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Note: This page contains sample records for the topic "flue gas desulfurization" from the National Library of EnergyBeta (NLEBeta).
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1

Flue Gas Desulfurization Systems  

Science Conference Proceedings (OSTI)

In many of the operating flue gas desulfurization (FGD) systems throughout the world, materials corrosion leads to considerable costs and downtime. Utilities are often required to maintain, repair, replace, and/or upgrade existing materials to combat corrosion issues. This document provides the results of a recent EPRI survey that examined the various types of corrosion and materials damage in FGD systems.

2005-12-23T23:59:59.000Z

2

Flue gas desulfurization  

DOE Patents (OSTI)

The invention involves a combustion process in which combustion gas containing sulfur oxide is directed past a series of heat exchangers to a stack and in which a sodium compound is added to the combustion gas in a temparature zone of above about 1400 K to form Na/sub 2/SO/sub 4/. Preferably, the temperature is above about 1800 K and the sodium compound is present as a vapor to provide a gas-gas reaction to form Na/sub 2/SO/sub 4/ as a liquid. Since liquid Na/sub 2/SO/sub 4/ may cause fouling of heat exchanger surfaces downstream from the combustion zone, the process advantageously includes the step of injecting a cooling gas downstream of the injection of the sodium compound yet upstream of one or more heat exchangers to cool the combustion gas to below about 1150 K and form solid Na/sub 2/SO/sub 4/. The cooling gas is preferably a portion of the combustion gas downstream which may be recycled for cooling. It is further advantageous to utilize an electrostatic precipitator downstream of the heat exchangers to recover the Na/sub 2/SO/sub 4/. It is also advantageous in the process to remove a portion of the combustion gas cleaned in the electrostatic precipitator and recycle that portion upstream to use as the cooling gas. 3 figures.

Im, K.H.; Ahluwalia, R.K.

1984-05-01T23:59:59.000Z

3

Flue Gas Desulfurization Gypsum Agricultural Network  

Science Conference Proceedings (OSTI)

Research on flue gas desulfurization gypsum (FGDG) has been conducted under the auspices of the Flue Gas Desulfurization Gypsum Agricultural Network program sponsored by the Electric Power Research Institute (EPRI) in collaboration with individual utilities, the U.S. Environmental Protection Agency, U.S. Department of Agriculture-Agricultural Research Service, and universities. This report describes work conducted in northwestern New Mexico in 2008–2012 as part of that effort. Two separate ...

2012-10-15T23:59:59.000Z

4

Flue Gas Desulfurization Gypsum Agricultural Network  

Science Conference Proceedings (OSTI)

Increasing volumes of flue gas desulfurization (FGD) gypsum will become available for agricultural use as more utilities install forced oxidation scrubbers and the wallboard market for the resulting gypsum becomes saturated. This interim report describes work performed in 2007 and 2008 to develop a national research network to gain data and experience to support the beneficial uses of FGD products, especially FGD gypsum, in agriculture and other land applications.

2008-12-12T23:59:59.000Z

5

Flue Gas Desulfurization Equipment Issues Guidelines  

Science Conference Proceedings (OSTI)

As electric utilities enter a more competitive environment, every aspect of electric power generation is under scrutiny to determine where costs can be reduced. Because flue gas desulfurization (FGD) systems represent significant capital, operating, and maintenance expenses for many coal-fired power plants, identification and implementation of cost reduction options are crucial. This report documents successful approaches for determining the cost-effectiveness of key FGD optimization strategies.

2001-10-15T23:59:59.000Z

6

Flue Gas Desulfurization Gypsum Agricultural Network  

Science Conference Proceedings (OSTI)

Flue gas desulfurization (FGD) gypsum is a solid produced by wet FGD systems with forced air oxidation and is chemically similar to mined gypsum. These gypsums, used as beneficial agricultural amendments, were evaluated for their effects on earthworm populations and trace element concentrations in soils and earthworms at four field sites (Ohio, Indiana, Alabama, and Wisconsin). These sites are part of a network study on agricultural uses of FGD gypsum conducted at sites across the United States. ...

2012-09-19T23:59:59.000Z

7

Flue gas desulfurization wastewater treatment primer  

SciTech Connect

Purge water from a typical wet flue gas desulfurization system contains myriad chemical constituents and heavy metals whose mixture is determined by the fuel source and combustion products as well as the stack gas treatment process. A well-designed water treatment system can tolerate upstream fuel and sorbent arranged in just the right order to produce wastewater acceptable for discharge. This article presents state-of-the-art technologies for treating the waste water that is generated by wet FGD systems. 11 figs., 3 tabs.

Higgins, T.E.; Sandy, A.T.; Givens, S.W.

2009-03-15T23:59:59.000Z

8

Advanced Flue Gas Desulfurization (AFGD) Demonstration Project...  

NLE Websites -- All DOE Office Websites (Extended Search)

in the WES, which involves injection into the flue gas duct upstream of the existing electrostatic 11 precipitator (ESP). The hot flue gas evaporates the water and the...

9

Dry Flue Gas Desulfurization State of the Art Survey  

Science Conference Proceedings (OSTI)

The intent of this report is to provide a summary of state-of-the-art dry flue gas desulfurization (FGD) technologies, including circulating dry scrubbers (CDS), spray dryer absorbers (SDA), and the Alstom Novel Integrated Desulfurization (NID) technology. These can all be considered “semi-dry” technologies, as the flue gas is cooled and humidified as part of each of these processes. This report also discusses a completely dry FGD technology, dry sorbent injection (DSI), which is ...

2012-12-14T23:59:59.000Z

10

Flue gas desulfurization: Physicochemical and biotechnological approaches  

Science Conference Proceedings (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

11

Trace Metals Determination in Flue Gas Desulfurization Water  

Science Conference Proceedings (OSTI)

Flue gas desulfurization (FGD) scrubbers are used on coal-fired power plants to reduce sulfur dioxide emissions to air. While effective for this purpose, wet FGD scrubbers produce an aqueous blowdown stream that contains trace levels of metals adsorbed from flue gas. Power plant owners need to measure concentrations of these metals for purposes of process control, discharge monitoring, or design and operation of wastewater treatment systems. FGD water has proven to be a very difficult matrix to analyze a...

2009-12-28T23:59:59.000Z

12

Guidelines for Flue Gas Desulfurization (FGD) Water Sampling and Analysis  

Science Conference Proceedings (OSTI)

Flue gas desulfurization (FGD) scrubbers are being installed on coal-fired power plants in response to federal and state air pollution regulations limiting sulfur dioxide emissions. FGD scrubbers produce an aqueous waste stream that contains metals adsorbed from flue gas. At the same time, the U.S. Environmental Protection Agency (EPA) is reviewing, and may tighten, water discharge limits on trace metals. Collection of accurate data on the trace metal composition of FGD water discharges is therefore esse...

2009-03-27T23:59:59.000Z

13

Evaluation of Selenium Species in Flue Gas Desulfurization Waters  

Science Conference Proceedings (OSTI)

Flue gas desulfurization (FGD) is a process used in the electrical power industry to remove sulfur dioxide from flue gas produced by coal-fired power plants. The trace element selenium is found in coal and can become concentrated in the wastewater from the FGD process. Some chemical forms, or species, of selenium are more resistant to removal by water treatment processes than others; thus, understanding the speciation of selenium is important to designing effective wastewater treatment systems. In additi...

2009-03-23T23:59:59.000Z

14

Identification of Unknown Selenium Species in Flue Gas Desulfurization Water  

Science Conference Proceedings (OSTI)

Flue gas desulfurization (FGD) is a process used in the electrical power industry to remove sulfur dioxide (SO2) from flue gas produced by coal-fired power plants. In a wet FGD system, circulating water must be periodically blown down and treated to remove solids and dissolved chemicals. Along with SO2, other substances in flue gas may dissolve in water, including selenium (Se). In addition to the common selenium species selenite and selenate, past research has identified selenium-containing species that...

2008-03-25T23:59:59.000Z

15

Process for the desulfurization of flue gas  

SciTech Connect

A process for the removal of sulfur oxides from gases is described that is comprised of the steps of contacting the gas with a cerium oxide sorbent at conditions whereby the sulfur oxides present in the gas are sorbed by the cerium oxide sorbent and regenerate the cerium oxide sorbent by contacting it with a reducing atmosphere at conditions whereby the sorbent is substantially converted to a sulfur-free state. The gas may be an exhaust gas, e.g., from an automobile or a flue gas. This invention is especially preferred for treating flue gas. In this preferred embodiment, the flue gas may be contacted with the cerium oxide sorbent at a temperature of from 300/sup 0/ to 800/sup 0/C, to form cerium sulfate and/or sulfite and the sorbent is regenerated by contacting with a reducing gas, for example, hydrogen in admixture with steam or other inert gases at a temperature of from 500/sup 0/ to 800/sup 0/C to convert the cerium sulfate or sulfite to cerium oxide. During the regeneration step, the desorbed species is initially sulfur dioxide. However, when about 50% of the sulfur is removed from the sorbent, the desorbed species becomes H/sub 2/S. Thus, the instant invention provides SO/sub 2/ and H/sub 2/S in admixture with the excess reducing gas, which can be fed conveniently to the Claus plant for conversion into elemental sulfur.

Longo, J.M.

1977-01-04T23:59:59.000Z

16

Carbon Dioxide Sequestration with Flue Gas Desulfurization (FGD) Gypsum  

Science Conference Proceedings (OSTI)

Carbonation of industrial alkaline residues can be used as a CO2 sequestration technology to reduce carbon dioxide emissions. In this study, alkaline Ca-rich flue gas desulfurization (FGD) gypsum samples were carbonated to a varying extent. These materials ... Keywords: FGD gypsum, carbonation, carbon dioxide

Hongqi Wang; Ningning Sun; Rona J. Donahoe

2009-07-01T23:59:59.000Z

17

Flue Gas Desulfurization Scrubber Maintenance Guide: Gypsum Dewatering Area  

Science Conference Proceedings (OSTI)

Flue Gas Desulfurization Scrubber Maintenance Guide: Gypsum Dewatering Area provides fossil plant maintenance personnel with current maintenance information on this system. This report will assist the plant maintenance personnel in improving the reliability and reducing the maintenance costs for this area of their scrubber system.

2009-12-08T23:59:59.000Z

18

Flue Gas Desulfurization Scrubber Maintenance Guide: Absorber Area  

Science Conference Proceedings (OSTI)

The Flue Gas Desulfurization Scrubber Maintenance Guide: Absorber Area provides fossil plant maintenance personnel with current maintenance information on this system and will help to improve the reliability of and reduce the maintenance costs for this area of their scrubber system.

2008-12-18T23:59:59.000Z

19

Investigation of Flue Gas Desulfurization Chemical Process Problems  

Science Conference Proceedings (OSTI)

An understanding of flue gas desulfurization process chemistry is crucial in troubleshooting problems in operating FGD systems. This report discusses a variety of problems and solutions associated with process chemistry for 25 different wet FGD systems, including lime/limestone and double alkali processes. Among the problems addressed are SO2 removal, mist eliminator scaling, poor solids dewatering, and water management.

1990-09-10T23:59:59.000Z

20

Flue Gas Desulfurization Scrubber Maintenance Guide: Reagent Preparation Area  

Science Conference Proceedings (OSTI)

The Flue Gas Desulfurization Scrubber Maintenance Guide: Reagent Preparation Area provides the fossil plant maintenance personnel with current maintenance information on this system and will help improve the reliability and reduce the maintenance costs for this area of their scrubber system.

2008-12-15T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

Flue Gas Desulfurization (FGD) Wastewater Characterization and Management: 2007 Update  

Science Conference Proceedings (OSTI)

Tightened air regulations on acid-gas-forming emissions are leading more electric utilities to install flue gas desulfurization (FGD) systems, typically wet scrubbers. However, there are challenges associated with such decisions in terms of utility wastewater management. Volatile metals, such as selenium and mercury, are better captured in wet scrubber systems than in electrostatic precipitators and may be present at higher concentrations in utility wastewater systems. This report is designed to help pow...

2008-03-31T23:59:59.000Z

22

2009 Update on Mercury Capture by Wet Flue Gas Desulfurization  

Science Conference Proceedings (OSTI)

This technical update presents results of four research and development projects focused on understanding and enhancing mercury emissions control associated with wet flue gas desulfurization (FGD) technology. The first project was directed at characterizing partitioning of elemental and oxidized mercury species in solid, liquid, and gas phases within process streams involved in an operating commercial system. The second project explored dewatering options with an objective of producing low-mercury-conten...

2009-12-15T23:59:59.000Z

23

Air Toxics Control by Wet Flue Gas Desulfurization Systems  

Science Conference Proceedings (OSTI)

This report provides an update on three tasks associated with the EPRI project, Air Toxics Control by Wet Flue Gas Desulfurization (FGD) Systems. The first task is an investigation of the factors that influence and control the oxidation-reduction potential (ORP) at which a limestone forced oxidation FGD system operates. Both a literature review and a numerical analysis of full-scale wet FGD data were conducted. Results from this task are presented and discussed in Section 2 of the ...

2012-12-31T23:59:59.000Z

24

Spray tower: the workhorse of flue-gas desulfurization  

Science Conference Proceedings (OSTI)

A recently developed spray tower system for use in a utility flue gas desulfurization system is simple, durable, and capable of achieving very high sulfur dioxide removal efficiencies, possibly approaching 100%. The principles behind the design and operation of the spray tower are discussed. The quality of water used for washing, tower size limitations, construction materials liquid distribution, gas-inlet design, gas distribution, mass transfer, and operating characteristics are examined. Procedures to maintain the reliability and high performance of the spray tower are described. (5 diagrams, 5 photos, 12 references, 1 table)

Saleem, A.

1980-10-01T23:59:59.000Z

25

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

NLE Websites -- All DOE Office Websites (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

26

The durability of stabilized flue gas desulfurization sludge  

Science Conference Proceedings (OSTI)

The effects of freeze-thaw cycling on the strength and durability of samples of compacted, stabilized, wet flue gas desulfurization (FGD) by-products are reported. The results of laboratory tests show a clear relationship between higher water contents and increasing vulnerability to freeze-thaw effects. In the samples tested, water contents at or above 40% were characteristic of all the freeze-thaw specimens exhibiting low strengths. Lime content and curing time were also shown to have a marked influence on the durability of the FGD material. It was shown that samples can maintain good strength under freeze-thaw conditions provided 5% lime was added before compaction and the time from compaction to first freeze was at least 60 days.

Chen, X.; Wolfe, W.E.; Hargraves, M.D.

1995-12-31T23:59:59.000Z

27

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

28

A Review of Manufacturing Uses for Gypsum Produced by Flue Gas Desulfurization Systems  

Science Conference Proceedings (OSTI)

Gypsum is widely used as a source material to manufacture products for building construction applications8212primarily wallboard, cement, and concrete8212and has a number of other commercial applications. The mineral is mined throughout the world (natural gypsum) and also is produced as a result of various industrial processes (synthetic gypsum). The largest source of synthetic gypsum used for manufacturing applications is flue gas desulfurization (FGD) gypsum, the product of wet flue gas desulfurization...

2006-03-07T23:59:59.000Z

29

Flue Gas Desulfurization Gypsum Agricultural Network: Indiana Kingman Research Station (Corn and Soybeans)  

Science Conference Proceedings (OSTI)

Flue gas desulfurization gypsum (FGDG) is an excellent source of gypsum (CaSO4•2H2O) that is created when sulfur dioxide is removed from the exhaust gases during the combustion of coal for energy production. Research on FGDG has been conducted as part of the Flue Gas Desulfurization Gypsum Agricultural Network program sponsored by the Electric Power Research Institute in collaboration with individual utilities, the U.S. EPA, the United States Department of Agriculture’s Agricultural ...

2013-10-07T23:59:59.000Z

30

Economic assessment of advanced flue gas desulfurization processes. Final report  

Science Conference Proceedings (OSTI)

This report presents the results of a project sponsored by the Morgantown Energy Technology Center (METC). The purpose of the study was to perform an economic and market assessment of advanced flue gas desulfurization (FGD) processes for application to coal-fired electric utility plants. The time period considered in the study is 1981 through 1990, and costs are reported in 1980 dollars. The task was divided into the following four subtasks: (1) determine the factors affecting FGD cost evaluations; (2) select FGD processes to be cost-analyzed; (3) define the future electric utility FGD system market; and (4) perform cost analyses for the selected FGD processes. The study was initiated in September 1979, and separate reports were prepared for the first two subtasks. The results of the latter two subtasks appear only in this final reprot, since the end-date of those subtasks coincided with the end-date of the overall task. The Subtask 1 report, Criteria and Methods for Performing FGD Cost Evaluations, was completed in October 1980. A slightly modified and condensed version of that report appears as appendix B to this report. The Subtask 2 report, FGD Candidate Process Selection, was completed in January 1981, and the principal outputs of that subtask appear in Appendices C and D to this report.

Bierman, G. R.; May, E. H.; Mirabelli, R. E.; Pow, C. N.; Scardino, C.; Wan, E. I.

1981-09-01T23:59:59.000Z

31

PRODUCTION OF CONSTRUCTION AGGREGATES FROM FLUE GAS DESULFURIZATION SLUDGE  

SciTech Connect

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.

1998-12-01T23:59:59.000Z

32

Evaluation of the NeuStream-S™ Flue Gas Desulfurization Process  

Science Conference Proceedings (OSTI)

Harris Group Inc. (HGI) of Denver, Colorado, was contracted by the Electric Power Research Institute (EPRI) to monitor, evaluate, and prepare this report on a dual-alkali flue gas desulfurization (FGD) process developed by Neumann Systems Group, Inc. (NSG). The process is being demonstrated in a nominal 20-MW demonstration plant, treating a slip stream of flue gas from the Colorado Springs Utilities 142-MW Drake Unit 7. HGI evaluated performance, operability, and readiness for scale-up of the process. Co...

2011-05-31T23:59:59.000Z

33

Enhanced Control of Mercury by Wet Flue Gas Desulfurization Systems - Site 3 Topical Report  

Science Conference Proceedings (OSTI)

Researchers conducted field tests to evaluate the ability of a variety of materials to oxidize vapor-phase elemental mercury at a coal-fired power plant equipped with a wet flue gas desulfurization (FGD) system. Results, while confounded by measurement difficulties, showed that under bituminous coal flue gas conditions, two catalysts, Pd #1 and Carbon #6, continued to oxidize at least 85 percent of the inlet elemental mercury after three months.

2002-02-06T23:59:59.000Z

34

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

35

BUILDING MATERIALS MADE FROM FLUE GAS DESULFURIZATION BY-PRODUCTS  

SciTech Connect

Flue gas desulphurization (FGD) materials are produced in abundant quantities by coal burning utilities. Due to environmental restrains, flue gases must be ''cleaned'' prior to release to the atmosphere. They are two general methods to ''scrub'' flue gas: wet and dry. The choice of scrubbing material is often defined by the type of coal being burned, i.e. its composition. Scrubbing is traditionally carried out using a slurry of calcium containing material (slaked lime or calcium carbonate) that is made to contact exiting flue gas as either a spay injected into the gas or in a bubble tower. The calcium combined with the SO{sub 2} in the gas to form insoluble precipitates. Some plants have been using dry injection of these same materials or their own Class C fly ash to scrub. In either case the end product contains primarily hannebachite (CaSO{sub 3} {center_dot} 1/2H{sub 2}O) with smaller amounts of gypsum (CaSO{sub 4} {center_dot} 2H{sub 2}O). These materials have little commercial use. Experiments were carried out that were meant to explore the feasibility of using blends of hannebachite and fly ash mixed with concentrated sodium hydroxide to make masonry products. The results suggest that some of these mixtures could be used in place of conventional Portland cement based products such as retaining wall bricks and pavers.

Michael W. Grutzeck; Maria DiCola; Paul Brenner

2006-03-30T23:59:59.000Z

36

Land Application Uses for Dry Flue Gas Desulfurization By-Products: Phase 2  

Science Conference Proceedings (OSTI)

The utility industry currently generates about 20 million tons of flue gas desulfurization (FGD) by-products annually, and the quantity is expected to increase as utilities institute further controls to comply with Clean Air Act requirements. This report presents the results of the second phase of a large-scale study of beneficial land-use applications of these by-products.

1998-04-10T23:59:59.000Z

37

Flue Gas Desulfurization Scrubber Maintenance Guide: Wastewater Treatment and Gypsum Handling Area  

Science Conference Proceedings (OSTI)

The Flue Gas Desulfurization Scrubber Maintenance Guide: Wastewater Treatment and Gypsum Handling Area provides fossil plant maintenance personnel with current maintenance information on these systems. This guide will assist plant maintenance personnel in improving the reliability and reducing the maintenance costs for these areas of their scrubber system.

2009-12-23T23:59:59.000Z

38

Stabilization of Flue Gas Desulfurization Sludge for Application in Marine Environments.  

E-Print Network (OSTI)

??Flue Gas Desulfurization sludge (FGD, CaSO4·2H2O, CaSO3·1/2H2O) is a waste by-product produced when sorbent slurry is passed through wet scrubbers. FGD contains higher concentrations of… (more)

Kour, Tej

2004-01-01T23:59:59.000Z

39

Thermal Flue Gas Desulfurization Wastewater Treatment Processes for Zero Liquid Discharge Operations  

Science Conference Proceedings (OSTI)

This report presents a worldwide inventory of power plant flue gas desulfurization (FGD) blowdown treatment systems using thermal technologies to achieve zero liquid discharge (ZLD) water management. The number of thermal treatment systems presently operating is very few, with the majority using chemical pretreatment followed by evaporation in a brine concentrator and crystallizer and finally dewatering of the residual salts. Of the operating thermal ZLD systems identified, six are located in Italy and o...

2010-12-31T23:59:59.000Z

40

Flue Gas Desulfurization Gypsum Agricultural Network: North Dakota Sites 1 and 2 (Wheat)  

Science Conference Proceedings (OSTI)

This report describes work performed in 2007 and 2008 to evaluate potential beneficial agricultural uses of flue gas desulfurization (FGD) gypsum at two sites in North Dakota. This work was part of a national research network evaluating beneficial uses of FGD gypsum in agriculture. The objectives of this research were to determine the influence of FGD gypsum applications on soil quality and on wheat (Triticum aestivum L.) yields and seed quality. Three application rates of FGD gypsum were compared with s...

2011-12-16T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

Performance Evaluation of a Radial Deionization System for Flue Gas Desulfurization Wastewater Treatment  

Science Conference Proceedings (OSTI)

The U. S. Environmental Protection Agency’s proposed effluent limitation guidelines for steam electric power generating units could affect not only how power plants use water but also how they discharge it. The revised guidelines propose discharge limits for selenium, mercury, arsenic, and nitrite/nitrate in flue gas desulfurization (FGD) wastewater. Final rule approval is expected by the middle of 2014. Additional regulation of these contaminants and other constituents may occur through ...

2013-12-23T23:59:59.000Z

42

Land Application Uses for Dry Flue Gas Desulfurization By-Products: Phase 3  

Science Conference Proceedings (OSTI)

The utility industry currently generates about 25 million tons of flue gas desulfurization (FGD) by-products annually in the United States -- a quantity that is expected to increase as utilities apply new controls to comply with Clean Air Act Amendments. This report presents results of the third and final phase of a large-scale study of beneficial land-use applications for these by-products.

1999-09-28T23:59:59.000Z

43

A Review of Agricultural and Other Land Application Uses of Flue Gas Desulfurization Products  

Science Conference Proceedings (OSTI)

The production of flue gas desulfurization (FGD) products, especially FGD gypsum, is expected to increase substantially over the next ten to twenty years in response to clean air initiatives. There are a large number of agricultural and other land application uses of FGD products that have received previous research and development attention, but only in specific locations of the United States and under limited conditions of crops, climate and soil types. This report discusses current and potential futur...

2006-03-13T23:59:59.000Z

44

Demonstration Test of Iron Addition to a Flue Gas Desulfurization (FGD) Absorber to Enhance Mercury Removal  

Science Conference Proceedings (OSTI)

This report documents the findings from a full-scale demonstration test of the effects on trace elements of adding iron to a forced oxidation flue gas desulfurization (FGD) scrubber. Three specific effects were evaluated: lowering mercury emissions to the atmosphere; lowering the concentration of soluble or sub-micron-sized mercury particles in FGD purge water, which could improve removal of mercury in FGD purge water treatment; and lowering the concentration of selenate in FGD purge water, which could i...

