binding strengths. These studies are necessary towards determining the viability of this technique.

Nimlos, M.R.; Filley, J.; Ibrahim, M.A.; Watt, A.S.; Blake, D.M.

1999-07-01T23:59:59.000Z

407

Ozone removal by HVAC filters  

Science Journals Connector (OSTI)

Residential and commercial HVAC filters that have been loaded with particles during operation in the field can remove ozone from intake or recirculated air. However, knowledge of the relative importance of HVAC filters as a removal mechanism for ozone in residential and commercial buildings is incomplete. We measured the ozone removal efficiencies of clean (unused) fiberglass, clean synthetic filters, and field-loaded residential and commercial filters in a controlled laboratory setting. For most filters, the ozone removal efficiency declined rapidly but converged to a non-zero (steady-state) value. This steady-state ozone removal efficiency varied from 0% to 9% for clean filters. The mean steady-state ozone removal efficiencies for loaded residential and commercial filters were 10% and 41%, respectively. Repeated exposure of filters to ozone following a 24-h period of no exposure led to a regeneration of ozone removal efficiency. Based on a theoretical scaling analysis of mechanisms that are involved in the ozone removal process, we speculate that the steady-state ozone removal efficiency is limited by reactant diffusion out of particles, and that regeneration is due to internal diffusion of reactive species to sites available to ozone for reaction. Finally, by applying our results to a screening model for typical residential and commercial buildings, HVAC filters were estimated to contribute 22% and 95%, respectively, of total ozone removal in HVAC systems.

P. Zhao; J.A. Siegel; R.L. Corsi

2007-01-01T23:59:59.000Z

408

Removal of Xenon and Radon from Contaminated Atmospheres with Dioxygenyl Hexafluoroantimonate, O2SbF6  

Science Journals Connector (OSTI)

... process gas, and the excess fluorine must be removed afterwards. I have shown that radon, the heaviest noble gas, can be collected by oxidation with liquid bromine trifluoride and ... ). I report here further experiments with a dioxygenyl salt, O2SbF6, which reacts with radon and xenon at 25 C and which appears very promising as a reagent for removing ...

L. STEIN

1973-05-04T23:59:59.000Z

409

Oil shale retorting with steam and produced gas  

SciTech Connect (OSTI)

This patent describes a process for retorting oil shale in a vertical retort. It comprises introducing particles of oil shale into the retort, the particles of oil shale having a minimum size such that the particles are retained on a screen having openings 1/4 inch in size; contacting the particles of oil shale with hot gas to heat the particles of oil shale to a state of pyrolysis, thereby producing retort off-gas; removing the off-gas from the retort; cooling the off-gas; removing oil from the cooled off-gas; separating recycle gas from the off-gas, the recycle gas comprising steam and produced gas, the steam being present in amount, by volume, of at least 50% of the recycle gas so as to increase the yield of sand oil; and heating the recycle gas to form the hot gas.

Merrill, L.S. Jr.; Wheaton, L.D.

1991-08-20T23:59:59.000Z

410

Gas storage and separation by electric field swing adsorption  

DOE Patents [OSTI]

Gases are stored, separated, and/or concentrated. An electric field is applied across a porous dielectric adsorbent material. A gas component from a gas mixture may be selectively separated inside the energized dielectric. Gas is stored in the energized dielectric for as long as the dielectric is energized. The energized dielectric selectively separates, or concentrates, a gas component of the gas mixture. When the potential is removed, gas from inside the dielectric is released.

Currier, Robert P; Obrey, Stephen J; Devlin, David J; Sansinena, Jose Maria

2013-05-28T23:59:59.000Z

411

Removing Arsenic from Drinking Water  

ScienceCinema (OSTI)

See how INL scientists are using nanotechnology to remove arsenic from drinking water. For more INL research, visit http://www.facebook.com/idahonationallaboratory

None

2013-05-28T23:59:59.000Z

412

Removing Arsenic from Drinking Water  

SciTech Connect (OSTI)

See how INL scientists are using nanotechnology to remove arsenic from drinking water. For more INL research, visit http://www.facebook.com/idahonationallaboratory

None

2011-01-01T23:59:59.000Z

413

The Removal of Crude Oil in Waste Drilling Muds by a Constructed Microbial Consortium  

Science Journals Connector (OSTI)

Waste drilling muds (WDMs) contain serious pollutants produced by crude oil and gas well drilling. Bioremediation has been known as a useful ... enrichment of indigenous microorganisms, which can remove oil conta...