2009-12-31T23:59:59.000Z

45

Land Application Uses for Dry Flue Gas Desulfurization By-Products  

Science Conference Proceedings (OSTI)

New sulfur dioxide removal technologies produce a dry, solid by-product material consisting of excess sorbent, reaction products that contain sulfates and sulfites, and coal fly ash. The scarcity of landfill disposal sites for such flue gas desulfurization (FGD) by-products has led to a long-term study on possible large-volume beneficial applications. To date, FGD by-products have been successfully used in agriculture, construction, and strip mine reclamation.

1995-09-26T23:59:59.000Z

46

The Fate of Mercury Absorbed in Flue Gas Desulfurization (FGD) Systems  

Science Conference Proceedings (OSTI)

Wet flue gas desulfurization (FGD) systems are known to remove a percentage of the mercury in coal flue gases. This raises several questions about the fate of mercury removed by wet FGD systems: Does the absorbed mercury stay in the FGD liquor or does it leave with the byproduct solids? What happens to mercury in the FGD liquor and solid byproducts when they leave the FGD system? To address such questions, this report describes results from an EPRI project that involves field sample collection and labora...

2005-03-24T23:59:59.000Z

47

Model predictive control of a wet limestone flue gas desulfurization pilot plant  

SciTech Connect

A model predictive control (MPC) strategy based on a dynamic matrix (DMC) is designed and applied to a wet limestone flue gas desulfurization (WLFGD) pilot plant to evaluate what enhancement in control performance can be achieved with respect to a conventional decentralized feedback control strategy. The results reveal that MPC can significantly improve both reference tracking and disturbance rejection. For disturbance rejection, the main control objective in WLFGD plants, selection of tuning parameters and sample time, is of paramount importance due to the fast effect of the main disturbance (inlet SO{sub 2} load to the absorber) on the most important controlled variable (outlet flue gas SO{sub 2} concentration). The proposed MPC strategy can be easily applied to full-scale WLFGD plants.

Perales, A.L.V.; Ollero, P.; Ortiz, F.J.G.; Gomez-Barea, A. [University of Seville, Seville (Spain). Dept. of Chemical & Environmental Engineering

2009-06-15T23:59:59.000Z

48

Reclamation of abandoned surface coal mined land using flue gas desulfurization products  

SciTech Connect

Details are given of a field-scale research project where the Fleming site, in Ohio, of highly degraded and acid-forming abandoned surface coal-mined land, was reclaimed using a dry flue gas desulfurization product from an atmospheric fluidized bed combustion burner at a General Motors plant Pontiac, MI, which burned eastern Ohio coal and used dolomitic limestone for desulfurization. Plots were seeded with a mixture of grasses, wheat and clover, in 1994 and soil and water samples were analysed in 1995 and in 2009. It was found that FGD-treated plots promoted good regenerative growth, similar to that in plots using more concentrated re-soil material. The FGD treatment also greatly improved overall water quality. 3 figs., 4 tabs.

Chen, L.; Kost, D.; Dick, W.A. [Ohio State University, OH (United States)

2009-07-01T23:59:59.000Z

49

Leaching Assessment of Fly Ash, Flue Gas Desulfurization Filter Cake, and Fixated Scrubber Solids  

Science Conference Proceedings (OSTI)

The by-products of coal combustion (for example, fly ash and flue gas desulfurization filter cake) are an important environmental concern due to potential leaching of trace constituents and the large volume of residues produced. About 40% of these by-products may be utilized as raw materials outside of the energy sector; the remaining 60% of the coal combustion products (CCPs) are disposed of as waste. At Plant 14090, the subject of this report, fly ash and scrubber sludge are blended with quicklime ...

2012-12-03T23:59:59.000Z

50

Flue Gas Desulfurization Gypsum Agricultural Network: Wisconsin Arlington Research Station Fields 295 and 27 (Alfalfa)  

Science Conference Proceedings (OSTI)

This report describes field research in Wisconsin as part of the Flue Gas Desulfurization Gypsum (FGDG) Agricultural Network. The objective of this study, conducted during 2009-2010, was to evaluate potential beneficial agricultural uses of FGDG as a soil amendment to improve alfalfa production. FGDG was compared to a commercially available gypsum product (C-GYP) widely sold in the U.S. Midwest and other areas. A study was established in two fields (Field 295 in 2009/2010 and Field 27 in 2010) at ...

2013-05-06T23:59:59.000Z

51

Flue Gas Desulfurization Gypsum Agricultural Network: North Dakota Sites 3, 4, and 5 (Canola)  

Science Conference Proceedings (OSTI)

Flue gas desulfurization gypsum (FGDG) is a very pure form of gypsum that is a by-product from the combustion of coal for energy production. This report describes 2008-2009 work to evaluate potential beneficial agricultural uses of FGDG at three sites near Langdon, North Dakota. This work was part of a national research network evaluating beneficial uses of FGDG in agriculture, in this case, fertilization of dryland canola by FGDG. The objectives of this research were to 1) determine the influence of FGD...

2011-11-28T23:59:59.000Z

52

Enhanced Control of Mercury by Wet Flue Gas Desulfurization Systems - Site 2 Results  

Science Conference Proceedings (OSTI)

The U.S. Department of Energy and EPRI are co-funding this project to improve the control of mercury emissions from coal-fired power plants equipped with wet flue gas desulfurization (FGD) systems. The project is investigating 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 installation...

2000-11-28T23:59:59.000Z

53

Inductively Coupled Plasma-Mass Spectrometry with Collision/Reaction Cell Technology for Analysis of Flue Gas Desulfurization Wastew aters  

Science Conference Proceedings (OSTI)

Flue gas desulfurization (FGD) wastewater is produced by pollution control equipment used on coal-fired power plants to reduce sulfur dioxide emissions to air. Wet FGD scrubbers produce an aqueous blowdown stream that contains trace levels of metals that have been adsorbed from flue gas. Power plant owners need to measure concentrations of these metals for purposes of process control, discharge monitoring, or design and operation of wastewater treatment systems. FGD water is a very difficult matrix ...

2012-09-20T23:59:59.000Z

54

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

Science Conference Proceedings (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

55

Characteristics and reactivity of rapidly hydrated sorbent for semidry flue gas desulfurization  

Science Conference Proceedings (OSTI)

The semidry flue gas desulfurization (FGD) process has many advantages over the wet FGD process for moving sulfur dioxide emissions from pulverized coal-fired power plants. Semidry FGD with a rapidly hydrated sorbent was studied in a pilot-scale circulating fluidized bed (CFB) experimental facility. The sorbent was made from lumps of lime and coal fly ash. The desulfurization efficiency was measured for various operating parameters, including the sorbent recirculation rate and the water spray method. The experimental results show that the desulfurization efficiencies of the rapidly hydrated sorbent were 1.5-3.0 times higher than a commonly used industrial sorbent for calcium to sulfur molar ratios from 1.2 to 3.0, mainly due to the higher specific surface area and pore volume. The Ca(OH){sub 2} content in the cyclone separator ash was about 2.9% for the rapidly hydrated sorbent and was about 0.1% for the commonly used industrial sorbent, due to the different adhesion between the fine Ca(OH){sub 2} particles and the fly ash particles, and the low cyclone separation efficiency for the fine Ca(OH){sub 2} particles that fell off the sorbent particles. Therefore the actual recirculation rates of the active sorbent with Ca(OH){sub 2} particles were higher for the rapidly hydrated sorbent, which also contributed to the higher desulfurization efficiency. The high fly ash content in the rapidly hydrated sorbent resulted in good operating stability. The desulfurization efficiency with upstream water spray was 10-15% higher than that with downstream water spray. 20 refs., 7 figs., 1 tab.

Jie Zhang; Changfu You; Suwei Zhao; Changhe Chen; Haiying Qi [Tsinghua University, Beijing (China). Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Thermal Engineering

2008-03-01T23:59:59.000Z

56

Pilot-plant technical assessment of wet flue gas desulfurization using limestone  

Science Conference Proceedings (OSTI)

An experimental study was performed on a countercurrent pilot-scale packed scrubber for wet flue gas desulfurization (FGD). The flow rate of the treated flue gas was around 300 Nm{sup 3}/h, so the pilot-plant capacity is one of the largest with respect to other published studies on a pilot-plant wet FGD. The tests were carried out at an SO{sub 2} inlet concentration of 2000 ppm by changing the recycle slurry pH to around 4.8 and the L/G ratio to between 7.5 and 15. Three types of limestone were tested, obtaining desulfurization efficiencies from 59 to 99%. We show the importance of choosing an appropriate limestone in order to get a better performance from the FGD plant. Thus, it is important to know the reactivity (on a laboratory scale) and the sorbent utilization (on a pilot-plant scale) in order to identify if a limestone is reactive enough and to compare it with another type. In addition, by using the transfer-unit concept, a function has been obtained for the desulfurization efficiency, using the L/G ratio and the recycle slurry pH as independent variables. The Ca/S molar ratio is related to these and to the SO{sub 2} removal efficiency. This function, together with a simplified function of the operation variable cost, allows us to determine the pair (L/G ratio and pH) to achieve the desired SO{sub 2} removal with the minimum operation cost. Finally, the variable operation costs between packed towers and spray scrubbers have been compared, using as a basis the pilot packed tower and the industrial spray column at the Compostilla Power Station's FGD plant (in Leon, Spain).

Ortiz, F.J.G.; Vidal, F.; Ollero, P.; Salvador, L.; Cortes, V.; Gimenez, A. [University of Seville, Seville (Spain)

2006-02-15T23:59:59.000Z

57

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 (gypsum). Fuel ashes result from the burning of coal. Gypsum is a byproduct of the air purification system, called Flue Gas Desulfurization (FGD). Abatement of these waste products is a growing concern, not only for the industry, but the environment as well. It is possible to produce a gypsum brick unit that can meet the engineering properties required by the Americans Society of Testing Materials (ASTM) standards by using these by-products. This can be accomplished at a cost less than the least expensive common fired clay brick that is used in construction operations. The gypsum brick can be manufactured using established methods that are currently in operation.

Berryman, Charles Wayne

1992-01-01T23:59:59.000Z

58

Controllability analysis and decentralized control of a wet limestone flue gas desulfurization plant  

Science Conference Proceedings (OSTI)

Presently, decentralized feedback control is the only control strategy used in wet limestone flue gas desulfurization (WLFGD) plants. Proper tuning of this control strategy is becoming an important issue in WLFGD plants because more stringent SO{sub 2} regulations have come into force recently. Controllability analysis is a highly valuable tool for proper design of control systems, but it has not been applied to WLFGD plants so far. In this paper a decentralized control strategy is designed and applied to a WLFGD pilot plant taking into account the conclusions of a controllability analysis. The results reveal that good SO{sub 2} control in WLFGD plants can be achieved mainly because the main disturbance of the process is well-aligned with the plant and interactions between control loops are beneficial to SO{sub 2} control.

Perales, A.L.V.; Ortiz, F.J.G.; Ollero, P.; Gil, F.M. [University of Seville, Seville (Spain)

2008-12-15T23:59:59.000Z

59

Effect of H{sub 2}O on the desulfurization of simulated flue gas by an ionic liquid  

SciTech Connect

Functionalized ionic liquids (ILs) have been demonstrated to absorb SO{sub 2} from mixed gases or simulated flue gases efficiently. However, after absorbing a large amount of SO{sub 2}, the viscosity of the ILs increases greatly, which might limit their eventual applications in large-scale desulfurization from mixed gases or flue gases. In this work, the effect of the presence of water in a simulated flue gas on the absorption of SO{sub 2} by a functionalized ionic liquid, 1,1,3,3-tetramethylguanidinium lactate, has been studied at different temperatures. It is found that the presence of water in the simulated flue gas can decrease the viscosity of the IL greatly, and it has no effect on the absorptivity of SO{sub 2} from the flue gas. The densities of the IL absorbing SO{sub 2} from the flue gas with or without water are also studied. They increase with the increase of the amount of SO{sub 2} absorbed from the flue gas in both cases.

Ren, S.H.; Hou, Y.C.; Wu, W.Z.; Chen, X.T.; Fan, J.L.; Zhang, J.W. [Beijing University of Chemical Technology, Beijing (China)

2009-05-15T23:59:59.000Z

60

Corrosion in Wet Flue Gas Desulfurization (FGD) Systems: Technical Root Cause Analysis of Internal Corrosion on Wet FGD Alloy Absorbers  

Science Conference Proceedings (OSTI)

State-of-the-art flue gas desulfurization (FGD) technologies have been or are being installed on most large coal-fired electric generating units in response to new regulatory emission requirements. Aggressive corrosion has been noted in some of these systems, presumably from the low pH, high chloride environments created in the FGD process. There exists a plethora of material systems (metallic, organic, plastics, coating, and so forth) available to construct these systems, but, because of cost, fabricabi...

2012-04-30T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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
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61

Evaluation of the Origin of Dissolved Organic Carbon and the Treatability of Mercury in Flue Gas Desulfurization Wastewater  

Science Conference Proceedings (OSTI)

Regulations for reducing the dissolved mercury (Hg) concentrations in wastewater discharged by electric generating power plants are becoming more stringent via federal regulatory limits proposed by the EPA and regulatory limits set by select states. Data obtained in a previous EPRI study conducted in 2009 suggested a potential negative impact of dissolved organic carbon (DOC) and iodide concentrations present in flue gas desulfurization (FGD) wastewater on mercury treatability (EPRI report 1019867). ...

2013-12-17T23:59:59.000Z

62

Advanced Flue Gas Desulfurization (AFGD) demonstration project: Volume 2, Project performance and economics. Final technical report  

SciTech Connect

The project objective is to demonstrate removal of 90--95% or more of the SO{sub 2} at approximately one-half the cost of conventional scrubbing technology; and to demonstrate significant reduction of space requirements. In this project, Pure Air has built a single SO{sub 2} absorber for a 528-MWe power plant. The absorber performs three functions in a single vessel: prequencher, absorber, and oxidation of sludge to gypsum. Additionally, the absorber is of a co- current design, in which the flue gas and scrubbing slurry move in the same direction and at a relatively high velocity compared to conventional scrubbers. These features all combine to yield a state- of-the-art SO{sub 2} absorber that is more compact and less expensive than conventional scrubbers. The project incorporated a number of technical features including the injection of pulverized limestone directly into the absorber, a device called an air rotary sparger located within the base of the absorber, and a novel wastewater evaporation system. The air rotary sparger combines the functions of agitation and air distribution into one piece of equipment to facilitate the oxidation of calcium sulfite to gypsum. Additionally, wastewater treatment is being demonstrated to minimize water disposal problems inherent in many high-chloride coals. Bituminous coals primarily from the Indiana, Illinois coal basin containing 2--4.5% sulfur were tested during the demonstration. The Advanced Flue Gas Desulfurization (AFGD) process has demonstrated removal of 95% or more of the SO{sub 2} while providing a commercial gypsum by-product in lieu of solid waste. A portion of the commercial gypsum is being agglomerated into a product known as PowerChip{reg_sign} gypsum which exhibits improved physical properties, easier flowability and more user friendly handling characteristics to enhance its transportation and marketability to gypsum end-users.

NONE

1996-04-30T23:59:59.000Z

63

Investigation of a mercury speciation technique for flue gas desulfurization materials  

Science Conference Proceedings (OSTI)

Most of the synthetic gypsum generated from wet flue gas desulfurization (FGD) scrubbers is currently being used for wallboard production. Because oxidized mercury is readily captured by the wet FGD scrubber, and coal-fired power plants equipped with wet scrubbers desire to benefit from the partial mercury control that these systems provide, some mercury is likely to be bound in with the FGD gypsum and wallboard. In this study, the feasibility of identifying mercury species in the FGD gypsum and wallboard samples was investigated using a large sample size thermal desorption method and samples from power plants in Pennsylvania. Potential candidates of pure mercury standards including mercuric chloride, mercurous chloride, mercury oxide, mercury sulfide, and mercuric sulfate were analyzed to compare their results with those obtained from FGD gypsum and dry wallboard samples. Although any of the thermal evolutionary curves obtained from these pure mercury standards did not exactly match with those of the FGD gypsum and wallboard samples, it was identified that Hg{sub 2}Cl{sub 2} and HgCl{sub 2} could be candidates. An additional chlorine analysis from the gypsum and wallboard samples indicated that the chlorine concentrations were approximately 2 orders of magnitude higher than the mercury concentrations, suggesting possible chlorine association with mercury. 21 refs., 5 figs., 3 tabs.

Lee, J.Y.; Cho K.; Cheng L.; Keener, T.C.; Jegadeesan G.; Al-Abed, S.R. [University of Cincinnati, Cincinnati, OH (United States). Department of Chemical and Materials Engineering

2009-08-15T23:59:59.000Z

64

Recycle/reuse of boiler chemical cleaning wastes in wet limestone flue gas desulfurization (FGD) systems  

Science Conference Proceedings (OSTI)

Boiler chemical cleaning wastes (BCCW) are generated by the periodic waterside cleaning of utility boilers to remove metallic deposits from boiler tube surfaces. Depending on boiler metallurgy, BCCW generally contain high concentrations of iron and copper or both, as well as other heavy metals such as chromium, lead, nickel, and zinc. BCCW treatment and disposal methods include precipitation, coponding in an ash pond, evaporation in the fireside of an operating boiler (for organic solvents), and contracted off-site disposal. Depending on the type of BCCW chemical treatment methods achieve varying degrees of success. BCCW which contain organic chelating agents can be especially difficult to treat to national pollutant discharge elimination system (NPDES) limits (1 mg/L for both iron and copper) with conventional lime precipitation.Research is being done to evaluate different BCCW treatment and disposal methods. One waste management option under consideration is reuse of BCCW in utility wet flue gas desulfurization (FGD) systems. To investigate this option, a series of laboratory tests were performed in which five different types of BCCW were added to the reaction tank of EPRI's bench-scale wet limestone FGD system. This paper presents the results and conclusions from this study.

Stohs, M.; Owens, D.R. (Radian Corp. (US)); Micheletti, W. (Electric Power Research Inst., Palo Alto, CA (USA))

1988-01-01T23:59:59.000Z

65

Production of manufactured aggregates from flue gas desulfurization by-products  

SciTech Connect

CONSOL R and D has developed a disk pelletization process to produce manufactured aggregates from the by-products of various technologies designed to reduce sulfur emissions produced from coal utilization. Aggregates have been produced from the by-products of the Coolside and LIMB sorbent injection, the fluidized-bed combustion (FBC), spray dryer absorption (SDA), and lime and limestone wet flue gas desulfurization (FGD) processes. The aggregates produced meet the general specifications for use as road aggregate in road construction and for use as lightweight aggregate in concrete masonry units. Small field demonstrations with 1200 lb to 5000 lb of manufactured aggregates were conducted using aggregates produced from FBC ash and lime wet FGD sludge in road construction and using aggregates made from SDA ash and lime wet FGD sludge to manufacture concrete blocks. The aggregates for this work were produced with a bench-scale (200--400 lb batch) unit. In 1999, CONSOL R and D constructed and operated a 500 lb/hr integrated, continuous pilot plant. A variety of aggregate products were produced from lime wet FGD sludge. The pilot plant test successfully demonstrated the continuous, integrated operation of the process. The pilot plant demonstration was a major step toward commercialization of manufactured aggregate production from FGD by-products. In this paper, progress made in the production of aggregates from dry FGD (Coolside, LIMB, SDA) and FBC by-products, and lime wet FGD sludge is discussed. The discussion covers bench-scale and pilot plant aggregate production and aggregate field demonstrations.

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

1999-07-01T23:59:59.000Z

66

Advanced Flue Gas Desulfurization (AFGD) Demonstration Project. Technical progress report No. 15, July 1, 1993--September 30, 1993  

Science Conference Proceedings (OSTI)

The goal of this project is to demonstrate that, by combining state-of-the-art technology, highly efficient plant operation and maintenance capabilities and by-product gypsum sales, significant reductions of SO{sub 2} emissions can be achieved at approximately one-half the life cycle cost of a conventional Flue Gas Desulfurization (FGD) system. Further, this emission reduction is achieved without generating solid waste and while minimizing liquid wastewater effluent. Basically, this project entails the design, construction and operation of a nominal 600 MWe AFGD facility to remove SO{sub 2} from coal-fired power plant flue gas at the Northern Indiana Public Service Company`s Bailly Generating Station.

Not Available

1994-08-01T23:59:59.000Z

67

Case Studies to Evaluate Flue Gas Desulfurization Wastewater Physical/Chemical Treatment Performance  

Science Conference Proceedings (OSTI)

This study focuses on physical/chemical wastewater treatment technologies used to remove trace metals from flue gas desulphurization (FGD) wastewater. The scope of this study includes FGD wastewater treatment for trace metals.BackgroundThe United States Environmental Protection Agency (EPA) is currently revising the Effluent Limitations Guidelines (ELGs) for the steam electric power generating industry. The Electric Power Research Institute (EPRI) provided ...

2013-12-23T23:59:59.000Z

68

Effects of Ammonia and Flue Gas Desulfurization (FGD) Wastewater on Power Plant Effluent Toxicity  

Science Conference Proceedings (OSTI)

The Clean Air Act Amendments and subsequently the Clean Air Interstate Rule and other state-level actions have resulted in implementation of a variety of technologies to reduce emissions of nitrogen oxides (NOx), and to further reduce emissions of sulfur oxides (SOx). Selective Catalytic Reduction (SCR) and SNCR (non-catalytic) are two of the primary NOx emission reduction technologies. Often, ammonia is injected into flue gas as the reductant for the chemical reaction that converts NOx to nitrogen gas. ...

2007-12-18T23:59:59.000Z

69

Management of dry flue gas desulfurization by-products in underground mines. Annual report, October 1994--September 1995  

SciTech Connect

On September 30, 1993, the U.S. 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 several technologies for the placement of coal combustion residues (CCBs) in abandoned coal mines, and will assess the environmental impact of such underground CCB placement. This report describes progress in the following areas: environmental characterization, mix development and geotechnical characterization, material handling and system economics, underground placement, and field demonstration.

Chugh, Y.P.; Dutta, D.; Esling, S. [and others

1995-10-01T23:59:59.000Z

70

The impact of wet flue gas desulfurization scrubbing on mercury emissions from coal-fired power stations  

Science Conference Proceedings (OSTI)

The article introduces a predictive capability for mercury (Hg) retention in any Ca-based wet flue gas desulfurization (FGD) scrubber, given Hg speciation at the FGD inlet, the flue gas composition, and the sulphur dioxide (SO{sub 2}) capture efficiency. A preliminary statistical analysis of data from 17 full-scale wet FGDs connects flue gas compositions, the extents of Hg oxidation at FGD inlets, and Hg retention efficiencies. These connections show that solution chemistry within the FGD determines Hg retention. A more thorough analysis based on thermochemical equilibrium yields highly accurate predictions for total Hg retention with no parameter adjustments. For the most reliable data, the predictions were within measurement uncertainties for both limestone and Mg/lime systems operating in both forced and natural oxidation mode. With the U.S. Environmental Protection Agency's (EPA) Information Collection Request (ICR) database, the quantitative performance was almost as good for the most modern FGDs, which probably conform to the very high SO{sub 2} absorption efficiencies assumed in the calculations. The large discrepancies for older FGDs are tentatively attributed to the unspecified SO{sub 2} capture efficiencies and operating temperatures and to the possible elimination of HCl in prescrubbers. The equilibrium calculations suggest that Hg retention is most sensitive to inlet HCl and O{sub 2} levels and the FGD temperature; weakly dependent on SO{sub 2} capture efficiency; and insensitive to HgCl{sub 2}, NO, CA:S ratio, slurry dilution level in limestone FGDs, and MgSO{sub 3} levels in Mg/lime systems. Consequently, systems with prescrubbers to eliminate HCl probably retain less Hg than fully integrated FGDs. The analysis also predicts re-emission of Hg{sub 0} but only for inlet O{sub 2} levels that are much lower than those in full-scale FGDs. 12 refs., 5 figs., 3 tabs.

Stephen Niksa; Naoki Fujiwara [Niksa Energy Associates, Belmont, CA (US)

2005-07-01T23:59:59.000Z

71

Flue Gas Desulfurization Gypsum Agricultural Network: Ohio Sites 1 (Mixed Hay) and 2 (Corn)  

Science Conference Proceedings (OSTI)

The objectives of this work conducted during 2008–2010 were to evaluate potential beneficial agricultural uses of flue gas desulphurization gypsum (FGDG) in eastern Ohio and to assess the potential for environmental effects of the use of FGDG. Two field experiments were conducted at the eastern Ohio research site, one involving a mixed-grass hay field and the other a corn (Zea mays L.) field. FGDG and mined gypsum product were applied one time at rates of 0.2, 2.0, and 20 megagrams ...

2012-09-17T23:59:59.000Z

72

Longer-term Characterization of Mercury Partitioning and Re-emissions in a Full-scale Wet Flue Gas Desulfurization System, Site 2  

Science Conference Proceedings (OSTI)

This document presents and discusses results from an EPRI project focused on understanding and enhancing how mercury is captured by a wet flue gas desulfurization (FGD) system and how it partitions among the FGD liquor, fine solids, and bulk FGD solid byproduct. A second objective was to close a mercury balance around the host unit by determining what portion of the coal mercury exits the stack with the scrubbed flue gas and how much ends up in the fly ash, byproduct gypsum, and FGD wastewater. During t...

2010-12-23T23:59:59.000Z

73

Selenium Removal by Iron Cementation from a Coal-Fired Power Plant Flue Gas Desulfurization Wastewater in a Continuous Flow System-- a Pilot Study  

Science Conference Proceedings (OSTI)

This technical update describes work funded by the Electric Power Research Institute (EPRI) and performed by MSE Technology Applications, Inc. (MSE) at a coal-fired power plant burning Powder River Basin (PRB) coal (identified in this report as Plant E). This work was based on encouraging results obtained during previous EPRI-funded work on flue gas desulfurization (FGD) wastewater treatability testing by MSE, which focused on selenium removal from a variety of FGD wastewater sources. The results from th...

2009-07-29T23:59:59.000Z

74

Pilot-Scale Demonstration of Hybrid Zero-Valent Iron Water Treatment Technology: Removing Trace Metals from Flue Gas Desulfurization (FGD) Wastewater  

Science Conference Proceedings (OSTI)

In previous laboratory- and field bench-scale tests, the hybrid zero-valent iron (hZVI) process had been demonstrated capable of removing selenium, mercury, nitrates, and other pollutants from flue gas desulfurization (FGD) wastewater. By incorporating zero-valent iron (ZVI) with magnetite and certain Fe(II) species, the hZVI technology creates a highly reactive mixture that can transform and immobilize various trace metals, oxyanions, and other impurities from aqueous streams. To further evaluate ...

2013-04-09T23:59:59.000Z

75

Management of dry flue gas desulfurization by-products in underground mines. Topical report, April 1, 1996--April 30, 1997  

Science Conference Proceedings (OSTI)

This report represents the Final Technical Progress Report for Phase II of the overall program for a cooperative research agreement between the U.S. Department of Energy - MORGANTOWN Energy Technology Center (DOE-METC) and Southern Illinois University at Carbondale (SIUC). Under the agreement, SIUC will develop and demonstrate technologies for the handling, transport, and placement in abandoned underground coal mines of dry flue gas desulfurization by-products, such as fly ash, scrubber sludge, fluidized bed combustion by-products, and will assess the environmental impact of such underground placement. The overall program is divided into three (3) phases. Phase II of the program is primarily concerned with developing and testing the hardware for the actual underground placement demonstrations. Two technologies have been identified and hardware procured for full-scale demonstrations: (1) hydraulic placement, where coal combustion by-products (CCBs) will be placed underground as a past-like mixture containing about 70 to 75 percent solids; and (2) pneumatic placement, where CCBs will be placed underground as a relatively dry material using compressed air. 42 refs., 36 figs., 36 tabs.

Chugh, Y.P.; Brackebusch, F.; Carpenter, J. [and others

1998-12-31T23:59:59.000Z

76

Economic assessment of advanced flue gas desulfurization processes. Final report. Volume 2. Appendices G, H, and I  

SciTech Connect

This report presents the results of a project sponsored by the Morgantown Energy Technology Center (METC). The purpose of the study was to perform an economic and market assessment of advanced flue gas desulfurization (FGD) processes for application to coal-fired electric utility plants. The time period considered in the study is 1981 through 1990, and costs are reported in 1980 dollars. The task was divided into the following four subtasks: (1) determine the factors affecting FGD cost evaluations; (2) select FGD processes to be cost-analyzed; (3) define the future electric utility FGD system market; and (4) perform cost analyses for the selected FGD processes. The study was initiated in September 1979, and separate reports were prepared for the first two subtasks. The results of the latter two subtasks appear only in this final report, since the end-date of those subtasks coincided with the end-date of the overall task. The Subtask 1 report, Criteria and Methods for Performing FGD Cost Evaluation, was completed in October 1980. A slightly modified and condensed version of that report appears as Appendix B to this report. The Subtask 2 report, FGD Candidate Process Selection, was completed in January 1981, and the principal outputs of that subtask appear in Appendices C and D to this report.

Bierman, G. R.; May, E. H.; Mirabelli, R. E.; Pow, C. N.; Scardino, C.; Wan, E. I.

1981-09-01T23:59:59.000Z

77

Management of dry flue gas desulfurization by-products in underground mines. Quarterly report, October--December 1994  

SciTech Connect

On September 30, 1993, the US Department of Energy, Morgantown Energy Technology Center and Southern Illinois University at Carbondale (SIUC) entered into a cooperative agreement entitled ``Management of Dry Flue Gas Desulfurization By-Products in Underground Mines`` (DE-FC21-93MC30252). Under the agreement, Southern Illinois University at Carbondale will develop and demonstrate several technologies for the placement of coal combustion residues in abandoned coal mines, and will assess the environmental impact of such underground residues placement. The major event during the quarter was the demonstration of the SEEC, Inc. technology for loading and transporting coal combustion residues in the SEEC developed Collapsible Intermodal Containers (CIC). The demonstration was held on November 17, 1994, at the Illinois Power Company Baldwin power plant, and was attended by about eighty (80) invited guest. Also during the quarter meetings were held with Peabody Coal Company officials to finalize the area in the Peabody No. 10 mine to be used for the placement of coal combustion residues. Work under the Materials Handling and Systems Economics area continued, particularly in refining the costs and systems configuration and in economic evaluation of various systems using equipment leasing rather than equipment purchases. Likewise, work progressed on residues characterization, with some preparations being made for long-term testing.

Chugh, Y.; Dutta, D.; Esling, S.; Ghafoori, N.; Paul, B.; Sevim, H.; Thomasson, E.

1995-01-01T23:59:59.000Z

78

Catalytic seawater flue gas desulfurization process: an experimental pilot plant study  

SciTech Connect

In previous articles by the authors on seawater S(IV) oxidation kinetics, a significant catalytic effect was demonstrated by means of a commercially available activated carbon. The aims of this study carried out at pilot plant scale were to assess the use of high-efficiency structured packing and to validate the positive results obtained previously in laboratory studies. A comparison between a packed tower and a spray column was made by maintaining the same desulfurization efficiency. A 47% reduction in seawater flow can be obtained with a packed tower. This option seems to be more economical, with a reduction in operation costs of least of 33%. With the appropriate activated carbon, it is possible to reach a greater oxidation rate at a low pH level than by operating conventionally at a high pH level without a catalyst. A preliminary technical and financial comparison between the advanced seawater desulfurization process (equipped with a packed tower and a catalytic oxidation plant) and the conventional process (spray tower and noncatalytic oxidation) was carried out. 18 refs., 4 figs., 4 tabs.

F. Vidal B.; P. Ollero; F.J. Gutierrez Ortiz; A. Villanueva [University of Seville, Seville (Spain). Department of Chemical and Environmental Engineering

2007-10-15T23:59:59.000Z

79

Pilot-Scale Demonstration of hZVI Process for Treating Flue Gas Desulfurization Wastewater at Plant Wansley, Carrollton, GA  

E-Print Network (OSTI)

The hybrid Zero Valent Iron (hZVI) process is a novel chemical treatment platform that has shown great potential in our previous bench-scale tests for removing selenium, mercury and other pollutants from Flue Gas Desulfurization (FGD) wastewater. This integrated treatment system employs new iron chemistry to create highly reactive mixture of Fe^0, iron oxides (FeOx) and various forms of Fe (II) for the chemical transformation and mineralization of various heavy metals in water. To further evaluate and develop the hZVI technology, a pilot-scale demonstration had been conducted to continuously treat 1-2 gpm of the FGD wastewater for five months at Plant Wansley, a coal-fired power plant of Georgia Power. This demonstrated that the scaled-up system was capable of reducing the total selenium (of which most was selenate) in the FGD wastewater from over 2500 ppb to below 10 ppb and total mercury from over 100 ppb to below 0.01 ppb. This hZVI system reduced other toxic metals like Arsenic (III and V), Chromium (VI), Cadmium (II), Lead (II) and Copper (II) from ppm level to ppb level in a very short reaction time. The chemical consumption was estimated to be approximately 0.2-0.4 kg of ZVI per 1 m^3 of FGD water treated, which suggested the process economics could be very competitive. The success of the pilot test shows that the system is scalable for commercial application. The operational experience and knowledge gained from this field test could provide guidance to further improvement of technology for full scale applications. The hZVI technology can be commercialized to provide a cost-effective and reliable solution to the FGD wastewater and other metal-contaminated waste streams in various industries. This technology has the potential to help industries meet the most stringent environmental regulations for heavy metals and nutrients in wastewater treatment.

Peddi, Phani 1987-

2011-12-01T23:59:59.000Z

80

Management of dry flue gas desulfurization by-products in underground mines. Quarterly technical progress report, April 1995--June 1995  

SciTech Connect

On September 30, 1993, the U.S. Department of Energy-Morgantown Energy Technology Center 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 several technologies for the placement of coal combustion residues in abandoned coal mines, and will assess the environmental impact of such underground residues placement. Previous quarterly Technical Progress Reports have set forth the specific objectives of the program, and a discussion of these is not repeated here. Rather, this report discusses the technical progress made during the period April 1 - June 30, 1995. A final topical report on the SEEC, Inc. demonstration of its technology for the transporting of coal combustion residues was completed during the quarter, although final printing of the report was accomplished early in July, 1995. The SEEC technology involves the use of Collapsible Intermodal Containers (CIC`s) developed by SEEC, and the transportation of such containers - filled with fly ash or other coal combustion residues - on rail coal cars or other transportation means. Copies of the final topical report, entitled {open_quotes}The Development and Testing of Collapsible Intermodal Containers for the Handling and Transport of Coal Combustion Residues{close_quotes} were furnished to the Morgantown Energy Technology Center. The Rapid Aging Test colums were placed in operation during the quarter. This test is to determine the long-term reaction of both the pneumatic and hydraulic mixtures to brine as a leaching material, and simulates the conditions that will be encountered in the actual underground placement of the coal combustion residues mixtures. The tests will continue for about one year.

Chugh, Y.P.; Dutta, D.; Esling, S. [and others

1995-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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.


81

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

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

82

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

Science Conference Proceedings (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

83

Full-Scale Testing of a Mercury Oxidation Catalyst Upstream of a Wet Flue Gas Desulfurization System  

Science Conference Proceedings (OSTI)

The objective of this project was to demonstrate at full scale the use of solid honeycomb catalysts to promote the oxidation of elemental mercury (Hg0) in flue gas from coal combustion. The project was conducted from July 24, 2006 through June 30, 2010. It was conducted with cofunding from the U.S. Department of Energy's National Energy Technology Laboratory as part of Cooperative Agreement DE-FC26-06NT42778, "Full-Scale Testing of a Mercury Oxidation Catalyst Upstream of a Wet FGD System." Private secto...

2010-08-31T23:59:59.000Z

84

High-volume, high-value usage of flue gas desulfurization (FGD) by-products in underground mines - Phase I: Laboratory investigations. Quarterly report, October 1993--December 1993  

SciTech Connect

This project proposes to use pneumatically or hydraulically emplaced dry-flue gas desulfurization (FGD) by-products to backfill the adits left by highwall mining. Backfilling highwall mine adits with dry-FGD materials is technically attractive. The use of an active highwall mine would allow the dry-FGD material to be brought in using the same transportation network used to move the coal out, eliminating the need to recreated the transportation infrastructure, thereby saving costs. Activities during the period included the negotiations leading to the final cooperative agreement for the project and the implementation of the necessary instruments at the University of Kentucky to administer the project. Early in the negotiations, a final agreement on a task structure was reached and a milestone plan was filed. A review was initiated of the original laboratory plan as presented in the proposal, and tentative modifications were developed. Selection of a mine site was made early; the Pleasant Valley mine in Greenup County was chosen. Several visits were made to the mine site to begin work on the hydrologic monitoring plan. The investigation of the types of permits needed to conduct the project was initiated. Considerations concerning the acceptance and implementation of technologies led to the choice of circulating fluidized bed ash as the primary material for the study. Finally, the membership of a Technical Advisory Committee for the study was assembled.

Not Available

1994-03-01T23:59:59.000Z

85

Management of dry flue gas desulfurization by-products in underground mines. Quarterly technical progress report, [October 1, 1993--December 31, 1993  

Science Conference Proceedings (OSTI)

The ``Management of Dry Flue Gas Desulfurization By-Products in Underground Mines`` program is one of the largest programs ever undertaken by the Mining Engineering Department of Southern Illinois university, both in terms of complexity and in terms of funding. Total funding over the expected four-year extent of the program, including both Department of Energy, matching Southern Illinois University funds, and contributed funds, this program exceeds three million dollars. The number of cooperating organizations adds to the management complexity of the program. It was believed, therefore, that sound management plan and management base is essential for the efficient and effective conduct of the program. This first quarter period (i.e., October 1--December 31, 1993) was developed to establishing the management base, developing a sound management plan, developing a test plan, and developing sound fiscal management and control. Actual technical operations, such as residue sample acquisition, residue analyses, groundwater sample acquisition and analyses, and material handling studies will get underway early in the next quarter (i.e., January 1--March 31, 1994). Some early results of residue analyses and groundwater analyses should be available by the end of the second quarter. These results will be reported in the next Technical Progress Report.

Thomasson, E.M.; Chugh, Y.P.; Esling, S.; Honaker, R.; Paul, B.; Sevin, H.

1994-01-01T23:59:59.000Z

86

Adsorption and desorption of sulfur dioxide on novel adsorbents for flue gas desulfurization. Final report, September 1, 1993--August 31, 1994  

SciTech Connect

Dry regenerative sorption processes have recently attracted increasing attention in flue gas desulfurization (FGD) because of their several advantages over the conventional wet-scrubbing processes. Dry sorbents are usually made by coating a transition or alkaline earth metal precursor on the surface of a porous support. Major disadvantages of these sorbents prepared by the conventional methods include relatively poor attrition resistance and low SO{sub 2} sorption capacity. The physical and especially chemical attrition (associated with the sulphation-oxidation-reduction cycles in the process) deteriorates the performance of the sorbents. The low SO{sub 2} sorption capacity is primarily due to the small surface area of the support. Materials with a high surface area are not used as the supports for FGD sorbents because these materials usually are not thermally stable at high temperatures. In the past year, the research supported by Ohio Coal Development Office was focused on synthesis and properties of sol-gel derived alumina and zeolite sorbents with improved properties for FGD. The sol-gel derived alumina has large surface area, mesopore size and excellent mechanical strength. Some alumina-free zeolites not only posses the basic properties required as a sorbent for FGD (hydrophobicity, thermal and chemical stability, mechanical strength) but also have extremely large surface area and selective surface chemistry. The major objectives of this research program were to synthesize the sol-gel derived sorbents and to explore the use of the zeolites either directly as adsorbents or as sorbent support for FGD. The research was aimed at developing novel FGD sorbents possessing better sorption equilibrium and kinetic properties and improved physical and chemical attrition resistance.

Lin, Y.S. [University of Cincinnati, Cincinnati, OH (United States)

1995-02-01T23:59:59.000Z

87

High-volume, high-value usage of flue gas desulfurization (FGD) by-products in underground mines: Phase 1 -- Laboratory investigations. Quarterly report, July--September 1995  

Science Conference Proceedings (OSTI)

Efforts primarily focused on Subtask 2.2, Chemical and Mineralogical Characterization and Subtask 4.3, Selection and Testing of Transport System. As part of Subtask 2.2, samples were collected from the Freeman United Crown Mine III FBC disposal facility representing a verity of ages and weathering. A laboratory scale transport system has been built at the CAER to evaluate the potential of pneumatic transport for flue gas desulfurization material (FGDM) emplacement and to provide essential data for the mine emplacement demonstration as part of the Subtask 4.3 effort. The system is modeled after shotcreting systems and has the advantage that the material can be remotely placed without the need for forms. The test program is focusing on determining the pneumatic conditions necessary to maximize the strength of the emplaced FGDM under anticipated mine curing conditions while minimizing dust formation. Work on Subtask 4.1, Mine Selection, also proceeded during the quarter. A new mine site, located in the south-central section of the Pikeville quadrangle, Pike County, Kentucky, was examined for the field study. The proposed fill site is in the Middle Pennsylvanian Breathitt Formation Middle Amburgy coal bed, a coal previously mined by Costain elsewhere on the property. Efforts on Subtask 4.2, Hydrologic Monitoring Plan, focused primarily on theoretical issues concerning the effects of the mining and backfill activity on the ground water and surface water due to uncertainties in the location of the final field site. There are three major concerns about the effects of the mining activity: changes in the ground water flow field, changes in ground water quality, and consequential induced changes on stream flow.

NONE

1996-01-01T23:59:59.000Z

88

DRY FLUE GAS CLEANING PROCESSES FOR ACHIEVING AIR POLLUTANT EMISSIONS  

E-Print Network (OSTI)

was mercury adsorption onto calcium sulfate (CaSO4), a byproduct of the flue gas desulfurization (FGD) wet., Powers K.W., and Pitoniak E.R. (2004) Method for Purifying Flue Gases from Combustion Sources. PatentCoupling of Advanced Oxidation and Adsorption Processes onto Silica-Titania Composites for Low

Columbia University

89

System of treating flue gas  

DOE Patents (OSTI)

A system is described for treating or cleaning incinerator flue gas containing acid gases and radioactive and fissionable contaminants. Flue gas and a quench solution are fed into a venturi and then tangentially into the lower portion of a receptacle for restricting volumetric content of the solution. The upper portion of the receptacle contains a scrub bed to further treat or clean the flue gas.

Ziegler, D.L.

1975-12-01T23:59:59.000Z

90

Cement Kiln Flue Gas Recovery Scrubber Project  

SciTech Connect

The Cement Kiln Flue Gas Recovery Scrubber Project was a technical success and demonstrated the following: CKD can be used successfully as the sole reagent for removing SO2 from cement kiln flue gas, with removal efficiencies of 90 percent or greater; Removal efficiencies for HCl and VOCs were approximately 98 percent and 70 percent, respectively; Particulate emissions were low, in the range of 0.005 to 0.007 grains/standard cubic foot; The treated CKD sorbent can be recycled to the kiln after its potassium content has been reduced in the scrubber, thereby avoiding the need for landfilling; The process can yield fertilizer-grade K2SO4, a saleable by-product; and Waste heat in the flue gas can provide the energy required for evaporation and crystallization in the by-product recovery operation. The demonstration program established the feasibility of using the Recovery Scrubber{trademark} for desulfurization of flue gas from cement kilns, with generally favorable economics, assuming tipping fees are available for disposal of ash from biomass combustion. The process appears to be suitable for commercial use on any type of cement kiln. EPA has ruled that CKD is a nonhazardous waste, provided the facility meets Performance Standards for the Management of CKD (U.S. Environmental Protection Agency 1999d). Therefore, regulatory drivers for the technology focus more on reduction of air pollutants and pollution prevention, rather than on treating CKD as a hazardous waste. Application of the Recovery Scrubbe{trademark} concept to other waste-disposal operations, where pollution and waste reductions are needed, appears promising.

National Energy Technology Laboratory

2001-11-30T23:59:59.000Z

91

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

92

Recovery of Water from Boiler Flue Gas  

SciTech Connect

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

93

Fundamental mechanisms in flue gas conditioning. Final report  

SciTech Connect

The US Department of Energy`s Pittsburgh Energy Technology Center (DOE/PETC) initiated this project as part of a program to study the control of fine particles from coal combustion. Our project focus was flue gas conditioning. Various conditioning processes have lowered operating costs and increased collection efficiency at utility particulate control devices. By improving fine particle collection, flue gas conditioning also helps to control the emission of toxic metals, which are concentrated in the fine particle fraction. By combining a review of pertinent literature, laboratory characterization of a variety of fine powders and ashes, pilot-scale studies of conditioning mechanisms, and field experiences, Southern Research Institute has been able to describe many of the key processes that account for the effects that conditioning can have on fine-particle collection. The overall goal of this research project was to explain the mechanisms by which various flue gas conditioning processes alter the performance of particulate control devices. Conditioning involves the modification of one or more of the parameters that determine the magnitude of the forces acting on the fly ash particles. Resistivity, chemistry, cohesivity, size distribution, and particle morphology are among the basic properties of fly ash that significantly influence fine particle collection. Modifications of particulate properties can result in improved or degraded control device performance. These modifications can be caused by (1) changes to the process design or operation that affect properties of the flue gas, (2) addition of particulate matter such as flue-gas desulfurization sorbents to the process effluent stream, (3) injection of reactive gases or liquids into the flue gas. We recommend that humidification be seriously considered as a flue gas conditioning option. 80 refs., 69 figs., 23 tabs.

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

1996-03-20T23:59:59.000Z

94

Optimization on Seawater Desulfurization Efficiency Based on LSSVM-GA  

Science Conference Proceedings (OSTI)

Seawater flue gas Desulfurization (SFGD) was adopted in many coal-fired power plants of littoral for its low cost and high desulfurization efficiency. Operating Parameters would seriously affect SFGD efficiency, the desulfurization efficiency can be ... Keywords: SFGD, desulfurization efficiency, LSSVM, GA, optimization

Liu Ding-ping; Li Xiao-wei

2010-10-01T23:59:59.000Z

95

Mercury Sorbent Delivery System for Flue Gas  

NLE Websites -- All DOE Office Websites (Extended Search)

(NETL) is seeking licensing partners interested in implementing United States Patent Number 7,494,632 entitled "Mercury Sorbent Delivery System for Flue Gas." Disclosed in...

96

Advanced Hot-Gas Desulfurization Sorbents  

Science Conference Proceedings (OSTI)

Integrated gasification combined cycle (IGCC) power systems are being advanced worldwide for generating electricity from coal due to their superior environmental performance, economics, and efficiency in comparison to conventional coal-based power plants. Hot gas cleanup offers the potential for higher plant thermal efficiencies and lower cost. A key subsystem of hot-gas cleanup is hot-gas desulfurization using regenerable sorbents. Sorbents based on zinc oxide are currently the leading candidates and are being developed for moving- and fluidized- bed reactor applications. Zinc oxide sorbents can effectively reduce the H{sub 2}S in coal gas to around 10 ppm levels and can be regenerated for multicycle operation. However, all current first-generation leading sorbents undergo significant loss of reactivity with cycling, as much as 50% or greater loss in only 25-50 cycles. Stability of the hot-gas desulfurization sorbent over 100`s of cycles is essential for improved IGCC economics over conventional power plants. This project aims to develop hot-gas cleanup sorbents for relatively lower temperature applications, 343 to 538{degrees}C with emphasis on the temperature range from 400 to 500{degrees}. Recent economic evaluations have indicated that the thermal efficiency of IGCC systems increases rapidly with the temperature of hot-gas cleanup up to 350{degrees}C and then very slowly as the temperature is increased further. This suggests that the temperature severity of the hot-gas cleanup devices can be reduced without significant loss of thermal efficiency. The objective of this study is to develop attrition-resistant advanced hot-gas desulfurization sorbents which show stable and high sulfidation reactivity at 343{degrees}C (650{degrees}F) to 538{degrees}C(1OOO{degrees}F) and regenerability at lower temperatures than leading first generation sorbents.

Jothimurugesan, K.; Gangwal, S.K.; Gupta, R.; Turk, B.S.

1997-07-01T23:59:59.000Z

97

The Effect of Water on Natural Gas Desulfurization by Adsorption  

Science Conference Proceedings (OSTI)

Oct 15, 2006 ... The Effect of Water on Natural Gas Desulfurization by Adsorption by Ambalavanan Jayaraman, Gokhan Alptekin, Margarita Dubovik, Robert ...

98

Enviropower hot gas desulfurization pilot  

SciTech Connect

The objectives of the project are to develop and demonstrate (1) hydrogen sulfide removal using regenerable zinc titanate sorbent in pressurized fluidized bed reactors, (2) recovery of the elemental sulfur from the tail-gas of the sorbent regenerator and (3) hot gas particulate removal system using ceramic candle filters. Results are presented on pilot plant design and testing and modeling efforts.