Yunkang Chang; Xingbiao Wang; Yifan Han…

2014-01-01T23:59:59.000Z

414

Trichloroethene Removal From Waste Gases in Anaerobic Biotrickling Filters Through Reductive Dechlorination  

E-Print Network [OSTI]

reductive dechlorination of PCE. Environ. Sci. Technol 2003,588. Kim, J. O. Gaseous TCE and PCE removal by an activatedTsotsis, T. T. Degradation of PCE in an anaerobic waste gas

Popat, Sudeep Chandrakant

2010-01-01T23:59:59.000Z

415

Liquid-Water Uptake and Removal in PEM Fuel-Cell Components  

E-Print Network [OSTI]

Uptake and Removal in PEM Fuel-Cell Components Prodip K. DasWater management in PEM fuel cells is critical for optimumof droplet dynamics in PEM fuel-cell gas flow channels has

Das, Prodip K.

2013-01-01T23:59:59.000Z

416

Gas well operation with liquid production  

SciTech Connect (OSTI)

Prediction of liquid loading in gas wells is discussed in terms of intersecting tubing or system performance curves with IPR curves and by using a more simplified critical velocity relationship. Different methods of liquid removal are discussed including such methods as intermittent lift, plunger lift, use of foam, gas lift, and rod, jet, and electric submersible pumps. Advantages, disadvantages, and techniques for design and application of the methods of liquid removal are discussed.

Lea, J.F.; Tighe, R.E.

1983-02-01T23:59:59.000Z

417

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

SciTech Connect (OSTI)

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.

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

2006-10-01T23:59:59.000Z

418

amine | netl.doe.gov  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

project that initiated development of a novel sorbent for the removal of carbon dioxide (CO2) from combustion flue gas. The primary goal of this project wa s to develop a process...

419

Removal of deposited copper from nuclear steam generators  

SciTech Connect (OSTI)

A review of the copper-removal process implemented during the cleaning of the NPD nuclear steam generator in Ontario revealed that major shortcomings in the process were depletion of the strong ammonia solution and relatively poor copper removal. Tests have shown that the concentration of the ammonia solution can be preserved close to its initial value, and high concentrations of complexed copper obtained, by sparging the ammonia solution with oxygen recirculating through a gas recirculation loop. Using recirculating oxygen for sparging at ambient air temperature, approximately 11 g/l of copper were dissolved by 100 g/l ammonia solution while the gaseous ammonia content of the recirculating gas remained well below the lower flammability limit. The corrosion rates of mild steel and commonly used nuclear steam generator tube materials in oxygenated ammonia solution were less than 30 mil/yr and no intergranular attack of samples was observed during tests. A second technique studied for the removal of copper is to ammoniate the spent iron-removal solvent to approximately pH 9.5 and sparge with recirculating oxygen. Complexed ferric iron in the spent iron-removal solvent was found to be the major oxidizing agent for metallic copper. The ferric iron can be derived from oxidation of dissolved ferrous iron to the ferric state or from dissolved oxides of iron directly. To extract copper from the secondary sides of nuclear steam generators, strong ammonia solution sparged with recirculating oxygen is recommended as the first stage, while ammoniated spent iron-removal solvent sparged with recirculating oxygen may be used to remove the copper freshly exposed during the removal of iron.

McSweeney, P.

1982-05-01T23:59:59.000Z

420

Alkaline sorbent injection for mercury control  

DOE Patents [OSTI]

A mercury removal system for removing mercury from combustion flue gases is provided in which alkaline sorbents at generally extremely low stoichiometric molar ratios of alkaline earth or an alkali metal to sulfur of less than 1.0 are injected into a power plant system at one or more locations to remove at least between about 40% and 60% of the mercury content from combustion flue gases. Small amounts of alkaline sorbents are injected into the flue gas stream at a relatively low rate. A particulate filter is used to remove mercury-containing particles downstream of each injection point used in the power plant system.

Madden, Deborah A. (Boardman, OH); Holmes, Michael J. (Washington Township, Stark County, OH)

2003-01-01T23:59:59.000Z