Ghazanfari, R.; Feher, G.; Konttinen, J.; Ghazanfari, R.; Lehtovaara, A.; Mojtahedi, W.

1994-11-01T23:59:59.000Z

99

Sorbent for use in hot gas desulfurization  

DOE Patents (OSTI)

A multiple metal oxide sorbent supported on a zeolite of substantially silicon oxide is used for the desulfurization of process gas streams, such as from a coal gasifier, at temperatures in the range of about 1200.degree. to about 1600.degree. F. The sorbent is provided by a mixture of copper oxide and manganese oxide and preferably such a mixture with molybdenum oxide. The manganese oxide and the molybdenum are believed to function as promoters for the reaction of hydrogen sulfide with copper oxide. Also, the manganese oxide inhibits the volatilization of the molybdenum oxide at the higher temperatures.

Gasper-Galvin, Lee D. (Washington, PA); Atimtay, Aysel T. (Cankaya, TR)

1993-01-01T23:59:59.000Z

100

Hot gas desulfurization sorbent and method  

DOE Patents (OSTI)

A multiple metal oxide sorbent supported on a zeolite of substantially silicon oxide is used for the desulfurization of process gas streams, such as from a coal gasifier, at temperatures in the range of about 1200{degrees} to about 1600{degrees}F. The sorbent is provided by a mixture of copper oxide and manganese oxide and preferably such a mixture with molybdenum oxide. The manganese oxide and the molybdenum are believed to function as promoters for the reaction of hydrogen sulfide with copper oxide. Also, the manganese oxide inhibits the volatilization of the molybdenum oxide at the higher temperatures.

Gasper-Galvin, L.D.; Atimtay, A.T.

1991-03-13T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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.


101

Hot gas desulfurization sorbent and method  

DOE Patents (OSTI)

A multiple metal oxide sorbent supported on a zeolite of substantially silicon oxide is used for the desulfurization of process gas streams, such as from a coal gasifier, at temperatures in the range of about 1200[degrees] to about 1600[degrees]F. The sorbent is provided by a mixture of copper oxide and manganese oxide and preferably such a mixture with molybdenum oxide. The manganese oxide and the molybdenum are believed to function as promoters for the reaction of hydrogen sulfide with copper oxide. Also, the manganese oxide inhibits the volatilization of the molybdenum oxide at the higher temperatures.

Gasper-Galvin, L.D.; Atimtay, A.T.

1991-03-13T23:59:59.000Z

102

EPRI Environmental Control Technology Center: FGD Wet Scrubber Performance At High Flue Gas Velocities  

Science Conference Proceedings (OSTI)

This report summarizes the impact of operating a wet flue gas desulfurization scrubber system at high flue gas velocities up to 20ft/sec (6.1 m/sec). It includes results for countercurrent spray, tray, and packing designs a variety of nozzle types. The report also describes the effect of adding dibasic acid and the impact of operation of state-of-the-art mist elimination systems. These results will be useful for planning compliance with SO2 emission regulations whether a new system is planned or addition...

1997-01-28T23:59:59.000Z

103

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

Science Conference Proceedings (OSTI)

Laboratory studies were conducted to investigate dry, regenerable, alkali carbonate-based sorbents for the capture of CO{sub 2} from power plant flue gas. Electrobalance, fixed-bed and fluid-bed reactors were used to examine both the CO{sub 2} capture and sorbent regeneration phases of the process. Sodium carbonate-based sorbents (calcined sodium bicarbonate and calcined trona) were the primary focus of the testing. Supported sodium carbonate and potassium carbonate sorbents were also tested. Sodium carbonate reacts with CO{sub 2} and water vapor contained in flue gas at temperatures between 60 and 80 C to form sodium bicarbonate, or an intermediate salt (Wegscheider's salt). Thermal regeneration of this sorbent produces an off-gas containing equal molar quantities of CO{sub 2} and H{sub 2}O. The low temperature range in which the carbonation reaction takes place is suited to treatment of coal-derived flue gases following wet flue gas desulfurization processes, but limits the concentration of water vapor which is an essential reactant in the carbonation reaction. Sorbent regeneration in an atmosphere of CO{sub 2} and water vapor can be carried out at a temperature of 160 C or higher. Pure CO{sub 2} suitable for use or sequestration is available after condensation of the H{sub 2}O. Flue gas contaminants such as SO{sub 2} react irreversibly with the sorbent so that upstream desulfurization will be required when sulfur-containing fossil fuels are used. Approximately 90% CO{sub 2} capture from a simulated flue gas was achieved during the early stages of fixed-bed reactor tests using a nominal carbonation temperature of 60 C. Effectively complete sorbent carbonation is possible when the fixed-bed test is carried out to completion. No decrease in sorbent activity was noted in a 15-cycle test using the above carbonation conditions coupled with regeneration in pure CO{sub 2} at 160 C. Fluidized-bed reactor tests of up to five cycles were conducted. Carbonation of sodium carbonate in these tests is initially very rapid and high degrees of removal are possible. The exothermic nature of the carbonation reaction resulted in a rise in bed temperature and subsequent decline in removal rate. Good temperature control, possibly through addition of supplemental water and evaporative cooling, appears to be the key to getting consistent carbon dioxide removal in a full-scale reactor system. The tendency of the alkali carbonate sorbents to cake on contact with liquid water complicates laboratory investigations as well as the design of larger scale systems. Also their low attrition resistance appears unsuitable for their use in dilute-phase transport reactor systems. Sodium and potassium carbonate have been incorporated in ceramic supports to obtain greater surface area and attrition resistance, using a laboratory spray dryer. The caking tendency is reduced and attrition resistance increased by supporting the sorbent. Supported sorbents with loading of up to 40 wt% sodium and potassium carbonate have been prepared and tested. These materials may improve the feasibility of large-scale CO{sub 2} capture systems based on short residence time dilute-phase transport reactor systems.

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

2004-11-01T23:59:59.000Z

104

Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents  

Science Conference Proceedings (OSTI)

Laboratory studies were conducted to investigate dry, regenerable, alkali carbonate-based sorbents for the capture of CO{sub 2} from power plant flue gas. Electrobalance, fixed-bed and fluid-bed reactors were used to examine both the CO{sub 2} capture and sorbent regeneration phases of the process. Sodium carbonate-based sorbents (calcined sodium bicarbonate and calcined trona) were the primary focus of the testing. Supported sodium carbonate and potassium carbonate sorbents were also tested. Sodium carbonate reacts with CO{sub 2} and water vapor contained in flue gas at temperatures between 60 and 80 C to form sodium bicarbonate, or an intermediate salt (Wegscheider's salt). Thermal regeneration of this sorbent produces an off-gas containing equal molar quantities of CO{sub 2} and H{sub 2}O. The low temperature range in which the carbonation reaction takes place is suited to treatment of coal-derived flue gases following wet flue gas desulfurization processes, but limits the concentration of water vapor which is an essential reactant in the carbonation reaction. Sorbent regeneration in an atmosphere of CO{sub 2} and water vapor can be carried out at a temperature of 160 C or higher. Pure CO{sub 2} suitable for use or sequestration is available after condensation of the H{sub 2}O. Flue gas contaminants such as SO{sub 2} react irreversibly with the sorbent so that upstream desulfurization will be required when sulfur-containing fossil fuels are used. Approximately 90% CO{sub 2} capture from a simulated flue gas was achieved during the early stages of fixed-bed reactor tests using a nominal carbonation temperature of 60 C. Effectively complete sorbent carbonation is possible when the fixed-bed test is carried out to completion. No decrease in sorbent activity was noted in a 15-cycle test using the above carbonation conditions coupled with regeneration in pure CO{sub 2} at 160 C. Fluidized-bed reactor tests of up to five cycles were conducted. Carbonation of sodium carbonate in these tests is initially very rapid and high degrees of removal are possible. The exothermic nature of the carbonation reaction resulted in a rise in bed temperature and subsequent decline in removal rate. Good temperature control, possibly through addition of supplemental water and evaporative cooling, appears to be the key to getting consistent carbon dioxide removal in a full-scale reactor system. The tendency of the alkali carbonate sorbents to cake on contact with liquid water complicates laboratory investigations as well as the design of larger scale systems. Also their low attrition resistance appears unsuitable for their use in dilute-phase transport reactor systems. Sodium and potassium carbonate have been incorporated in ceramic supports to obtain greater surface area and attrition resistance, using a laboratory spray dryer. The caking tendency is reduced and attrition resistance increased by supporting the sorbent. Supported sorbents with loading of up to 40 wt% sodium and potassium carbonate have been prepared and tested. These materials may improve the feasibility of large-scale CO{sub 2} capture systems based on short residence time dilute-phase transport reactor systems.

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

2004-09-30T23:59:59.000Z

105

Microbial reduction of SO{sub 2} and NO{sub x} as a means of by-product recovery/disposal from regenerable processes for the desulfurization of flue gas. Technical progress report, September 11, 1992--December 11, 1992  

DOE Green Energy (OSTI)

With the continual increase in the utilization of high sulfur and high nitrogen containing fossil fuels, the release of airborne pollutants into the environment has become a critical problem. The fuel sulfur is converted to SO{sub 2} during combustion. Fuel nitrogen and a fraction of the nitrogen from the combustion air are converted to nitric oxide and nitrogen dioxide, NO{sub x}. For the past five years Combustion Engineering (now Asea Brown Boveri or ABB) and, since 1986, the University of Tulsa (TU) have been investigating the oxidation of H{sub 2}S by the facultatively anaerobic and autotrophic bacterium Thiobacillus denitrificans and have developed a process, concept for the microbial removal of H{sub 2}S from a gas stream the simultaneous removal of SO{sub 2} and NO by D. desulfuricans and T. denitrificans co-cultures and cultures-in-series was demonstrated. These systems could not be sustained due to NO inhibition of D. desulfuricans. However, a preliminary economic analysis has shown that microbial reduction of SO{sub 2} to H{sub 2}S with subsequent conversion to elemental sulfur by the Claus process is both technically and economically feasible if a less expensive carbon and/or energy source can be found. It has also been demonstrated that T. denitrificans can be grown anaerobically on NO(g) as a terminal electron acceptor with reduction to elemental nitrogen. Microbial reduction of NO{sub x} is a viable process concept for the disposal of concentrated streams of NO{sub x} as may be produced by certain regenerable processes for the removal of SO{sub 2} and NO{sub x} from flue gas.

Sublette, K.L.

1992-12-31T23:59:59.000Z

106

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

E-Print Network (OSTI)

of Catalysts for Oxidation of Mercury in Flue Gas, Environ.mercury oxidation when the chlorine concentration in flue gas

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

2008-01-01T23:59:59.000Z

107

Recovery of Water from Boiler Flue Gas  

NLE Websites -- All DOE Office Websites (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.

108

Fundamental mechanisms in flue-gas conditioning  

Science Conference Proceedings (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 ash 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.

Dahlin, R.S.; Vann Bush, P.; Snyder, T.R.

1992-01-09T23:59:59.000Z

109

Fundamental mechanisms in flue gas conditioning  

Science Conference Proceedings (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

110

Induced Flue Gas Recirculation Performance Tests  

Science Conference Proceedings (OSTI)

Induced Flue Gas Recirculation (IFGR) is a proven, low-cost method for controlling NOx emissions on gas-fired utility boilers. In 1997, IFGR technology for power generation applications was first demonstrated at Entergy's Willow Glen station, near Baton Rouge, LA. Following the success with IFGR at Willow Glen, four members of the Gas/Oil Fired Boiler Performance and Combustion NOx Control Target (No.55 in 2000) installed, or plan to install, IFGR on an additional 27 units. American Electric Power has im...

2000-07-03T23:59:59.000Z

111

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), ...

112

Pilot Test of Bauxite Residue Carbonation With Flue Gas  

Science Conference Proceedings (OSTI)

... of bauxite residue in water with flue gas, produced from direct oil burning. ... New Development Model for Bauxite Deposits - Dedicated Compact Refinery.

113

Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents  

SciTech Connect

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

114

Catalysts for Oxidation of Mercury in Flue Gas  

NLE Websites -- All DOE Office Websites (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,

115

Development of advanced hot-gas desulfurization sorbents. Final report  

Science Conference Proceedings (OSTI)

The objective of this project was to develop hot-gas desulfurization sorbent formulations for relatively lower temperature application, with emphasis on the temperature range from 343--538 C. The candidate sorbents include highly dispersed mixed metal oxides of zinc, iron, copper, cobalt, nickel and molybdenum. The specific objective was to develop suitable sorbents, that would have high and stable surface area and are sufficiently reactive and regenerable at the relatively lower temperatures of interest in this work. Stability of surface area during regeneration was achieved by adding stabilizers. To prevent sulfation, catalyst additives that promote the light-off of the regeneration reaction at lower temperature was considered. Another objective of this study was to develop attrition-resistant advanced hot-gas desulfurization sorbents which show stable and high sulfidation reactivity at 343 to 538 C and regenerability at lower temperatures than leading first generation sorbents.

Jothimurugesan, K.; Adeyiga, A.A.; Gangwal, S.K.

1997-10-01T23:59:59.000Z

116

New process for coke-oven gas desulfurization  

SciTech Connect

With the EPA reclassifying spent iron oxide as a hazardous waste material in 1990, an alternative technology was sought for desulfurizing coke-oven gas. Vacasulf technology was adopted for reasons that included: producing of coke battery heating gas without further polishing and high-quality elemental sulfur; lowest operating cost in comparison with other methods; no waste products; and integrates with existing ammonia destruction facility. Vacasulf requires a single purchased material, potassium hydroxide, that reacts with carbon dioxide in coke-oven gas to form potassium carbonate which, in turn, absorbs hydrogen sulfide. Operation of the system has been successful following the resolution of relatively minor start-up problems.

Currey, J.H. [Citizens Gas and Coke Utility, Indianapolis, IN (United States)

1995-10-01T23:59:59.000Z

117

PRODUCTION OF CONSTRUCTION AGGREGATES FROM FLUE GAS DESULFURIZATION SLUDGE  

Science Conference Proceedings (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

118

THERMODYNAMIC DATA FOR FLUE-GAS DESULFURIZATION PROCESSES  

E-Print Network (OSTI)

of Energy, Div. of Fossil Energy, Report FE-2710-1, pg. 24 (by the Assistant Secretary for Fossil Energy, Office of Coalby the Assistant Secretary for Fossil Energy, Off1ce of Coal

Brewer, Leo

2013-01-01T23:59:59.000Z

119

THERMODYNAMIC DATA FOR FLUE-GAS DESULFURIZATION PROCESSES  

E-Print Network (OSTI)

De Carvalho, J. Chern. Thermodynamics D. Detry, J. Drowart,Vanderzee, J. Chern. Thermodynamics ! Q,lll3-36 (1978). (43)L.G. Hepler, J. Chern. Thermodynamics~~ (45) J.E. Desnoyers,

Brewer, Leo

2013-01-01T23:59:59.000Z

120

Flue Gas Desulfurization Bid Preparation and Proposal Review Guideline  

Science Conference Proceedings (OSTI)

The prospect of more stringent limits for sulfur dioxide (SO2) has led power producers to begin planning for the future installation of FGD systems to meet new emission limits for their power plants. Major activity has already begun with the announcements of system-wide FGD system installations by many utilities in the southeastern United States. Contractor selection is a critical component to the successful compliance with regulatory requirements. This document provides utilities with the tools that the...

2003-03-10T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

Inspection Guideline for Wet Flue Gas Desulfurization Systems  

Science Conference Proceedings (OSTI)

Severe corrosion attack has occurred in several absorber vessels constructed of duplex 2205 and 255 stainless steels. There are also mounting concerns that earlier generation absorber vessels fabricated with austenitic stainless steels may also be subject to underdeposit and pitting corrosion attack. This corrosion attack has been found in several of the spray tower/ tray tower and jet bubble reactor designs constructed of stainless steels and are reported to be occurring with relatively little service l...

2011-08-22T23:59:59.000Z

122

THERMODYNAMIC DATA FOR FLUE-GAS DESULFURIZATION PROCESSES  

E-Print Network (OSTI)

N.T. Ioffe, et. al. Thermodynamic Constants of Materials,Heats and Related Thermodynamic Quan- ti ties , John W i 1 eN.P.L. Computer Analysed Thermodynamic Data: Organic and

Brewer, Leo

2013-01-01T23:59:59.000Z

123

Desulfurized gas production from vertical kiln pyrolysis  

DOE Patents (OSTI)

A gas, formed as a product of a pyrolysis of oil shale, is passed through hot, retorted shale (containing at least partially decomposed calcium or magnesium carbonate) to essentially eliminate sulfur contaminants in the gas. Specifically, a single chambered pyrolysis vessel, having a pyrolysis zone and a retorted shale gas into the bottom of the retorted shale zone and cleaned product gas is withdrawn as hot product gas near the top of such zone.

Harris, Harry A. (Rifle, CO); Jones, Jr., John B. (Grand Junction, CO)

1978-05-30T23:59:59.000Z

124

Multi-component Removal in Flue Gas by Aqua Ammonia  

NLE Websites -- All DOE Office Websites (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.

125

Thief Process Removal of Mercury from Flue Gas  

NLE Websites -- All DOE Office Websites (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

126

CO2 Capture Membrane Process for Power Plant Flue Gas  

NLE Websites -- All DOE Office Websites (Extended Search)

Membrane Process for Power Plant Flue Gas Background The mission of the U.S. Department of Energy's (DOE) Existing Plants, Emissions & Capture (EPEC) Research and Development (R&D)...

127

Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents  

NLE Websites -- All DOE Office Websites (Extended Search)

Mill Road P.O. Box 10940 Pittsburgh, PA 15236 412-386-4966 jose.figueroa@netl.doe.gov Carbon DioxiDe Capture from flue Gas usinG Dry reGenerable sorbents Background Currently...

128

Industrial Plant for Flue Gas Treatment with High Power Electron Accelerators  

SciTech Connect

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.

Chmielewski, Andrzej G. [Institute of Nuclear Chemistry and Technology, Warsaw (Poland); University of technology, faculty of Process and Chemical Engineering, Warsaw (Poland); Tyminski, Bogdan; Zimek, Zbigniew; Pawelec, Andrzej [Institute of Nuclear Chemistry and Technology, Warsaw (Poland); Licki, Janusz [Institute of Atomic Energy, Swierk (Poland)

2003-08-26T23:59:59.000Z

129

Automatic flue gas heat recovery system  

Science Conference Proceedings (OSTI)

An automatic flue gas heat recovery system for supplementing or replacing a conventional, separate hot water system. In the example described, the heat recovery system is applied to a pizza restaurant where large quantities of heat energy are normally wasted up an oven chimney stack, and large quantities of hot water also are required for restaurant operations. An electric motor driven pump circulates water in a closed loop between a storage tank and a heat exchanger tube located in the oven chimney stack. A thermostat control automatically starts the pump when the oven heats the chimney stack to an effective water heating temperature. When temperature in the storage tank reaches a predetermined maximum, the thermostat control stops the pump, opens a drain valve, and dumps water quickly and completely from the heat exchanger tube. Three different embodiments are shown and described illustrating systems with one or more storage tanks and one or more pumps. In the plural storage tank embodiments, an existing hot water heating tank may be converted for use to augment a main tank supplied with the present system.

Whalen, D.A.

1983-02-22T23:59:59.000Z

130

Fundamental mechanisms in flue gas conditioning  

Science Conference Proceedings (OSTI)

This project is divided into four tasks. The Management Plan was developed in task 1. Task 2, Evaluation of Mechanisms in FGD Sorbent and Ash Interactions, focuses on the characteristics of binary mixtures of these distinct powders. Task 3, Evaluation of Mechanisms in Conditioning Agents and Ash, is designed to examine the effects of various conditioning agents on fine ash particles to determine the mechanisms by which these agents alter the physical properties of the ash. Tasks 2 and 3 began with an extensive literature search and the assembly of existing theories. This phase of the project is now complete. During the past quarter, initial preparations of laboratory equipment for laboratory testing have been made. A plan for initial laboratory tests has been submitted to the Project Manager for review. Laboratory testing will commence once these laboratory plans have been formally approved. The results of the work performed under task 2 and 3 will be included in a Flue Gas Conditioning Model that will be issued under task 4. The Final Report for the project will also be prepared under task 4.

Snyder, T.R.; Robinson, M.S.; Bush, P.V.

1992-04-27T23:59:59.000Z

131

Fundamental mechanisms in flue gas conditioning  

Science Conference Proceedings (OSTI)

This project is divided into four tasks. Task 1 is the Development of a Management Plan. Task 2, Evaluation of Mechanisms in FGD Sorbent and Ash Interactions, focuses on the characteristics of binary mixtures of these distinct powders. Task 3, Evaluation of Mechanisms in Conditioning Agents and Ash, is designed to examine the effects of various conditioning agents on fine ash particles to determine the mechanisms by which these agents alter the physical properties of the ash. Tasks 2 and 3 began with an extensive literature search and the assembly of existing theories. The results of the work performed under Tasks 2 and 3 will be included in a Flue Gas Conditioning Model that will be issued under Task 4. The Final Report for the project will also be prepared under Task 4. This quarterly report covers four months in order to synchronize the reporting periods for this project with US Government quarters. Work performed on the project during the past quarter consisted almost entirely of the review of literature pertaining to the objectives of Tasks 2 and 3. The primary results of that review are discussed at length in Topical Reports 1 and 2, submitted January 9, 1992. As a consequence of the work described in the topical reports, several of the project's Measures of Success that were described in the first quarterly report have been achieved. This quarterly report will discuss these achievements.

Snyder, T.R.

1992-01-23T23:59:59.000Z

132

Process for production desulfurized of synthesis gas  

DOE Patents (OSTI)

A process for the partial oxidation of a sulfur- and silicate-containing carbonaceous fuel to produce a synthesis gas with reduced sulfur content which comprises partially oxidizing said fuel at a temperature in the range of 1900.degree.-2600.degree. F. in the presence of a temperature moderator, an oxygen-containing gas and a sulfur capture additive which comprises a calcium-containing compound portion, a sodium-containing compound portion, and a fluoride-containing compound portion to produce a synthesis gas comprising H.sub.2 and CO with a reduced sulfur content and a molten slag which comprises (1) a sulfur-containing sodium-calcium-fluoride silicate phase; and (2) a sodium-calcium sulfide phase.

Wolfenbarger, James K. (Torrance, CA); Najjar, Mitri S. (Wappingers Falls, NY)

1993-01-01T23:59:59.000Z

133

Takahax-Hirohax process for coke oven gas desulfurization  

SciTech Connect

This paper describes the Takahax-Hirohax process to desulfurize coke oven gas and to produce an ammonium sulfate end product. A review is also made of current operating experience and recent technical developments. The Takahax-Hirohax process is extremely useful when the COG contains a suitable ammonia to sulfur ratio and when ammonium sulfate is a desirable end product. No contaminated effluent streams are emitted from the process. The process is simple, reliable, flexible, and responds easily to COG variations. 4 figures, 3 tables. (DP)

Gastwirth, H.; Miner, R.; Stengle, W.

1981-01-01T23:59:59.000Z

134

Impact of supplemental firing of tire-derived fuel (TDF) on mercury species and mercury capture with the advanced hybrid filter in a western subbituminous coal flue gas  

Science Conference Proceedings (OSTI)

Pilot-scale experimental studies were carried out to evaluate the impacts of cofiring tire-derived fuel and a western subbituminous coal on mercury species in flue gas. Mercury samples were collected at the inlet and outlet of the Advanced Hybrid filter to determine mercury concentrations in the flue gas with and without TDF cofiring, respectively. Cofiring of TDF with a subbituminous coal had a significant effect on mercury speciation in the flue gas. With 100% coal firing, there was only 16.8% oxidized mercury in the flue gas compared to 47.7% when 5% TDF (mass basis) was fired and 84.8% when 10% TDF was cofired. The significantly enhanced mercury oxidation may be the result of additional homogeneous gas reactions between Hg{sup 0} and the reactive chlorine generated in the TDF-cofiring flue gas and the in situ improved reactivity of unburned carbon in ash by the reactive chlorine species. Although the cofiring of TDF demonstrated limited improvement on mercury-emission control with the Advanced Hybrid filter, it proved to be a very cost-effective mercury control approach for power plants equipped with wet or dry flue gas desulfurization (FGD) systems because of the enhanced mercury oxidation. 15 refs., 4 figs., 4 tabs.

Ye Zhuang; Stanley J. Miller [University of North Dakota, Grand Forks, ND (United States). Energy & Environmental Research Center

2006-05-15T23:59:59.000Z

135

Pilot-Scale and Full-Scale Evaluation of Treatment Technologies for the Removal of Mercury and Selenium in Flue Gas Desulphurization Water  

Science Conference Proceedings (OSTI)

This report presents an overall evaluation of the various advanced treatment technologies that the Electric Power Research Institute (EPRI) has tested for removal of mercury and selenium from flue gas desulfurization (FGD) water. EPRI conducted a literature survey followed by a preliminary laboratory-scale evaluation to screen promising technologies. For the technologies that were selected based on the success of laboratory-scale testing, EPRI worked with treatment vendors to further evaluate these techn...

2010-05-11T23:59:59.000Z

136

BENCH-SCALE DEMONSTRATION OF HOT-GAS DESULFURIZATION TECHNOLOGY  

SciTech Connect

The U.S. Department of Energy (DOE), Federal Energy Technology Center (FETC), is sponsoring research in advanced methods for controlling contaminants in hot coal gasifier gas (coal-derived fuel-gas) streams of integrated gasification combined-cycle (IGCC) power systems. The hot gas cleanup work seeks to eliminate the need for expensive heat recovery equipment, reduce efficiency losses due to quenching, and minimize wastewater treatment costs. Hot-gas desulfurization research has focused on regenerable mixed-metal oxide sorbents that can reduce the sulfur in coal-derived fuel-gas to less than 20 ppmv and can be regenerated in a cyclic manner with air for multicycle operation. Zinc titanate (Zn{sub 2} TiO{sub 4} or ZnTiO{sub 3}), formed by a solid-state reaction of zinc oxide (ZnO) and titanium dioxide (TiO{sub 2}), is currently one of the leading sorbents. Overall chemical reactions with Zn{sub 2} TiO{sub 4} during the desulfurization (sulfidation)-regeneration cycle are shown below: Sulfidation: Zn{sub 2} TiO{sub 4} + 2H{sub 2}S {yields} 2ZnS + TiO{sub 2} + 2H{sub 2}O; Regeneration: 2ZnS + TiO{sub 2} + 3O{sub 2} {yields} Zn{sub 2} TiO{sub 4} + 2SO{sub 2} The sulfidation/regeneration cycle can be carried out in a fixed-bed, moving-bed, or fluidized-bed reactor configuration. The fluidized-bed reactor configuration is most attractive because of several potential advantages including faster kinetics and the ability to handle the highly exothermic regeneration to produce a regeneration offgas containing a constant concentration of SO{sub 2}.

Unknown

1999-10-01T23:59:59.000Z

137

Flue Gas Conditioning Trial at Rochester Gas and Electric Russell Station  

Science Conference Proceedings (OSTI)

This report presents data and results of a full-scale evaluation of two flue gas conditioning agents considered as upgrades for the existing electrostatic precipitators (ESPs) at Rochester Gas and Electric's (RG&E) Russell Station. The flue gas additives evaluated were anhydrous ammonia and a proprietary chemical agent, ADA-23.

1999-04-06T23:59:59.000Z

138

Flue gas injection control of silica in cooling towers.  

Science Conference Proceedings (OSTI)

Injection of CO{sub 2}-laden flue gas can decrease the potential for silica and calcite scale formation in cooling tower blowdown by lowering solution pH to decrease equilibrium calcite solubility and kinetic rates of silica polymerization. Flue gas injection might best inhibit scale formation in power plant cooling towers that use impaired makeup waters - for example, groundwaters that contain relatively high levels of calcium, alkalinity, and silica. Groundwaters brought to the surface for cooling will degas CO{sub 2} and increase their pH by 1-2 units, possibly precipitating calcite in the process. Recarbonation with flue gas can lower the pHs of these fluids back to roughly their initial pH. Flue gas carbonation probably cannot lower pHs to much below pH 6 because the pHs of impaired waters, once outgassed at the surface, are likely to be relatively alkaline. Silica polymerization to form scale occurs most rapidly at pH {approx} 8.3 at 25 C; polymerization is slower at higher and lower pH. pH 7 fluids containing {approx}220 ppm SiO{sub 2} require > 180 hours equilibration to begin forming scale whereas at pH 8.3 scale formation is complete within 36 hours. Flue gas injection that lowers pHs to {approx} 7 should allow substantially higher concentration factors. Periodic cycling to lower recoveries - hence lower silica concentrations - might be required though. Higher concentration factors enabled by flue gas injection should decrease concentrate volumes and disposal costs by roughly half.

Brady, Patrick Vane; Anderson, Howard L., Jr.; Altman, Susan Jeanne

2011-06-01T23:59:59.000Z

139

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

140

Liquefaction and desulfurization of coal using synthesis gas  

DOE Patents (OSTI)

A process for desulfurizing and liquefying coal by heating said coal at a temperature of 375.degree.-475.degree. C in the presence of a slurry liquid, hydrogen, carbon monoxide, steam, and a catalyst comprising a desulfurization catalyst and an alkali metal salt.

Fu, Yuan C. (Bethel Park, PA)

1977-03-08T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

Kinetics of hot-gas desulfurization sorbents for transport reactors  

DOE Green Energy (OSTI)

Hot-gas desulfurization for the integrated gasification combined cycle (IGCC) process has been investigated by many researchers to remove effectively hydrogen sulfide with various metal oxide sorbents at elevated temperatures. Various metal oxide sorbents are formulated with metal oxides such as Fe, Co, Zn, and Ti. Initial reaction kinetics of formulated sorbents with hydrogen sulfide is studied in the presence of various amounts of moisture and hydrogen at various reaction temperatures. The objectives of this research are to study initial reaction kinetics for a sorbent-hydrogen sulfide heterogeneous reaction system, to investigate effects of concentrations of hydrogen sulfide, hydrogen, and moisture on dynamic absorption of H{sub 2}S into sorbents, to understand effects of space time of reaction gas mixtures on initial reaction kinetics of the sorbent-hydrogen sulfide system, and to evaluate effects of temperature and sorbent amounts on dynamic absorption of H{sub 2}S into sorbents. Experimental data on initial reaction kinetics of hydrogen sulfide with metal oxide sorbents were obtained with a 0.83-cm{sup 3} differential reactor. The reactivity of MCRH-67 sorbent and AHI-1 was examined. These sorbents were obtained from the Research Triangle Institute (RTI). The sorbents in the form of 70 {micro}m particles are reacted with 1,000--4,000 ppm hydrogen sulfide at 450--600 C. The range of space time of reaction gas mixtures is 0.03--0.09 s. The range of reaction duration is 4--14,400 s.

K.C. Kwon

2000-01-01T23:59:59.000Z

142

DEVELOPMENT OF ADVANCED HOT-GAS DESULFURIZATION PROCESSES  

Science Conference Proceedings (OSTI)

The techniques employed in this project have successfully demonstrated the feasibility of preparing sorbents that achieve greater than 99% H{sub 2}S removal at temperatures 480 C and that retain their activity over 50 cycles. Fundamental understanding of phenomena leading to chemical deactivation and high regeneration light-off temperature has enabled us to successfully prepare and scale up a FHR-32 sorbent that showed no loss in reactivity and capacity over 50 cycles. This sorbent removed H{sub 2}S below 80 ppmv and lighted-off nicely at 480 C during regeneration. Overall the test is a success with potential for an optimized FHR-32 to be a candidate for Sierra-Pacific. An advanced attrition resistant hot-gas desulfurization sorbent that can eliminate the problematic SO{sub 2} tail gas and yield elemental sulfur directly has been developed. Attrition resistant Zn-Fe sorbent (AHI-2) formulations have been prepared that can remove H{sub 2}S to below 20 ppmv from coal gas and can be regenerated using SO{sub 2} to produce elemental sulfur.

K. Jothimurugesan; Santosh K. Gangwal

2000-12-01T23:59:59.000Z

143

ISSN 1537-744X; doi:10.1100/2011/756264 Measurement of Mercury in Flue Gas Based on an Aluminum Matrix Sorbent  

E-Print Network (OSTI)

The measurement of total mercury in flue gas based on an economical aluminum matrix sorbent was developed in this paper. A sorbent trap consisted of three tubes was employed to capture Hg from flue gas. Hg trapped on sorbent was transferred into solution by acid leaching and then detected by CVAAS. Hg adsorbed on sorbent was recovered completely by leaching process. The 87.7 % recovery of Hg in flue gas by tube 1 and tube 2 was obtained on the equipment of coal combustion and sampling in lab. In order to evaluate the ability to recover and accurately quantify Hg 0 on the sorbent media, the analytical bias test on tube 3 spiked with Hg 0 was also performed and got the average recovery of 97.1%. Mercury measurements based on this method were conducted for three coal-fired power plants in China. The mercury in coal is distributed into bottom ash, electrostatic precipitator (ESP) ash, wet flue gas desulfurization (WFGD) reactant, and flue gas, and the relative distribution varied depending on factors such as the coal type and the operation conditions of plants. The mercury mass balances of three plants were also calculated which were 91.6%, 77.1%, and 118%, respectively. The reliability of this method was verified by the Ontario Hydro (OH) method either in lab or in field.

Juan Wang; Wei Xu; Xiaohao Wang; Wenhua Wang

2011-01-01T23:59:59.000Z

144

Method for enhancing the desulfurization of hot coal gas in a fluid-bed coal gasifier  

DOE Patents (OSTI)

A process and apparatus for providing additional desulfurization of the hot gas produced in a fluid-bed coal gasifier, within the gasifier. A fluid-bed of iron oxide is located inside the gasifier above the gasification bed in a fluid-bed coal gasifier in which in-bed desulfurization by lime/limestone takes place. The product gases leave the gasification bed typically at 1600.degree. to 1800.degree. F. and are partially quenched with water to 1000.degree. to 1200.degree. F. before entering the iron oxide bed. The iron oxide bed provides additional desulfurization beyond that provided by the lime/limestone.

Grindley, Thomas (Morgantown, WV)

1989-01-01T23:59:59.000Z

145

KINETICS OF HOT-GAS DESULFURIZATION SORBENTS FOR TRANSPORT REACTORS  

SciTech Connect

Hot-gas desulfurization for the integrated gasification combined cycle (IGCC) process has been investigated by many researchers to remove effectively hydrogen sulfide with various metal oxide sorbents at elevated temperatures. Various metal oxide sorbents are formulated with metal oxides such as Fe, Co, Zn, and Ti. Initial reaction kinetics of formulated sorbents with hydrogen sulfide is studied in the presence of various amounts of moisture and hydrogen at various reaction temperatures. The objectives of this research are to study initial reaction kinetics for a sorbent-hydrogen sulfide heterogeneous reaction system, to investigate effects of concentrations of hydrogen sulfide, hydrogen, and moisture on dynamic absorption of H{sub 2}S into sorbents, and to evaluate effects of temperature and sorbent amounts on dynamic absorption of H{sub 2}S into sorbents. Experimental data on initial reaction kinetics of hydrogen sulfide with metal oxide sorbents were obtained with a 0.83-cm{sup 3} differential reactor. The reactivity of MCRH-67 was examined in this report. This sorbent was obtained from the Research Triangle Institute (RTI). The sorbent in the form of 130 mm particles are reacted with 18000-ppm hydrogen sulfide at 350-525 C. The range of space time of reaction gas mixtures is 0.069-0.088 s. The range of reaction duration is 4-180 s.

K.C. Kwon

2002-01-01T23:59:59.000Z

146

KINETICS OF HOT-GAS DESULFURIZATION SORBENTS FOR TRANSPORT REACTORS  

DOE Green Energy (OSTI)

Hot-gas desulfurization for the integrated gasification combined cycle (IGCC) process has been investigated by many researchers to remove effectively hydrogen sulfide with various metal oxide sorbents at elevated temperatures. Various metal oxide sorbents are formulated with metal oxides such as Fe, Co, Zn, and Ti. Initial reaction kinetics of formulated sorbents with hydrogen sulfide is studied in the presence of various amounts of moisture and hydrogen at various reaction temperatures. The objectives of this research are to study initial reaction kinetics for a sorbent-hydrogen sulfide heterogeneous reaction system, to investigate effects of concentrations of hydrogen sulfide, hydrogen, and moisture on dynamic absorption of H{sub 2}S into sorbents, and to evaluate effects of temperature and sorbent amounts on dynamic absorption of H{sub 2}S into sorbents. Experimental data on initial reaction kinetics of hydrogen sulfide with metal oxide sorbents were obtained with a 0.83-cm{sup 3} differential reactor. The reactivity of EX-SO3 was examined in this report. This sorbent was obtained from the Research Triangle Institute (RTI). The sorbent in the form of 110 {micro}m particles are reacted with 18000-ppm hydrogen sulfide at 350-550 C. The range of space time of reaction gas mixtures is 0.069-0.088 s. The range of reaction duration is 4-180 s.

K.C. Kwon

2003-02-01T23:59:59.000Z

147

KINETICS OF HOT-GAS DESULFURIZATION SORBENTS FOR TRANSPORT REACTORS  

DOE Green Energy (OSTI)

Hot-gas desulfurization for the integrated gasification combined cycle (IGCC) process has been investigated by many researchers to remove effectively hydrogen sulfide with various metal oxide sorbents at elevated temperatures. Various metal oxide sorbents are formulated with metal oxides such as Fe, Co, Zn, and Ti. Initial reaction kinetics of formulated sorbents with hydrogen sulfide is studied in the presence of various amounts of moisture and hydrogen at various reaction temperatures. The objectives of this research are to study initial reaction kinetics for a sorbent-hydrogen sulfide heterogeneous reaction system, to investigate effects of concentrations of hydrogen sulfide, hydrogen, and moisture on dynamic absorption of H{sub 2}S into sorbents, and to evaluate effects of temperature and sorbent amounts on dynamic absorption of H{sub 2}S into sorbents. Experimental data on initial reaction kinetics of hydrogen sulfide with metal oxide sorbents were obtained with a 0.83-cm{sup 3} differential reactor. In this report, the reactivity of AHI-5 was examined. This sorbent was obtained from the Research Triangle Institute (RTI). The sorbent in the form of 70 {micro}m particles are reacted with 9000-18000 ppm hydrogen sulfide at 350-500 C. The range of space time of reaction gas mixtures is 0.071-0.088 s. The range of reaction duration is 4-10800 s.

K.C. Kwon

2001-01-01T23:59:59.000Z

148

SCALE-UP OF ADVANCED HOT-GAS DESULFURIZATION SORBENTS  

Science Conference Proceedings (OSTI)

The objective of this study was to develop advanced regenerable sorbents for hot gas desulfurization in IGCC systems. The specific objective was to develop durable advanced sorbents that demonstrate a strong resistance to attrition and chemical deactivation, and high sulfidation activity at temperatures as low as 343 C (650 F). Twenty sorbents were synthesized in this work. Details of the preparation technique and the formulations are proprietary, pending a patent application, thus no details regarding the technique are divulged in this report. Sulfidations were conducted with a simulated gas containing (vol %) 10 H{sub 2}, 15 CO, 5 CO{sub 2}, 0.4-1 H{sub 2}S, 15 H{sub 2}O, and balance N{sub 2} in the temperature range of 343-538 C. Regenerations were conducted at temperatures in the range of 400-600 C with air-N{sub 2} mixtures. To prevent sulfation, catalyst additives were investigated that promote regeneration at lower temperatures. Characterization were performed for fresh, sulfided and regenerated sorbents.

K. JOTHIMURUGESAN; S.K. GANGWAL

1998-03-01T23:59:59.000Z

149

Scale-Up of Advanced Hot-Gas desulfurization Sorbents.  

SciTech Connect

The overall objective of this project is to develop regenerable sorbents for hot gas desulfurization in IGCC systems. The specific objective of the project is to develop durable advanced sorbents that demonstrate a strong resistance to attrition and chemical deactivation, and high activity at temperatures as low as 343 {degrees}C (650{degrees}F). A number of formulations will be prepared and screened in a one-half inch fixed bed reactor at high pressure (1 to 20 atm) and high temperatures using simulated coal-derived fuel- gases. Screening criteria will include chemical reactivity, stability, and regenerability over the temperature range of 343{degrees}C to 650{degrees}C. After initial screening, at least 3 promising formulations will be tested for 25-30 cycles of absorption and regeneration. One of the superior formulations with the best cyclic performance will be selected for investigating scale up parameters. The scaled-up formulation will be tested for long term durability and chemical reactivity.

Jothimurugesan, K.; Gangwal, S.K.

1997-10-02T23:59:59.000Z

150

METC fluid-bed hot-gas desulfurization PDU  

SciTech Connect

METC is constructing an on-site, hot-gas desulfurization (HGD) process development unit (PDU) to support the US Department of Energy`s (DOE`s) Integrated Gasification Combined Cycle (IGCC) power systems program. With industrial participation, this PDU will be used for the further development of fluid-bed and transport reactor HGD configurations. The fluid-bed absorber and regenerator in the PDU were designed to operate in a turbulent as well as a bubbling regime. In addition, when encouraging results from a small-scale transport reactor unit became known, the decision was made to incorporate transport reactor provisions on both the sulfidation and regeneration sides of the PDU. With completion of National Environmental Policy Act (NEPA) documentation requirements, the preliminary process and equipment design, and the April groundbreaking to prepare the project site, the project is now proceeding at a faster, more visible pace. Equipment installation should be completed in about 2 years. This report describes the project.

Bissett, L.A.

1994-10-01T23:59:59.000Z

151

Scale-Up of Advanced Hot-Gas Desulfurization Sorbents  

Science Conference Proceedings (OSTI)

The overall objective of this project is to develop regenerable sorbents for hot gas desulfurization in IGCC systems. The specific objective of the project is to develop durable advanced sorbents that demonstrate a strong resistance to attrition and chemical deactivation, and high activity at temperatures as low as 343{degrees}C (650{degrees}F). A number of formulations will be prepared and screened in a 1/2-inch fixed bed reactor at high pressure (1 to 20 atm) and high temperatures using simulated coal-derived fuel-gases. Screening criteria will include, chemical reactivity, stability, and regenerability over the temperature range of 343{degrees}C to 650{degrees}C. After initial screening, at least 3 promising formulations will be tested for 25-30 cycles of absorption and regeneration. One of the superior formulations with the best cyclic performance will be selected for investigating scale up parameters. The scaled-up formulation will be tested for long term durability and chemical reactivity.

Jothimurugesan, K.; Gangwal, S.K.

1997-04-21T23:59:59.000Z

152

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

Science Conference Proceedings (OSTI)

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

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

2005-01-01T23:59:59.000Z

153

Flue gas conditioning for improved particle collection in electrostatic precipitators  

SciTech Connect

The purpose of this research program is to identify and evaluate a variety of additives capable of increasing particle cohesion which could be used for improving collection efficiency in an ESP. A three-phase screening process will be used to provide the, evaluation of many additives in a logical and cost-effective manner. The three step approach involves the following experimental setups: 1. Provide a preliminary screening in the laboratory by measuring the effects of various conditioning agents on reentrainment of flyash particles in an electric field operating at simulated flue gas conditions. 2. Evaluate the successful additives using a 100 acfm bench-scale ESP operating on actual flue gas. 3. Obtain the data required for scaling up the technology by testing the two or three most promising conditioning agents at the pilot scale.

Durham, M.D.

1992-04-27T23:59:59.000Z

154

CO2 Capture Membrane Process for Power Plant Flue Gas  

NLE Websites -- All DOE Office Websites (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

155

Biominetic Membrane for Co2 Capture from Flue Gas  

NLE Websites -- All DOE Office Websites (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

156

The Thief Process for Mercury Removal from Flue Gas  

E-Print Network (OSTI)

The Thief Process is a cost-effective variation to activated carbon injection (ACI) for removal of mercury from flue gas. In this scheme, partially combusted coal from the furnace of a pulverized coal power generation plant is extracted by a lance and then re-injected into the ductwork downstream of the air preheater. Recent results on a 500-lb/hr pilot-scale combustion facility show similar removals of mercury for both the Thief Process and ACI. The tests conducted to date at laboratory, bench, and pilot-scales demonstrate that the Thief sorbents exhibit capacities for mercury from flue gas streams that are comparable to those exhibited by commercially available activated carbons. Independent verification of the sorbent activity at a pilot-plant that uses a slipstream from a Wisconsin utility has been accomplished. A patent for the process was issued in February 2003 [1]. The Thief sorbents are cheaper than commerciallyavailable activated carbons; exhibit excellent capacities for mercury; and the overall process holds great potential for reducing the cost of mercury removal from flue gas [1-4].

Evan J. Granite; Mark C. Freeman; Richard A. Hargis; William J. O’dowd; Henry W. Pennline

2004-01-01T23:59:59.000Z

157

Development of advanced hot-gas desulfurization processes  

SciTech Connect

Advanced integrated gasification combined cycle (IGCC) power plants nearing completion, such as Sierra-Pacific, employ a circulating fluidized-bed (transport) reactor hot-gas desulfurization (HGD) process that uses 70-180 {micro}m average particle size (aps) zinc-based mixed-metal oxide sorbent for removing H{sub 2}S from coal gas down to less than 20 ppmv. The sorbent undergoes cycles of absorption (sulfidation) and air regeneration. The key barrier issues associated with a fluidized-bed HGD process are chemical degradation, physical attrition, high regeneration light-off (initiation) temperature, and high cost of the sorbent. Another inherent complication in all air-regeneration-based HGD processes is the disposal of the problematic dilute SO{sub 2} containing regeneration tail-gas. Direct Sulfur Recovery Process (DSRP), a leading first generation technology, efficiently reduces this SO{sub 2} to desirable elemental sulfur, but requires the use of 1-3 % of the coal gas, thus resulting in an energy penalty to the plant. Advanced second-generation processes are under development that can reduce this energy penalty by modifying the sorbent so that it could be directly regenerated to elemental sulfur. The objective of this research is to support the near and long term DOE efforts to commercialize the IGCC-HGD process technology. Specifically we aim to develop: optimized low-cost sorbent materials with 70-80 {micro}m average aps meeting all Sierra specs; attrition resistant sorbents with 170 {micro}m aps that allow greater flexibility in the choice of the type of fluidized-bed reactor e.g. they allow increased throughput in a bubbling-bed reactor; and modified fluidizable sorbent materials that can be regenerated to produce elemental sulfur directly with minimal or no use of coal gas. The effort during the reporting period has been devoted to testing the FHR-32 sorbent. FHR-32 sorbent was tested for 50 cycles of sulfidation in a laboratory scale reactor.

Jothimurugesan, K.

2000-04-17T23:59:59.000Z

158

Coke oven gas desulfurization: at Republic Steel's New Coking Facility, Warren, OH  

SciTech Connect

Our performance test indicates that the Sulfiban process is an effective method for removing H/sub 2/S from coke-oven gas. The process is able to handle variations in coke-oven gas flow and composition. Continuing efforts are underway to maintain optimum desulfurization conditions while trying to reduce waste production and MEA consumption. The problems which have prevented us from operating continuously have given us a better understanding of the process. This has contributed to better plant operations and greater equipment reliability for us to obtain continuous coke-oven gas desulfurization. 2 figures, 1 table.

Boak, S.C.; Prucha, D.G.; Turic, H.L.

1981-01-01T23:59:59.000Z

159

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

160

FUNDAMENTALS OF MERCURY OXIDATION IN FLUE GAS  

Science Conference Proceedings (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 two experimental scales and a modeling effort. The team is comprised of University of Utah, Reaction Engineering International, and 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 studies include HCl, NOx, and SO{sub 2} concentrations, ash constituents, and temperature. This report summarizes Year 1 results for the experimental and modeling tasks. Experiments in the drop tube are just beginning and a new, speciated mercury analyzer is up and running. A preliminary assessment has been made for the drop tube experiments using the existing model of gas-phase kinetics.

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

2004-08-01T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

Comparison of Furnace Flue Gas Temperature Monitors  

Science Conference Proceedings (OSTI)

This report summarizes the results of a temperature monitor comparison study performed at Ameren Sioux Station, in Missouri. The study compared the accuracy and ease of use of two radiation-based monitors, an Infra-View and SpectraTemp, and a newer tunable-diode laser (TDL) absorption-based device, the LTS-100. The instruments, installed in the upper furnace and allowed to run continuously for approximately 8 weeks, monitored and recorded exit gas temperatures during normal boiler operation and one brief...

2006-09-22T23:59:59.000Z

162

Water Extraction from Coal-Fired Power Plant Flue Gas  

Science Conference Proceedings (OSTI)

The overall objective of this program was to develop a liquid disiccant-based flue gas dehydration process technology to reduce water consumption in coal-fired power plants. The specific objective of the program was to generate sufficient subscale test data and conceptual commercial power plant evaluations to assess process feasibility and merits for commercialization. Currently, coal-fired power plants require access to water sources outside the power plant for several aspects of their operation in addition to steam cycle condensation and process cooling needs. At the present time, there is no practiced method of extracting the usually abundant water found in the power plant stack gas. This project demonstrated the feasibility and merits of a liquid desiccant-based process that can efficiently and economically remove water vapor from the flue gas of fossil fuel-fired power plants to be recycled for in-plant use or exported for clean water conservation. After an extensive literature review, a survey of the available physical and chemical property information on desiccants in conjunction with a weighting scheme developed for this application, three desiccants were selected and tested in a bench-scale system at the Energy and Environmental Research Center (EERC). System performance at the bench scale aided in determining which desiccant was best suited for further evaluation. The results of the bench-scale tests along with further review of the available property data for each of the desiccants resulted in the selection of calcium chloride as the desiccant for testing at the pilot-scale level. Two weeks of testing utilizing natural gas in Test Series I and coal in Test Series II for production of flue gas was conducted with the liquid desiccant dehumidification system (LDDS) designed and built for this study. In general, it was found that the LDDS operated well and could be placed in an automode in which the process would operate with no operator intervention or adjustment. Water produced from this process should require little processing for use, depending on the end application. Test Series II water quality was not as good as that obtained in Test Series I; however, this was believed to be due to a system upset that contaminated the product water system during Test Series II. The amount of water that can be recovered from flue gas with the LDDS is a function of several variables, including desiccant temperature, L/G in the absorber, flash drum pressure, liquid-gas contact method, and desiccant concentration. Corrosion will be an issue with the use of calcium chloride as expected but can be largely mitigated through proper material selection. Integration of the LDDS with either low-grade waste heat and or ground-source heating and cooling can affect the parasitic power draw the LDDS will have on a power plant. Depending on the amount of water to be removed from the flue gas, the system can be designed with no parasitic power draw on the power plant other than pumping loads. This can be accomplished in one scenario by taking advantage of the heat of absorption and the heat of vaporization to provide the necessary temperature changes in the desiccant with the flue gas and precipitates that may form and how to handle them. These questions must be addressed in subsequent testing before scale-up of the process can be confidently completed.

Bruce C. Folkedahl; Greg F. Weber; Michael E. Collings

2006-06-30T23:59:59.000Z

163

NETL: IEP ? Post-Combustion CO2 Emissions Control - Flue Gas...  

NLE Websites -- All DOE Office Websites (Extended Search)

Flue Gas Purification Utilizing SOx NOx Reactions During Compression of CO2 Derived from Oxyfuel Combustion Project No.: DE-NT0005309 Air Products and Chemicals Inc. will...

164

Co-Removal of Mercury from Coal-Fired Power Plant Flue Gas with...  

NLE Websites -- All DOE Office Websites (Extended Search)

combustion conditions, and air pollution control devices upstream of a power plant FGD system have an impact on the types and concentration of flue gas mercury at the...

165

Microsoft Word - Flue Gas Moisture.Final Report.Abstract.Summary...  

NLE Websites -- All DOE Office Websites (Extended Search)

were performed to determine the relationship between flue gas moisture concentration, heat exchanger design and operating conditions, and water vapor condensation rate. The...

166

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

E-Print Network (OSTI)

efficiency by sulfur and/or chlorine containing compounds atfired Flue Gas by Sulfur-chlorine Compounds Nai-Qiang Yanremoval. Two sulfur-chlorine compounds, sulfur dichloride (

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

2008-01-01T23:59:59.000Z

167

Thermal oxidation vitrification flue gas elimination system  

SciTech Connect

With minor modifications to a Best Demonstrated Available Technology hazardous waste incinerator, it is possible to obtain combustion without potentially toxic emissions by using technology currently employed in similar applications throughout industry. Further, these same modifications will reduce waste handling over an extended operating envelope while minimizing energy consumption. Three by-products are produced: industrial grade carbon dioxide, nitrogen, and a final waste form that will exceed Toxicity Characteristics Leaching Procedures requirements and satisfy nuclear waste product consistency tests. The proposed system utilizes oxygen rather than air as an oxidant to reduce the quantities of total emissions, improve the efficiency of the oxidation reactions, and minimize the generation of toxic NO{sub x} emissions. Not only will less potentially hazardous constituents be generated; all toxic substances can be contained and the primary emission, carbon dioxide -- the leading ``greenhouse gas`` contributing to global warming -- will be converted to an industrial by-product needed to enhance the extraction of energy feedstocks from maturing wells. Clearly, the proposed configuration conforms to the provisions for Most Achievable Control Technology as defined and mandated for the private sector by the Clear Air Act Amendments of 1990 to be implemented in 1997 and still lacking definition.

Kephart, W. [Foster-Wheeler Environmental Corp., Oak Ridge, TN (United States); Angelo, F. [Resource Energy Corp. (United States); Clemens, M. [Argonne National Lab., IL (United States)

1995-06-01T23:59:59.000Z

168

Fundamentals of Mercury Oxidation in Flue Gas  

SciTech Connect

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 3 results for the experimental and modeling tasks. Experiments have been completed on the effects of chlorine. However, the experiments with sulfur dioxide and NO, in the presence of water, suggest that the wet-chemistry analysis system, namely the impingers, is possibly giving erroneous results. Future work will investigate this further and determine the role of reactions in the impingers on the oxidation results. The solid-phase experiments have not been completed and it is anticipated that only preliminary work will be accomplished during this study.

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

2006-07-31T23:59:59.000Z

169

Fundamentals of Mercury Oxidation in Flue Gas  

SciTech Connect

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

170

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

Science Conference Proceedings (OSTI)

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

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

2004-04-01T23:59:59.000Z

171

Fundamentals of Mercury Oxidation in Flue Gas  

SciTech Connect

The objective of this project was to understand the importance of and the contribution of gas-phase and solid-phase coal constituents in the mercury oxidation reactions. The project involved both experimental and modeling efforts. The team was comprised of the University of Utah, Reaction Engineering International, and the University of Connecticut. The objective was to determine the experimental parameters of importance in the homogeneous and heterogeneous oxidation reactions; validate models; and, improve existing models. Parameters studied include HCl, NO{sub x}, and SO{sub 2} concentrations, ash constituents, and temperature. The results suggested that homogeneous mercury oxidation is below 10% which is not consistent with previous data of others and work which was completed early in this research program. Previous data showed oxidation above 10% and up to 100%. However, the previous data are suspect due to apparent oxidation occurring within the sampling system where hypochlorite ion forms in the KCl impinger, which in turn oxidized mercury. Initial tests with entrained iron oxide particles injected into a flame reactor suggest that iron present on fly ash particle surfaces can promote heterogeneous oxidation of mercury in the presence of HCl under entrained flow conditions. Using the data generated above, with homogeneous reactions accounting for less than 10% of the oxidation, comparisons were made to pilot- and full-scale data. The results suggest that heterogeneous reactions, as with the case of iron oxide, and adsorption on solid carbon must be taking place in the full-scale system. Modeling of mercury oxidation using parameters from the literature was conducted to further study the contribution of homogeneous pathways to Hg oxidation in coal combustion systems. Calculations from the literature used rate parameters developed in different studies, in some cases using transition state theory with a range of approaches and basis sets, and in other cases using empirical approaches. To address this, rate constants for the entire 8-step homogeneous Hg oxidation sequence were developed using an internally consistent transition state approach. These rate constants when combined with the appropriate sub-mechanisms produced lower estimates of the overall extent of homogeneous oxidation, further suggesting that heterogeneous pathways play an important role in Hg oxidation in coal-fired systems.

JoAnn Lighty; Geoffrey Silcox; Constance Senior; Joseph Helble; Balaji Krishnakumar

2008-07-31T23:59:59.000Z

172

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

Science Conference Proceedings (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

173

Near-zero Emissions Oxy-combustion Flue Gas Purification  

NLE Websites -- All DOE Office Websites (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

174

Recovery of CO/sub 2/ from flue gas  

SciTech Connect

Within the Permian Basin geographic region, there are a variety of sources for CO/sub 2/ other than naturally occurring deposits. These sources can provide sufficient quantities of CO/sub 2/ for enhanced oil recovery (EOR) projects. The cost associated with pipelining CO/sub 2/ produced from natural sources into the Permian Basin is reported to be $1.50/MSCF or less. Therefore, flue gas sources result in higher CO/sub 2/ costs than natural deposits. However, these costs are within the pricing parameters for the normal CO/sub 2/ market place. The demand for flue gas CO/sub 2/ for EOR is seen to depend largely on the success of CO/sub 2/ floods and the relative price that can be applied to CO/sub 2/ based on the price of oil and the increases in domestic oil production and gas liquids that CO/sub 2/ can provide. Under current conditions, CO/sub 2/ has a value of ca $2.00/MSCF for EOR use.

Hyde, E.P.

1983-01-01T23:59:59.000Z

175

Supported polyethylenimine adsorbents for CO2 capture from flue gas  

Science Conference Proceedings (OSTI)

Anthropogenic CO2 emissions produced from fossil fuel combustion are believed to contribute to undesired consequences in global climate. Major contributors towards CO2 emissions are fossil fuel-fired power plants for electricity production. For this reason, CO2 capture from flue gas streams together with permanent sequestration in geologic formations is being considered a viable solution towards mitigation of the major greenhouse gas1. Technologies based on chemical absorption with alkanolamines have been assessed for first generation CO2 post-combustion capture primarily due to its advanced stage of development. However, limitations associated with these chemical solvents (i.e., low CO2 loadings, amine degradation by oxygen, equipment corrosion) manifest themselves in high capital and operating costs with reduced thermal efficiencies. Therefore, necessary design and development of alternative, lower cost approaches for CO2 capture from coal-fired combustion streams are warranted.

Fauth, D.J.; Gray, M.L.; Pennline, H.W.

2008-10-01T23:59:59.000Z

176

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

Science Conference Proceedings (OSTI)

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

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

2001-01-01T23:59:59.000Z

177

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

178

NETL: CO2 Capture from Flue Gas Using Solid Molecular Basket...  

NLE Websites -- All DOE Office Websites (Extended Search)

molecular basket sorbent for CO2 capture from flue gas. Energy Fuels 2011, 25, 456-458. XX Wang, SQ Zhao, XL Ma, CS Song, CO2 capture from gas streams with low CO2...

179

Biomimetric Membrane for CO2 Capture from Flue Gas  

NLE Websites -- All DOE Office Websites (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

180

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

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

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

2004-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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
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181

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

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

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

2001-05-01T23:59:59.000Z

182

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

Fossil fuels used for power generation, transportation, and by industry are the primary source of anthropogenic CO{sub 2} emissions to the atmosphere. Much of the CO{sub 2} emission reduction effort will focus on large point sources, with fossil fuel fired power plants being a prime target. The CO{sub 2} content of power plant flue gas varies from 4% to 9% (vol), depending on the type of fossil fuel used and on operating conditions. Although new power generation concepts that may result in CO{sub 2} control with minimal economic penalty are under development, these concepts are not generally applicable to the large number of existing power plants.

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

2002-07-01T23:59:59.000Z

183

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

Open Energy Info (EERE)

efficiency+ commercial building energy efficiency+ industrial energy efficiency+ power plant energy efficiency+ Home Increase Natural Gas Energy Efficiency Description:...

184

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

185

Biomimetic Membrane for CO2 Capture from Flue Gas  

SciTech Connect

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

186

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

SciTech Connect

This project Final Report is submitted to the U.S. Department of Energy (DOE) as part of Cooperative Agreement DE-FC26-03NT41987, 'Sorbent Injection for Small ESP Mercury Control in Low Sulfur Eastern Bituminous Coal Flue Gas.' Sorbent injection technology is targeted as the primary mercury control process on plants burning low/medium sulfur bituminous coals equipped with ESP and ESP/FGD systems. About 70% of the ESPs used in the utility industry have SCAs less than 300 ft2/1000 acfm. Prior to this test program, previous sorbent injection tests had focused on large-SCA ESPs. This DOE-NETL program was designed to generate data to evaluate the performance and economic feasibility of sorbent injection for mercury control at power plants that fire bituminous coal and are configured with small-sized electrostatic precipitators and/or an ESP-flue gas desulfurization (FGD) configuration. EPRI and Southern Company were co-funders for the test program. Southern Company and Reliant Energy provided host sites for testing and technical input to the project. URS Group was the prime contractor to NETL. ADA-ES and Apogee Scientific Inc. were sub-contractors to URS and was responsible for all aspects of the sorbent injection systems design, installation and operation at the different host sites. Full-scale sorbent injection for mercury control was evaluated at three sites: Georgia Power's Plant Yates Units 1 and 2 [Georgia Power is a subsidiary of the Southern Company] and Reliant Energy's Shawville Unit 3. Georgia Power's Plant Yates Unit 1 has an existing small-SCA cold-side ESP followed by a Chiyoda CT-121 wet scrubber. Yates Unit 2 is also equipped with a small-SCA ESP and a dual flue gas conditioning system. Unit 2 has no SO2 control system. Shawville Unit 3 is equipped with two small-SCA cold-side ESPs operated in series. All ESP systems tested in this program had SCAs less than 250 ft2/1000 acfm. Short-term parametric tests were conducted on Yates Units 1 and 2 to evaluate the performance of low-cost activated carbon sorbents for removing mercury. In addition, the effects of the dual flue gas conditioning system on mercury removal performance were evaluated as part of short-term parametric tests on Unit 2. Based on the parametric test results, a single sorbent (e.g., RWE Super HOK) was selected for a 30-day continuous injection test on Unit 1 to observe long-term performance of the sorbent as well as its effects on ESP and FGD system operations as well as combustion byproduct properties. A series of parametric tests were also performed on Shawville Unit 3 over a three-week period in which several activated carbon sorbents were injected into the flue gas duct just upstream of either of the two Unit 3 ESP units. Three different sorbents were evaluated in the parametric test program for the combined ESP 1/ESP 2 system in which sorbents were injected upstream of ESP 1: RWE Super HOK, Norit's DARCO Hg, and a 62:38 wt% hydrated lime/DARCO Hg premixed reagent. Five different sorbents were evaluated for the ESP 2 system in which activated carbons were injected upstream of ESP 2: RWE Super HOK and coarse-ground HOK, Norit's DARCO Hg and DARCO Hg-LH, and DARCO Hg with lime injection upstream of ESP 1. The hydrated lime tests were conducted to reduce SO3 levels in an attempt to enhance the mercury removal performance of the activated carbon sorbents. The Plant Yates and Shawville studies provided data required for assessing carbon performance and long-term operational impacts for flue gas mercury control across small-sized ESPs, as well as for estimating the costs of full-scale sorbent injection processes.

Carl Richardson; Katherine Dombrowski; Douglas Orr

2006-12-31T23:59:59.000Z

187

Pore structure and reactivity changes in hot coal gas desulfurization sorbents  

Science Conference Proceedings (OSTI)

The primary objective of the project was the investigation of the pore structure and reactivity changes occurring in metal/metal oxide sorbents used for desulfurization of hot coal gas during sulfidation and regeneration, with particular emphasis placed on the effects of these changes on the sorptive capacity and efficiency of the sorbents. Commercially available zinc oxide sorbents were used as model solids in our experimental investigation of the sulfidation and regeneration processes.

Sotirchos, S.V.

1991-05-01T23:59:59.000Z

188

Method and apparatus for enhancing the desulfurization of hot coal gas in a fluid-bed coal gasifier  

DOE Patents (OSTI)

A process and apparatus for providing additional desulfurization of the hot gas produced in a fluid-bed coal gasifier, within the gasifier is described. A fluid-bed of iron oxide is located inside the gasifier above the gasification bed in a fluid-bed coal gasifier in which in-bed desulfurization by lime/limestone takes place. The product gases leave the gasification bed typically at 1600 to 1800 F and are partially quenched with water to 1000 to 1200 F before entering the iron oxide bed. The iron oxide bed provides additional desulfurization beyond that provided by the lime /limestone. 1 fig.

Grindley, T.

1988-04-05T23:59:59.000Z

189

Integrated operation of a pressurized fixed bed gasifier and hot gas desulfurization system  

SciTech Connect

The primary objective of this contract continues to be the demonstration of high fuel gas desulfurization of high temperature fuel gas desulfurization and particulate removal using a moving bed process with regenerable metal oxide sorbent. The fuel gas source for test operation is a fixed bed, air blown gasifier located at GE Corporate Research and Development in Schenectady, New York. The demonstration project also includes the design, construction, installation and test operation of a gas turbine simulator which includes a modified GE MS6000 type gas turbine combustor and a film cooled, first stage LM 6000 nozzle assembly. The hot gas cleanup (HGCU) system and the gas turbine simulator have been designed to operate with the full 8000 lb/hr fuel gas flow from the gasification of 1800 lb/hr of coal at 280 psig and 1000 to 1150 F. An advanced formulation of zinc ferrite as well as zinc titanate have been used as the regenerable metal oxide sorbents in testing to date. Demonstration of halogen removal as well as characterization of alkali and heavy metal concentrations in the fuel gas remain objectives, as well. Results are discussed.

Cook, C.S.; Gal, E.; Furman, A.H.; Ayala, R.

1992-12-01T23:59:59.000Z

190

Integrated operation of a pressurized fixed bed gasifier and hot gas desulfurization system  

SciTech Connect

The primary objective of this contract continues to be the demonstration of high fuel gas desulfurization of high temperature fuel gas desulfurization and particulate removal using a moving bed process with regenerable metal oxide sorbent. The fuel gas source for test operation is a fixed bed, air blown gasifier located at GE Corporate Research and Development in Schenectady, New York. The demonstration project also includes the design, construction, installation and test operation of a gas turbine simulator which includes a modified GE MS6000 type gas turbine combustor and a film cooled, first stage LM 6000 nozzle assembly. The hot gas cleanup (HGCU) system and the gas turbine simulator have been designed to operate with the full 8000 lb/hr fuel gas flow from the gasification of 1800 lb/hr of coal at 280 psig and 1000 to 1150 F. An advanced formulation of zinc ferrite as well as zinc titanate have been used as the regenerable metal oxide sorbents in testing to date. Demonstration of halogen removal as well as characterization of alkali and heavy metal concentrations in the fuel gas remain objectives, as well. Results are discussed.

Cook, C.S.; Gal, E.; Furman, A.H.; Ayala, R.

1992-01-01T23:59:59.000Z

191

Analysis of Halogen-Mercury Reactions in Flue Gas  

SciTech Connect

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

192

Membrane Process to Sequester CO2 from Power Plant Flue Gas  

NLE Websites -- All DOE Office Websites (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

193

pH Adjustment of Power Plant Cooling Water with Flue Gas/Fly Ash  

to fossil fuel burning power plants to control mineral precipitation in cooling water. Flue gas, which is 10% CO2, could be diverted into a plant’s cooling water

194

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

195

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 gas streams to electricity. The NTU-effectiveness method, exergy, and ...

Latcham, Jacob G. (Jacob Greco)

2009-01-01T23:59:59.000Z

196

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

E-Print Network (OSTI)

from flue gas of coal-fired power plants. Environ. Sci. &Technologies for Coal-Fired Power Plants, DOE/NETL Mercurynumber of coal-fired generating plants (1-3). The mercury is

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

2008-01-01T23:59:59.000Z

197

CO2 Capture from Flue Gas Using SOlid Molecular Basket Sorbents  

NLE Websites -- All DOE Office Websites (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-

198

CO2 Removal from Flue Gas Using MIcroporous Metal Organic Frameworks  

NLE Websites -- All DOE Office Websites (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

199

Flue Gas Sulfuric Acid Measurement Method Improvements: Second Interim Report, December 2000  

Science Conference Proceedings (OSTI)

The objective of this project is to improve the ability of electric utilities with coal and oil-fired power plants to measure and report sulfuric emissions. Most coal and oil-fired utility boilers will trigger Toxic Release Inventory (TRI) reporting for sulfuric acid. The Controlled Condensation System (CCS) method for measuring flue gas sulfuric acid concentrations is believed to provide one of the best methods for measuring sulfuric acid in flue gas. However, there are situations where the CCS method m...

2000-12-05T23:59:59.000Z

200

Noble Metal Catalysts for Mercury Oxidation in Utility Flue Gas: Gold, Palladium and Platinum Formulations  

Science Conference Proceedings (OSTI)

The use of noble metals as catalysts for mercury oxidation in flue gas remains an area of active study. To date, field studies have focused on gold and palladium catalysts installed at pilot scale. In this article, we introduce bench-scale experimental results for gold, palladium and platinum catalysts tested in realistic simulated flue gas. Our initial results reveal some intriguing characteristics of catalytic mercury oxidation and provide insight for future research into this potentially important process.

Presto, A.A.; Granite, E.J

2008-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

Method for removing heavy metal and nitrogen oxides from flue gas, device for removing heavy metal and nitrogen oxides from flue gas  

DOE Patents (OSTI)

A method for the simultaneous removal of oxides and heavy metals from a fluid is provided comprising combining the fluid with compounds containing alkali and sulfur to create a mixture; spray drying the mixture to create a vapor phase and a solid phase; and isolating the vapor phase from the solid phase. A device is also provided comprising a means for spray-drying flue gas with alkali-sulfide containing liquor at a temperature sufficient to cause the flue gas to react with the compounds so as to create a gaseous fraction and a solid fraction and a means for directing the gaseous fraction to a fabric filter.

Huang, Hann-Sheng; Livengood, Charles David

1997-12-01T23:59:59.000Z

202

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

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

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

2003-08-01T23:59:59.000Z

203

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

Science Conference Proceedings (OSTI)

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

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

2003-01-01T23:59:59.000Z

204

Status of METC investigations of coal gas desulfurization at high temperature. [Zinc ferrite  

DOE Green Energy (OSTI)

This report documents the continuing effort at the US Department of Energy/Morgantown Energy Technology Center (METC) to develop a hot-gas desulfurization process for coal-derived gas, primarily for application to molten carbonate fuel cells. Metal oxide sorbents were tested on lab-scale test equipment, and it was determined that scale-up of the process was warranted. A larger, skid-mounted test unit was therefore designed, constructed, and installed on a sidestream of the DOE/METC fixed-bed gasifier. A first series of tests was conducted during Gasifier Run 101. These tests served to shake down the test unit, and provide data on the performance of the test unit operating on coal-derived gas. Overall, the process operated well on fixed-bed, air-blown gasifier gas. Sulfur levels in exit dry gas were reduced to less than 10 ppM. Regeneration appears to restore the sulfur-removing capacity of the sorbent. Sorbent integrity was maintained during the test period, which incorporated three sulfidations. It is recommended that treatment of the regeneration offgas be investigated, and that testing and development of a system to reduce the sulfur in this gas to elemental sulfur be initiated. In addition, it is suggested that a multiple reactor system be planned for continuous operation, to allow for long-term tests of downstream users of desulfurized gas. 7 references, 18 figures, 9 tables.

Steinfeld, G.

1984-03-01T23:59:59.000Z

205

Use of sulfide-containing liquors for removing mercury from flue gases  

DOE Patents (OSTI)

A method and apparatus for reducing and removing mercury in industrial gases, such as a flue gas, produced by the combustion of fossil fuels, such as coal, adds sulfide ions to the flue gas as it passes through a scrubber. Ideally, the source of these sulfide ions may include at least one of: sulfidic waste water, kraft caustic liquor, kraft carbonate liquor, potassium sulfide, sodium sulfide, and thioacetamide. The sulfide ion source is introduced into the scrubbing liquor as an aqueous sulfide species. The scrubber may be either a wet or dry scrubber for flue gas desulfurization systems.

Nolan, Paul S. (North Canton, OH); Downs, William (Alliance, OH); Bailey, Ralph T. (Uniontown, OH); Vecci, Stanley J. (Alliance, OH)

2003-01-01T23:59:59.000Z

206

Mathematical modeling of wet magnesia flue gas desulphurization process  

Science Conference Proceedings (OSTI)

Desulphurization of flue gases from various chemical industries in a techno-econo-enviro manner is a demanding technology. The concentrations of sulphur dioxide in and around these plants overshoot the danger point. In recent years, the process analysis ...

M. K. Mondal

2008-01-01T23:59:59.000Z

207

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

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

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

2002-04-01T23:59:59.000Z

208

Utilizing secondary heat to heat wash oil in the coke-oven gas desulfurization division  

SciTech Connect

Removal of hydrogen sulfide from the coke-oven gas by the vacuum-carbonate method involves significant energy costs, comprising about 47% of the total costs of the process. This is explained by the significant demand of steam for regeneration of the wash oil, the cost of which exceeds 30% of the total operating costs. The boiling point of the saturated wash oil under vacuum does not exceed 70/sup 0/C, thus the wash oil entering the regenerator can be heated either by the direct coke-oven gas or by the tar supernatant from the gas collection cycle. Utilizing the secondary heat of the direct coke-oven gas and the tar supernatant liquor (the thermal effect is approximately the same) to heat the wash oil from the gas desulfurization shops significantly improves the industrial economic indices. Heating the wash oil from gas desulfurization shops using the vacuum-carbonate method by the heat of the tar supernatant liquor may be adopted at a number of coking plants which have a scarcity of thermal resources and which have primary coolers with vertical tubes.

Volkov, E.L.

1981-01-01T23:59:59.000Z

209

Bench-Scale Demonstration of Hot-Gas Desulfurization Technology  

SciTech Connect

The U.S. Department of Energy (DOE), Federal Energy Technology Center (FETC), is sponsoring research in advanced methods for controlling contaminants in hot coal gasifier gas (coal-derived fuel-gas) streams of integrated gasification combined-cycle (IGCC) power systems. The hot gas cleanup work seeks to eliminate the need for expensive heat recovery equipment, reduce efficiency losses due to quenching, and minimize wastewater treatment costs.

Jeffrey W. Portzer; Santosh K. Gangwal

1998-12-01T23:59:59.000Z

210

Development of a hot-gas desulfurization system for IGCC applications  

SciTech Connect

Integrated gasification combined cycle (IGCC) power plants are being advanced worldwide to produce electricity from coal because of their superior environmental performance, economics, and efficiency in comparison to conventional coal-based power plants. One key component of an advanced IGCC power plant is a hot-gas desulfurization system employing regenerable sorbents. To carry out hot-gas desulfurization in a fluidized-bed reactor, it is necessary that the sorbents have high attrition resistance, while still maintaining high chemical reactivity and sulfur absorption capacity. Also, efficient processes are needed for the treatment of SO{sub 2}-containing regeneration off-gas to produce environmentally benign waste or useful byproducts. A series of durable zinc titanate sorbents were formulated and tested in a bench-scale fluidized-bed reactor system. Reactive sorbents were developed with addition resistance comparable to fluid-bed cracking (FCC) catalysts used in petroleum refineries. In addition, progress continues on the development of the Direct Sulfur Recovery Process (DSRP) for converting SO{sub 2} in the regeneration off-gas to elemental sulfur. Plans are under way to test these bench-scale systems at gasifier sites with coal gas. This paper describes the status and future plans for the demonstration of these technologies.

Gupta, R.; McMichael, W.J.; Gangwal, S.K. [Research Triangle Inst., Research Triangle Park, NC (United States); Jain, S.C.; Dorchak, T.P. [USDOE Morgantown Energy Technology Center, WV (United States)

1992-12-31T23:59:59.000Z

211

Near-Zero Emissions Oxy-Combustion Flue Gas Purification  

Science Conference Proceedings (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

212

Durable zinc oxide-containing sorbents for coal gas desulfurization  

DOE Patents (OSTI)

Durable zinc-oxide containing sorbent pellets for removing hydrogen sulfide from a gas stream at an elevated temperature are made up to contain titania as a diluent, high-surface-area silica gel as a matrix material, and a binder. These materials are mixed, moistened, and formed into pellets, which are then dried and calcined. The resulting pellets undergo repeated cycles of sulfidation and regeneration without loss of reactivity and without mechanical degradation. Regeneration of the pellets is carried out by contacting the bed with an oxidizing gas mixture.

Siriwardane, R.V.

1994-12-31T23:59:59.000Z

213

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

The objective of this project is to develop a simple, inexpensive process to separate CO{sub 2} as an essentially pure stream from a fossil fuel combustion system using a regenerable, sodium-based sorbent. The sorbent being used in this project is sodium carbonate which is converted to sodium bicarbonate, or ''baking soda,'' through reaction with carbon dioxide and water vapor. Sodium bicarbonate is regenerated to sodium carbonate when heated, producing a nearly pure CO{sub 2} stream after condensation of water vapor. This quarter, five cycle thermogravimetric tests were conducted at the Louisiana State University (LSU) with sodium bicarbonate Grade 3 (SBC{number_sign}3) which showed that carbonation activity declined slightly over 5 cycles following severe calcination conditions of 200 C in pure CO{sub 2}. Three different sets of calcination conditions were tested. Initial carbonation activity (as measured by extent of reaction in the first 25 minutes) was greatest subsequent to calcination at 120 C in He, slightly less subsequent to calcination in 80% CO{sub 2}/20% H{sub 2}O, and lowest subsequent to calcination in pure CO{sub 2} at 200 C. Differences in the extent of reaction after 150 minutes of carbonation, subsequent to calcination under the same conditions followed the same trend but were less significant. The differences between fractional carbonation under the three calcination conditions declined with increasing cycles. A preliminary fixed bed reactor test was also conducted at LSU. Following calcination, the sorbent removed approximately 19% of the CO{sub 2} in the simulated flue gas. CO{sub 2} evolved during subsequent calcination was consistent with an extent of carbonation of approximately 49%. Following successful testing of SBC{number_sign}3 sorbent at RTI reported in the last quarter, a two cycle fluidized bed reactor test was conducted with trona as the sorbent precursor, which was calcined to sodium carbonate. In the first carbonation cycle, CO{sub 2} removal rates declined from 20% to about 8% over the course of three hours. Following calcination, a second carbonation cycle was conducted, at a lower temperature with a lower water vapor content. CO{sub 2} removal and sorbent capacity utilization declined under these conditions. Modifications were made to the reactor to permit addition of extra water for testing in the next quarter. Thermodynamic analysis of the carbonation reaction suggested the importance of other phases, intermediate between sodium carbonate and sodium bicarbonate, and the potential for misapplication of thermodynamic data from the literature. An analysis of initial rate data from TGA experiments suggested that the data may fit a model controlled by the heat transfer from the sorbent particle surface to the bulk gas.

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

2002-01-01T23:59:59.000Z

214

Critical review of mercury chemistry in flue gas.  

SciTech Connect

Mercury (Hg) and its compounds have long been recognized as potentially hazardous to human health and the environment. Many man-made sources of mercury have been reduced in recent years through process changes and control measures. However, emissions of mercury from coal-fired power plants, while exceedingly dilute by the usual pollution standards, still constitute a major source when considered in the aggregate. Concerns over those emissions and the prospect of impending emissions regulations have led to a wide range of research projects dealing with the measurement and control of mercury in flue gas. This work has made considerable progress in improving the understanding of mercury emissions and their behavior, but inconsistencies and unexpected results have also shown that a better understanding of mercury chemistry is needed. To develop a more complete understanding of where additional research on mercury chemistry is needed, the U.S. Department of Energy (DOE) asked Argonne National Laboratory (Argonne) to conduct a critical review of the available information as reported in the technical literature. The objectives were to summarize the current state of the art of chemistry knowledge, identify significant knowledge gaps, and recommend future research to resolve those gaps. An initial evaluation of potential review topics indicated that the scope of the review would need to be limited and focused on the most important topics relative to mercury control. To aid in this process, Argonne developed a brief survey that was circulated to researchers in the field who could help identify and prioritize the many aspects of the problem. The results of the survey were then used to design and guide a highly focused literature search that identified key papers for analysis. Each paper was reviewed, summarized, and evaluated for the relevance and quality of the information presented. The results of that work provided the basis for conclusions regarding the state of knowledge of mercury chemistry and recommendations for further research. This report begins by summarizing the survey process and describing how the results were used to shape the critical review. Analyses of information obtained from the various publications are presented chronologically, beginning with the earliest relevant publication found and concluding with the end of the review in early 2003. Finally, the conclusions and recommendations for future research are presented. The survey instrument is included in Appendix A, while detailed information on each of the publications reviewed is given in Appendix B.

Mendelsohn, M. H.; Livengood, C. D.

2006-11-27T23:59:59.000Z

215

Desulfurization mixture and process for desulfurizing pig iron  

SciTech Connect

Process and composition for desulfurizing pig iron in which the desulfurization agent consists essentially of calcium carbide, a gas-evolving component and fluorspar; the advantage of the process and composition is that it reduces dust pollution and danger of flaming in the handling of the slag after the desulfurization of pig iron.

Freissmuth, A.; Gmohling, W.; Rock, H.

1982-02-16T23:59:59.000Z

216

The Influence of Flue Gas Recirculation on the Formation of NOx in the Process of Coal Grate-Fired  

Science Conference Proceedings (OSTI)

With the improvement of environmental protection requirements, the problems of NOx emission from industrial boiler become more and more notable. To explore a real effective method of low NOx combustion, the article discusses the influence of flue gas ... Keywords: flue gas recirculation, grate-fired, temperature, Nox

Li Xu; Jianmin Gao; Guangbo Zhao; Laifu Zhao; Zhifeng Zhao; Shaohua Wu

2011-03-01T23:59:59.000Z

217

The Discussion of a New Exhausting Smoke Solution in Natural Draft Cooling Tower with Flue Gas Injection  

Science Conference Proceedings (OSTI)

First, the three-dimensional model of NDCT with flue gas injection and the boundary conditions was established by GAMBIT2.3 on the basis of structural parameter. On theFLUENT6.3 technology platform with self-designed program, it was found that: The new ... Keywords: NDCT with flue gas injection, jet mechanics numerical simulation, natural draft cooling towers

Yang Shuo; Qing-Jie Qi; Xin-Le Yang; Shi Lei; Chun-Yang Li

2011-02-01T23:59:59.000Z

218

Air Toxics Control by Wet Flue Gas Desulfurization Systems: 2013 Update  

Science Conference Proceedings (OSTI)

With proposed changes in current emissions regulations and recent EPA initiatives, most power producers have concluded that tighter limits on mercury, NOx, SO2, and primary particulates are inevitable. Likewise, more stringent controls for power plant emissions emphasize the need for more cost-effective pollutant reduction approaches. This report provides an update on results from an ongoing EPRI project directed at enhancing “co-benefit” capture of mercury and ...

2013-12-05T23:59:59.000Z

219

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

220

A Manual on the Use of Flue Gas Conditioning for ESP Performance Enhancement  

Science Conference Proceedings (OSTI)

Flue gas conditioning can boost the effectiveness of electrostatic precipitators. This manual quantifies both the performance and the cost-benefits, with low-sulfur coals for example cases. It also outlines a procedure that will allow utilities to make estimates for their own units.

1985-08-02T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

"LIMITS AND CHANCES IN FLUE-GAS CLEANING -INTE RNATIONAL PERSPECTIVE"  

E-Print Network (OSTI)

) and elemental mercury (Hg«» under oxidizing conditions of the off-gases downstream of the refuse incinerator), sulfur dioxide (S02)' nitrogen oxides (NOx), carbon monoxide (CO), PCDDs/PCDFs, cadmium (Cd), mercury (Hg emission regulations. Mercury Control in MWCs The capture of Hg in flue gas cleaning devices depends on the

Columbia University

222

Method for reducing sulfate formation during regeneration of hot-gas desulfurization sorbents  

DOE Patents (OSTI)

The regeneration of sulfur sorbents having sulfate forming tendencies and used for desulfurizing hot product gas streams such as provided by coal gasification is provided by employing a two-stage regeneration method. Air containing a sub-stoichiometric quantity of oxygen is used in the first stage for substantially fully regenerating the sorbent without sulfate formation and then regeneration of the resulting partially regenerated sorbent is completed in the second stage with air containing a quantity of oxygen slightly greater than the stoichiometric amount adequate to essentially fully regenerate the sorbent. Sulfate formation occurs in only the second stage with the extent of sulfate formation being limited only to the portion of the sulfur species contained by the sorbent after substantially all of the sulfur species have been removed therefrom in the first stage.

Bissett, Larry A. (Morgantown, WV); Strickland, Larry D. (Morgantown, WV); Rockey, John M. (Westover, WV)

1994-01-01T23:59:59.000Z

223

Desulfurization of Fisher-Tropsch synthesis gas in coal-to-gasoline pilot plant  

SciTech Connect

In 1989, a coal-to-gasoline pilot plant was installed and operated successfully in China, and a dry desulfurization process was used in this plant. This paper presents an overview of the dry desulfurization process. It includes design and operation of the process, and a description of ST801, T305 adsorbents and TGH COS hydrolysis catalyst. In addition, the desulfurization process used in a planned demonstration plant scheduled for completion in 1991 is presented.

Shishao, T.; Ju, S.; Shenzhao, L.; Maoqian, M.; Hanxian, G. (Dept. of Chemical Engineering, Taiyuan Univ. of Technology, Taiyuan, Shanxi (CN))

1990-01-01T23:59:59.000Z

224

Solvent Formulation for CO2 Separation from Flue Gas Streams  

NLE Websites -- All DOE Office Websites (Extended Search)

gas characteristics (composition, pressure, temperature, etc.) and the treated gas specifications (i.e. the process requirements). These two elements provide a preliminary...

225

Optimal absorption pressure for CO/sub 2/ recovery from flue gas calculated  

SciTech Connect

This paper calculates the cost of separating carbon dioxide from flue gas for enhanced oil recovery (EOR). It diagrams a carbon dioxide recovery plant and presents tables with costs of carbon dioxide recovery at various absorption pressures, and cost in various EOR project. It shows that the utility cost is a dominant factor and that a gas compressor does not reduce the equipment cost effectively at low pressure and concludes that 70 psig is the optimal operating pressure.

Fang, C.S.; Fan, S.K.

1982-11-22T23:59:59.000Z

226

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

NLE Websites -- All DOE Office Websites (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

227

MEMBRANE PROCESS TO SEQUESTER CO2 FROM POWER PLANT FLUE GAS  

Science Conference Proceedings (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

228

SOLOX coke-oven gas desulfurization ppm levels -- No toxic waste  

SciTech Connect

For sulfur removal from coke-oven gas, the reduction/oxidation processes such as Stretford are the most effective, capable of removing the H[sub 2]S down to ppm levels. However, these processes have, in the past, suffered from ecological problems with secondary pollutant formation resulting from side reactions with HCN and O[sub 2]. The SOLOX gas desulfurization system is a development of the Stretford process in which the toxic effluent problems are eliminated by installing a salt decomposition process operating according to the liquid-phase hydrolysis principle. In this process, the gaseous hydrolysis products H[sub 2]S, NH[sub 3] and CO[sub 2] are returned to the untreated gas, and the regenerated solution is recycled to the absorption process. The blowdown from the absorption circuit is fed into a tube reactor where the hydrolysis process takes place. The toxic salts react with water, producing as reaction products the gases H[sub 2]S, NH[sub 3] and CO[sub 2], and the nontoxic salt Na[sub 2]SO[sub 4]. From the hydrolysis reactor the liquid stream flows into a fractionating crystallization plant. This plant produces a recycle stream of regenerated absorption solution and a second stream containing most of the Na[sub 2]SO[sub 4]. This second stream comprises the net plant waste and can be disposed of with the excess ammonia liquor or sprayed onto the coal.

Platts, M. (Thyssen Still Otto Technical Services, Pittsburgh, PA (United States)); Tippmer, K. (Thyssen Still Otto Anlagentechnik GmbH, Bochum (Germany))

1994-09-01T23:59:59.000Z

229

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 sequestration. In this thesis, I report my findings on the effect of flue gas ??impurities?? on the displacement of natural gas during CO2 sequestration, and results on unconfined compressive strength (UCS) tests to carbonate samples. In displacement experiments, corefloods were conducted at 1,500 psig and 70??C, in which flue gas was injected into an Austin chalk core containing initially methane. Two types of flue gases were injected: dehydrated flue gas with 13.574 mole% CO2 (Gas A), and treated flue gas (N2, O2 and water removed) with 99.433 mole% CO2 (Gas B). The main results of this study are as follows. First, the dispersion coefficient increases with concentration of ??impurities??. Gas A exhibits the largest dispersion coefficients, 0.18-0.25 cm2/min, compared to 0.13-0.15 cm2/min for Gas B, and 0.15 cm2/min for pure CO2. Second, recovery of methane at breakthrough is relatively high, ranging from 86% OGIP for pure CO2, 74-90% OGIP for Gas B, and 79-81% for Gas A. Lastly, injection of Gas A would sequester the least amount of CO2 as it contains about 80 mole% nitrogen. From the view point of sequestration, Gas A would be least desirable while Gas B appears to be the most desirable as separation cost would probably be cheaper than that for pure CO2 with similar gas recovery. For UCS tests, corefloods were conducted at 1,700 psig and 65??C in such a way that the cell throughput of CO2 simulates near-wellbore throughput. This was achieved through increasing the injection rate and time of injection. Corefloods were followed by porosity measurement and UCS tests. Main results are presented as follows. First, the UCS of the rock was reduced by approximately 30% of its original value as a result of the dissolution process. Second, porosity profiles of rock samples increased up to 2.5% after corefloods. UCS test results indicate that CO2 injection will cause weakening of near-wellbore formation rock.

Nogueira de Mago, Marjorie Carolina

2005-08-01T23:59:59.000Z

230

A pilot-scale Process Development Unit for transport and fluid-bed hot-gas desulfurization  

SciTech Connect

The Morgantown Energy Technology Center (METC) has designed and is currently constructing an on-site, hot gas desulfurization (HGD) Process Development Unit (PDU). The PDU is designed to use regenerable solid metal oxide sorbents that absorb hydrogen sulfide from high-temperature, high-pressure simulated coal-gasification fuel gas that is generated by a METC designed syngas generator. The simulated coal gas is a mixture of partially combusted natural gas, water, carbon dioxide, and hydrogen sulfide. PDU process conditions will be representative of anticipated commercial applications in terms of temperatures, pressures, compositions, velocities, and sorbent cycling. The PDU supports the Integrated Gasification Combined Cycle (IGCC) mission at METC by providing a test bed for development of IGCC cleanup systems that offer low capital cost, operating costs, and costs of electricity. METC intends to develop additional industrial involvement opportunities as the project progresses towards operations. The primary objectives of the PDU are to (1) fill the gap between small-scale testing and large-scale demonstration projects by providing a cost effective test site for transport and fluid-bed desulfurization reactor and sorbent development, (2) demonstrate sorbent suitability over a wide range of parameters, and (3) generate significant information on process control for transport and fluidized bed based desulfurization. PDU data is expected to be used to optimize process performance by expanding the experience for larger scale demonstration projects such as Sierra Pacific Power Company`s Clean Coal Technology project.

McMillian, M.H.; Bissett, L.A.

1996-09-01T23:59:59.000Z

231

Recovery of Water from Boiler Flue Gas Using Condensing Heat Exchangers  

Science Conference Proceedings (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

232

Recovery of Water from Boiler Flue Gas Using Condensing Heat Exchangers  

Science Conference Proceedings (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

233

Advanced gasifier-desulfurizer process development for SNG (substitute natural gas) application. Final report, August 1987-December 1988  

Science Conference Proceedings (OSTI)

KRW conducted investigations of calcium-promoted coal pyrolysis and gasification by means of bench-scale studies and an oxygen-blown PDU test. Results were used in a design study of a commercial KRW gasifier-desulfurizer, operating on Pittsburgh No. 8 coal and limestone for production of SNG. Bench-scale fluid-bed reactor studies were conducted with various fluidizing gases at temperatures and pressures of 1650 to 1950 F and 40 to 450 psig, with and without limestone, to give methane-yield and tar-yield data. The gasification kinetics studies of chars produced gave data which showed that limestone increases char reactivity and exerts a catalytic effect. Methane yields correlated exponentially to pressure. The bench-scale test results lead to an expectation that feeding some of the coal to the upper portion of the gasifier will increase methane yield and decrease oxygen consumption. In two PDU test-set points, expected operability and performance of the oxygen-blown gasifier-desulfurizer were confirmed. In Set Point 2, in-bed desulfurization efficiency was 88% and the product-gas higher heating value was 302 Btu/scf. The test results provided inputs to the design study of a KRW gasifier-desulfurizer island for production of 125 MM Btu/day of SNG. Results included a 4 to 6% improvement in feedstock inputs when compared to an earlier GRI-sponsored study. Methane yield decreased but the number of operating gasifier-desulfurizers remained at five. Equipment costs are expected to remain well within the previous + or - 25% cost estimate.

Blinn, M.B.; Cover, A.E.; Haldipur, G.B.; Datta, S.C.; Holmgren, J.D.

1989-06-01T23:59:59.000Z

234

Pore structure and reactivity changes in hot coal gas desulfurization sorbents. Final report, September 1987--January 1991  

SciTech Connect

The primary objective of the project was the investigation of the pore structure and reactivity changes occurring in metal/metal oxide sorbents used for desulfurization of hot coal gas during sulfidation and regeneration, with particular emphasis placed on the effects of these changes on the sorptive capacity and efficiency of the sorbents. Commercially available zinc oxide sorbents were used as model solids in our experimental investigation of the sulfidation and regeneration processes.

Sotirchos, S.V.

1991-05-01T23:59:59.000Z

235

Explaining the differential solubility of flue gas components in ionic liquids from first-principle calculations  

SciTech Connect

Flue gas is greatly responsible for acid rain formation and global warming. New generation ionic liquids (ILs) have potential in controlling the flue gas emissions, as they acquire high absorptivity for the component gases SO{sub 2}, CO{sub 2}, etc. The association of the IL-gas interactions to the absorptivity of gas molecules in ILs is, however, poorly understood. In this paper, we present a molecular level description of the interactions of ILs with SO{sub 2}, CO{sub 2}, and N{sub 2} and show its implications to the differential gas solubility. Our results indicate that the IL anion-gas interactions play a key role in deciding the gas solubility in ILs, particularly for polar gases such as SO{sub 2}. On the other hand, regular solution assumption applies to -2 solubility. In accordance with the previous theoretical and experimental findings, our results also imply that the IL anions dominate the interactions with gas molecules while the cations play a secondary role and the underlying fluid structures of the ILs remain unperturbed by the addition of gas molecules.

Prasad, B.R.; Senapati, S. [Indian Institute of Technology, Madras (India). Dept. of Biotechnology

2009-04-15T23:59:59.000Z

236

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

NLE Websites -- All DOE Office Websites (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

237

Environmental performance of air staged combustor with flue gas recirculation to burn coal/biomass  

DOE Green Energy (OSTI)

The environmental and thermal performance of a 1.07 m diameter, 440 kW atmospheric fluidized bed combustor operated at 700{degrees}C-920{degrees}C and burning coal was studied. Flue gas recirculation was incorporated to enhance the thermal performance and air staging was used to control emissions of SO{sub 2}, CO, NO{sub x} and N{sub 2}O. Studies focused on the effect of excess air, firing rate, and use of sorbent on system performance. The recirculation-staging mode with limestone had the highest thermal efficiency (0.67) using the firing equation. Emission data showed that flue gas recirculation (ratio of 0.7) significantly reduced NO{sub x} emissions; and that use of limestone sorbent at a Ca/S ratio of 3 reduced SO{sub 2} emissions by 64% to approximately 0.310 g/MJ.

Anuar, S.H.; Keener, H.M.

1995-12-31T23:59:59.000Z

238

Microalgae Production from Power Plant Flue Gas: Environmental Implications on a Life Cycle Basis  

DOE Green Energy (OSTI)

Power-plant flue gas can serve as a source of CO{sub 2} for microalgae cultivation, and the algae can be cofired with coal. This life cycle assessment (LCA) compared the environmental impacts of electricity production via coal firing versus coal/algae cofiring. The LCA results demonstrated lower net values for the algae cofiring scenario for the following using the direct injection process (in which the flue gas is directly transported to the algae ponds): SOx, NOx, particulates, carbon dioxide, methane, and fossil energy consumption. Carbon monoxide, hydrocarbons emissions were statistically unchanged. Lower values for the algae cofiring scenario, when compared to the burning scenario, were observed for greenhouse potential and air acidification potential. However, impact assessment for depletion of natural resources and eutrophication potential showed much higher values. This LCA gives us an overall picture of impacts across different environmental boundaries, and hence, can help in the decision-making process for implementation of the algae scenario.

Kadam, K. L.

2001-06-22T23:59:59.000Z

239

Flue gas conditioning for improved particle collection in electrostatic precipitators. Quarterly technical report  

SciTech Connect

The purpose of this research program is to identify and evaluate a variety of additives capable of increasing particle cohesion which could be used for improving collection efficiency in an ESP. A three-phase screening process will be used to provide the, evaluation of many additives in a logical and cost-effective manner. The three step approach involves the following experimental setups: 1. Provide a preliminary screening in the laboratory by measuring the effects of various conditioning agents on reentrainment of flyash particles in an electric field operating at simulated flue gas conditions. 2. Evaluate the successful additives using a 100 acfm bench-scale ESP operating on actual flue gas. 3. Obtain the data required for scaling up the technology by testing the two or three most promising conditioning agents at the pilot scale.

Durham, M.D.

1992-04-27T23:59:59.000Z

240

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

NLE Websites -- All DOE Office Websites (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

Note: This page contains sample records for the topic "flue gas desulfurization" 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.


241

Membrane Process to Capture CO2 from Power Plant Flue Gas  

NLE Websites -- All DOE Office Websites (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

242

Effects of Chlorine and Other Flue Gas Parameters on SCR Catalyst Mercury Oxidation and Capture Efficiencies  

Science Conference Proceedings (OSTI)

Although catalyst behavior is relatively well understood with respect to deNOx and SO2 oxidation, relatively little is known about mercury oxidation behavior. This test program seeks to evaluate the mercury oxidation performance of multiple types of Selective Catalytic Reduction (SCR) catalyst as a function of changes in various flue gas parameters, including chlorine level, ammonia level, flow rate, and temperature. This interim report describes the results from parametric testing on the first catalyst.

2008-08-27T23:59:59.000Z

243

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

Science Conference Proceedings (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

244

Fundamental mechanisms in flue gas conditioning. Quarterly report, January 1994--March 1994  

Science Conference Proceedings (OSTI)

We are currently performing a series of pilot-scale tests designed to determine the effects that adsorbed water has on fabric filtration and electrostatic precipitation of entrained fly ash particles in actual flue gas environments. We are investigating two key phenomena in our pilot-scale tests. The first is the ability of flue gas humidification to increase ash cohesivity through the creation of liquid bridges between particles collected in a fabric filter. Increasing cohesivity through the development of liquid bridges was demonstrated in our laboratory measurements of tensile strength and uncompacted bulk porosity, and in filtration studies performed for DOE/PETC under an earlier contract. With the range of coals that will be fired in Southern Research Institute`s Coal Combustion Facility (CCF), filtration tests should verify how different fly ashes react to water conditioning in actual flue gas environments. The CCF provides a valuable test location for our studies. The second phenomenon we plan to study is the electrostatic reentrainment of previously collected ash particles in an ESP. We have prepared a small ESP for use in our pilot-scale tests. Our laboratory studies have shown the effects that relative humidity can have on the forces that hold the collected ash on the grounded ESP plate.

Snyder, T.R.

1994-04-18T23:59:59.000Z

245

SNOX Flue Gas Cleaning Demonstration Project: A DOE Assessment  

NLE Websites -- All DOE Office Websites (Extended Search)

SO 2 to SO 3 . The exit gas from the SO 3 converter passes through a novel glass-tube condenser in which the SO 3 is hydrated to H 2 SO 4 vapor and then condensed to a concentrated...

246

Catalysts for oxidation of mercury in flue gas  

DOE Patents (OSTI)

Two new classes of catalysts for the removal of heavy metal contaminants, especially mercury (Hg) from effluent gases. Both of these classes of catalysts are excellent absorbers of HCl and Cl.sub.2 present in effluent gases. This adsorption of oxidizing agents aids in the oxidation of heavy metal contaminants. The catalysts remove mercury by oxidizing the Hg into mercury (II) moieties. For one class of catalysts, the active component is selected from the group consisting of iridium (Ir) and iridum-platinum (Ir/Pt) alloys. The Ir and Ir/Pt alloy catalysts are especially corrosion resistant. For the other class of catalyst, the active component is partially combusted coal or "Thief" carbon impregnated with Cl.sub.2. Untreated Thief carbon catalyst can be self-activating in the presence of effluent gas streams. The Thief carbon catalyst is disposable by means of capture from the effluent gas stream in a particulate collection device (PCD).

Granite, Evan J. (Wexford, PA); Pennline, Henry W. (Bethel Park, PA)

2010-08-17T23:59:59.000Z

247

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

SciTech Connect

This final report describes work conducted for the U.S. Department of Energy National Energy Technology Laboratory (DOE NETL) on development of an efficient membrane process to capture carbon dioxide (CO{sub 2}) from power plant flue gas (award number DE-NT0005312). The primary goal of this research program was to demonstrate, in a field test, the ability of a membrane process to capture up to 90% of CO{sub 2} in coal-fired flue gas, and to evaluate the potential of a full-scale version of the process to perform this separation with less than a 35% increase in the levelized cost of electricity (LCOE). Membrane Technology and Research (MTR) conducted this project in collaboration with Arizona Public Services (APS), who hosted a membrane field test at their Cholla coal-fired power plant, and the Electric Power Research Institute (EPRI) and WorleyParsons (WP), who performed a comparative cost analysis of the proposed membrane CO{sub 2} capture process. The work conducted for this project included membrane and module development, slipstream testing of commercial-sized modules with natural gas and coal-fired flue gas, process design optimization, and a detailed systems and cost analysis of a membrane retrofit to a commercial power plant. The Polaris™ membrane developed over a number of years by MTR represents a step-change improvement in CO{sub 2} permeance compared to previous commercial CO{sub 2}-selective membranes. During this project, membrane optimization work resulted in a further doubling of the CO{sub 2} permeance of Polaris membrane while maintaining the CO{sub 2}/N{sub 2} selectivity. This is an important accomplishment because increased CO{sub 2} permeance directly impacts the membrane skid cost and footprint: a doubling of CO{sub 2} permeance halves the skid cost and footprint. In addition to providing high CO{sub 2} permeance, flue gas CO{sub 2} capture membranes must be stable in the presence of contaminants including SO{sub 2}. Laboratory tests showed no degradation in Polaris membrane performance during two months of continuous operation in a simulated flue gas environment containing up to 1,000 ppm SO{sub 2}. A successful slipstream field test at the APS Cholla power plant was conducted with commercialsize Polaris modules during this project. This field test is the first demonstration of stable performance by commercial-sized membrane modules treating actual coal-fired power plant flue gas. Process design studies show that selective recycle of CO{sub 2} using a countercurrent membrane module with air as a sweep stream can double the concentration of CO{sub 2} in coal flue gas with little energy input. This pre-concentration of CO{sub 2} by the sweep membrane reduces the minimum energy of CO{sub 2} separation in the capture unit by up to 40% for coal flue gas. Variations of this design may be even more promising for CO{sub 2} capture from NGCC flue gas, in which the CO{sub 2} concentration can be increased from 4% to 20% by selective sweep recycle. EPRI and WP conducted a systems and cost analysis of a base case MTR membrane CO{sub 2} capture system retrofitted to the AEP Conesville Unit 5 boiler. Some of the key findings from this study and a sensitivity analysis performed by MTR include: The MTR membrane process can capture 90% of the CO{sub 2} in coal flue gas and produce high-purity CO{sub 2} (>99%) ready for sequestration. CO{sub 2} recycle to the boiler appears feasible with minimal impact on boiler performance; however, further study by a boiler OEM is recommended. For a membrane process built today using a combination of slight feed compression, permeate vacuum, and current compression equipment costs, the membrane capture process can be competitive with the base case MEA process at 90% CO{sub 2} capture from a coal-fired power plant. The incremental LCOE for the base case membrane process is about equal to that of a base case MEA process, within the uncertainty in the analysis. With advanced membranes (5,000 gpu for CO{sub 2} and 50 for CO{sub 2}/N{sub 2}), operating with no feed compression and

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

2012-03-31T23:59:59.000Z

248

Using Flue Gas Huff 'n Puff Technology and Surfactants to Increase Oil Production from the Antelope Shale Formation of the Railroad Gap Oil Field  

Science Conference Proceedings (OSTI)

This project was designed to test cyclic injection of exhaust flue gas from compressors located in the field to stimulate production from Antelope Shale zone producers. Approximately 17,000 m{sup 3} ({+-}600 MCF) of flue gas was to be injected into each of three wells over a three-week period, followed by close monitoring of production for response. Flue gas injection on one of the wells would be supplemented with a surfactant.

McWilliams, Michael

2001-12-18T23:59:59.000Z

249

Desulfurization of fuel gases in fluidized bed gasification and hot fuel gas cleanup systems  

DOE Patents (OSTI)

A problem with the commercialization of fluidized bed gasification is that vast amounts of spent sorbent are generated if the sorbent is used on a once-through basis, especially if high sulfur coals are burned. The requirements of a sorbent for regenerative service in the FBG process are: (1) it must be capable of reducing the sulfur containing gas concentration of the FBG flue gas to within acceptable environmental standards; (2) it must not lose its reactivity on cyclic sulfidation and regeneration; (3) it must be capable of regeneration with elimination of substantially all of its sulfur content; (4) it must have good attrition resistance; and, (5) its cost must not be prohibitive. It has now been discovered that calcium silicate pellets, e.g., Portland cement type III pellets meet the criteria aforesaid. Calcium silicate removes COS and H/sub 2/S according to the reactions given to produce calcium sulfide silicate. The sulfur containing product can be regenerated using CO/sub 2/ as the regenerant. The sulfur dioxide can be conveniently reduced to sulfur with hydrogen or carbon for market or storage. The basic reactions in the process of this invention are the reactions with calcium silicate given in the patent. A convenient and inexpensive source of calcium silicate is Portland cement. Portland cement is a readily available, widely used construction meterial.

Steinberg, M.; Farber, G.; Pruzansky, J.; Yoo, H.J.; McGauley, P.

1983-08-26T23:59:59.000Z

250

A Low Cost and High Efficient Facility for Removal of $\\SO_{2}$ and $\\NO_{x}$ in the Flue Gas from Coal Fire Power Plant  

E-Print Network (OSTI)

A Low Cost and High Efficient Facility for Removal of $\\SO_{2}$ and $\\NO_{x}$ in the Flue Gas from Coal Fire Power Plant

Pei, Y J; Dong, X; Feng, G Y; Fu, S; Gao, H; Hong, Y; Li, G; Li, Y X; Shang, L; Sheng, L S; Tian, Y C; Wang, X Q; Wang, Y; Wei, W; Zhang, Y W; Zhou, H J

2001-01-01T23:59:59.000Z

251

Compression stripping of flue gas with energy recovery  

SciTech Connect

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

252

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

253

Improved Recovery from Gulf of Mexico Reservoirs, Volume 4, Comparison of Methane, Nitrogen and Flue Gas for Attic Oil. February 14, 1995 - October 13, 1996. Final Report  

SciTech Connect

Gas injection for attic oil recovery was modeled in vertical sandpacks to compare the process performance characteristics of three gases, namely methane, nitrogen and flue gas. All of the gases tested recovered the same amount of oil over two cycles of gas injection. Nitrogen and flue gas recovered oil more rapidly than methane because a large portion of the methane slug dissolved in the oil phase and less free gas was available for oil displacement. The total gas utilization for two cycles of gas injection was somewhat better for nitrogen as compared to methane and flue gas. The lower nitrogen utilization was ascribed to the lower compressibility of nitrogen.

Wolcott, Joanne; Shayegi, Sara

1997-01-13T23:59:59.000Z

254

Summary and assessment of METC zinc ferrite hot coal gas desulfurization test program, final report: Volume 2, Appendices  

Science Conference Proceedings (OSTI)

The Morgantown Energy Technology Center (METC) has conducted a test program to develop a zinc ferrite-based high temperature desulfurization process which could be applied to fuel gas entering downstream components such as molten carbonate fuel cells or gas turbines. As a result of prior METC work with iron oxide and zinc oxide sorbents, zinc ferrite evolved as a candidate with the potential for high capacity, low equilibrium levels of H/sub 2/S, and structural stability after multiple regenerations. The program consisted of laboratory-scale testing with a two-inch diameter reactor and simulated fixed-bed gasifier gas; bench-scale testing with a six-inch diameter reactor and actual gas from the METC 42-inch fixed bed gasifier; as well as laboratory-scale testing of zinc ferrite with simulated fluidized bed gasifier gas. Data from sidestream testing are presented. 18 refs.

Underkoffler, V.S.

1986-12-01T23:59:59.000Z

255

Hot coal gas desulfurization with manganese-based sorbents. Quarterly report, October--December 1993  

SciTech Connect

The focus of work being performed on Hot Coal Gas Desulfurization at the Morgantown Energy Technology Center is primarily in the use of zinc ferrite and zinc titanate sorbents; however, prior studies indicated that an alternate sorbent, manganese dioxide-containing ore in mixture with alumina (75 wt% ore + 25 wt% Al{sub 2}O{sub 3}) may be a viable alternative to zinc-based sorbents. Manganese, for example, has a lower vapor pressure in the elemental state than zinc hence it is not as likely to undergo depletion from the sorbent surface upon loading and regeneration cycles. Also manganese oxide is less readily reduced to the elemental state than iron hence the range of reduction potentials for oxygen is somewhat greater than for zinc ferrite. In addition, thermodynamic analysis of the manganese-oxygen-sulfur system shows it to be less amenable to sulfation than zinc ferrite. Potential also exists for utilization of manganese at higher temperatures than zinc ferrite or zinc titanate. This Fifth Quarterly Report documents progress in pellet testing via thermogravimetric analysis of pellet formulation FORM4-A of a manganese ore/alumina combination. This formulation, described more fully in the Quarterly Technical Progress Report of October 15, 1993, consists of manganese carbonate combined with alundum. A 2-inch fixed-bed reactor has been fabricated and is now ready for subjecting pellets to cyclic loading and regeneration; however, a minor problem has arisen during the regeneration cycle in that sulfur tends to form and plug the exit tube during the early stage of regeneration. This problem is about to be overcome by increasing the flow rate of air during the regeneration cycle resulting in more oxidizing conditions and hence less tendency for sulfide sulfur (S{sup =}) to oxidize to the intermediate elemental form (S{sup o}) rather than to 4-valent (S{sup +4}).

Hepworth, M.T.; Slimane, R.B.

1994-01-01T23:59:59.000Z

256

Process to recover CO/sub 2/ from flue gas gets first large-scale tryout in Texas  

SciTech Connect

This article describes a new plant that will recover 1,120 tons/day of CO/sub 2/ for use in an enhanced oil recovery (EOR) project in West Texas. Feed for the plant is flue gas from an adjacent electrical power generating station. Product CO/sub 2/ is pipelined from the recovery plant in a supercritical state at about 2,000 psig. The pilot plant demonstrated the ability of Dow Chemical's Gas Spec amine solvent to recover CO/sub 2/ from industrial flue gas, and confirmed that Procon/Dow's improved solvent adsorption system is effective in reducing the energy requirements.

St. Clair, J.H.; Simister, W.F.

1983-02-14T23:59:59.000Z

257

Flue Gas Conditioning to Reduce Particulate Emissions in Industrial Coal-Fired Boilers  

E-Print Network (OSTI)

Chemical technology has been used successfully to solve many of the operational and emissions problems that result from burning coal. This paper describes the use of blended chemical flue gas conditioners to significantly reduce particulate emissions in coal-fired industrial boilers. In many cases, these chemical conditioning agents have increased the efficiency of electrostatic precipitators and mechanical collectors by more than fifty percent. The effectiveness of this technology has been demonstrated on units generating 50,000 to 200,000 lbs./hr. steam. Results achieved at various industrial plants under actual operating conditions are presented.

Miller, B.; Keon, E.

1980-01-01T23:59:59.000Z

258

Reactive carbon from life support wastes for incinerator flue gas cleanup-System Testing  

DOE Green Energy (OSTI)

This paper presents the results from a joint research initiative between NASA Ames Research Center and Lawrence Berkeley National lab. The objective of the research is to produce activated carbon from life support wastes and to use the activated carbon to adsorb and chemically reduce the NO{sub x} and SO{sub 2} contained in incinerator flue gas. Inedible biomass waste from food production is the primary waste considered for conversion to activated carbon. Results to date show adsorption of both NO{sub x} and SO{sub 2} in activated carbon made from biomass. Conversion of adsorbed NO{sub x} to nitrogen has also been observed.

Fisher, John W.; Pisharody, Suresh; Moran, Mark J.; Wignarajah, Kanapathipillai; Xu, X.H.; Shi, Yao; Chang, Shih-Ger

2002-05-14T23:59:59.000Z

259

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

SciTech Connect

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

260

Carbon Dioxide Removal from Flue Gas Using Microporous Metal Organic Frameworks  

SciTech Connect

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

Note: This page contains sample records for the topic "flue gas desulfurization" 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

Fundamental mechanisms in flue gas conditioning. Quarterly report, October 1994--December 1994  

Science Conference Proceedings (OSTI)

This project is divided into four tasks. We developed our Management Plan in Task 1. Task 2, Evaluation of Mechanisms in FGD Sorbent and Ash Interactions, focused on characteristics of binary mixtures of these distinct powders. Task 3, Evaluation of Mechanisms in Conditioning Agents and Ash, was designed to examine effects of various conditioning agents on fine ash particles to determine mechanisms by which these agents alter physical properties of ash. We began Tasks 2 and 3 with an extensive literature search and assembly of existing theories. We completed this phase of the project with publication of two special Topical Reports. During the next phase of the project we analyzed a variety of fly ashes and fine powders in the laboratory. Pilot-scale evaluations were then performed to verify the results we obtained in these laboratory analyses. Under Task 4 we will issue our Final Report that will summarize the results of our laboratory and pilot-scale work and will also include a Flue Gas Conditioning Model. In our literature reviews reported in Topical Reports 1 and 2, we emphasized the roles adsorbed water can have in controlling bulk properties of powders. The experiments we performed were primarily designed to define the extent to which water affects key properties of ashes, powders, and mixtures of sorbents and ashes. We have recently completed a series of pilot-scale tests designed to determine the effects that adsorbed water has on fabric filtration and electrostatic precipitation of entrained fly ash particles in actual flue gas environments.

Snyder, T.R.

1995-01-16T23:59:59.000Z

262

Mercury Speciation in Coal-Fired Power Plant Flue Gas-Experimental Studies and Model Development  

SciTech Connect

The overall goal of the project was to obtain a fundamental understanding of the catalytic reactions that are promoted by solid surfaces present in coal combustion systems and develop a mathematical model that described key phenomena responsible for the fate of mercury in coal-combustion systems. This objective was achieved by carefully combining laboratory studies under realistic process conditions using simulated flue gas with mathematical modeling efforts. Laboratory-scale studies were performed to understand the fundamental aspects of chemical reactions between flue gas constituents and solid surfaces present in the fly ash and their impact on mercury speciation. Process models were developed to account for heterogeneous reactions because of the presence of fly ash as well as the deliberate addition of particles to promote Hg oxidation and adsorption. Quantum modeling was used to obtain estimates of the kinetics of heterogeneous reactions. Based on the initial findings of this study, additional work was performed to ascertain the potential of using inexpensive inorganic sorbents to control mercury emissions from coal-fired power plants without adverse impact on the salability fly ash, which is one of the major drawbacks of current control technologies based on activated carbon.

Radisav Vidic; Joseph Flora; Eric Borguet

2008-12-31T23:59:59.000Z

263

Mercury Control Research: Effects of Fly Ash and Flue Gas Parameters on Mercury Speciation  

E-Print Network (OSTI)

and fly ash parameters on the oxidation of HgOin simulated flue gases containing hydrogen chloride (Hel-combustion region are unknown, and the major reaction pathways for Hg oxidation in combustion flue gases remain in the oxidation ofHgo in flue gases containingHC!. Thus, an important parameter that influences the oxidation of

Columbia University

264

Hollow fiber adsorbents for CO{sub 2} removal from flue gas  

Science Conference Proceedings (OSTI)

The nation's pulverized coal infrastructure is aging, and implementation of current retrofit postcombustion capture methods is extremely expensive. This paper describes a technology based on hollow polymeric fibers with sorbent particles embedded in the porous fiber wall to enable postcombustion CO{sub 2} capture via a rapid temperature swing adsorption (RTSA) system. The system takes advantage of the hollow fiber morphology by passing cooling water through the bores during sorption to maximize sorption capacities and steam through the bores during desorption to desorb CO{sub 2} efficiently. The thin-walled hollow fibers offer the advantage of rapid heat and mass transport. To avoid mass transfer between the core and the fiber sheath, a dense lumen layer is used on the interior of the fiber wall. This system has advantages over competing technologies. Specifically, the fiber sorbent contactor minimizes flue gas pressure drop across the bed, while maximizing sorption efficiencies via rapid thermal cycles and low regenerative thermal requirements.

Lively, R.P.; Chance, R.R.; Kelley, B.T.; Deckman, H.W.; Drese, J.H.; Jones, C.W.; Koros, W.J. [Georgia Institute of Technology, Atlanta, GA (United States)

2009-08-15T23:59:59.000Z

265

By-product disposal from MSW incinerator flue gas cleaning systems  

Science Conference Proceedings (OSTI)

Waste incineration has been found to be an effective method of achieving significant volume reduction of Municipal Solid Waste (MSW) while at the same time allowing for energy recovery in the form of steam or electricity. Concern over potential air pollution from incinerators in the form of acid gases, heavy metals and dioxins has led to the application of Spray Dryer Absorption (SDA) flue gas cleaning systems to control these emissions. SDA has demonstrated high efficiencies in converting these air pollutants into a dry by-product for disposal. This has, in turn, led to concerns over potential secondary pollution from the disposal of these by-products. This paper presents a description of the SDA process and reviews disposal options for the SDA product. Product characteristics are given and results of leaching studies are presented. Comparisons between EPA's and TEP and TCLP procedures are presented. Results of dioxin measurements from the by-product are given.

Donnelly, J.R. (Joy Manufacturing Co., Los Angeles, CA (US)); Jons, E. (A/S Niro Atomizer, Copenhagen (DK))

1987-01-01T23:59:59.000Z

266

Fundamental mechanisms in flue gas conditioning. Quarterly report, April--June 1994  

Science Conference Proceedings (OSTI)

This project is divided into four tasks. The author developed a Management Plan in Task 1. Task 2, Evaluation of Mechanisms in FGD Sorbent and Ash Interactions, focuses on characteristics of binary mixtures of these distinct powders. Task 3, Evaluation of Mechanisms in Conditioning Agents and Ash, is designed to examine effects of various conditioning agents on fine ash particles to determine mechanisms by which these agents alter physical properties of ash. The author began Tasks 2 and 3 with an extensive literature search and assembly of existing theories. He completed this phase of the project with publication of two special Topical Reports. During the past several quarters he performed analyses of the samples in the database. Pilot-scale evaluations have begun and will continue through the next two quarters. The author will include the results of laboratory and pilot-scale work performed under Tasks 2 and 3 in a Flue Gas Conditioning Model that will be issued under Task 4. The Final Report for the project will also be prepared under Task 4. In the literature reviews reported in Topical Reports 1 and 2, the author emphasized the roles adsorbed water can have in controlling bulk properties of powders. The experiments performed were primarily designed to define the extent to which water affects key properties of ashes, powders, and mixtures of sorbents and ashes. The author is currently performing a series of pilot-scale tests designed to determine the effects that absorbed water has on fabric filtration and electrostatic precipitation of entrained fly ash particles in actual flue gas environments.

Snyder, T.R.

1994-07-12T23:59:59.000Z

267

Executive Summary of the Inventory of U.S. Greenhouse Gas Emissions and Sinks: 19902009 1 n emissions inventory that identifies and quantifies a country's primary anthropogenic1  

E-Print Network (OSTI)

stone, flue gas desulfurization, and glass manufacturing), soda ash production and consumption, titaniumExecutive Summary of the Inventory of U.S. Greenhouse Gas Emissions and Sinks: 1990­2009 1 n, in accordance with the relevant provisions of the Convention, stabilization of greenhouse gas concentrations

Little, John B.

268

Decarb/Desal: Separation of Carbon Dioxide from Flue Gas with Simultaneous Fresh Water Production  

Science Conference Proceedings (OSTI)

If fossil fuels continue to be a major part of the world's energy supply, effective means must be developed to deal with the carbon emissions. Geologic sequestration of supercritical CO{sub 2} is expected to play a major role in mitigating this problem. Separating carbon dioxide from other gases is the most costly aspect of schemes for geologic sequestration. That cost is driven by the complexity and energy intensity of current chemical-stripping methods for separating carbon dioxide. Our experience in water treatment technology indicated that an entirely new approach could be developed, taking advantage of water's propensity to separate gases that ionize in water (like CO{sub 2}) from those that do not (like N{sub 2}). Even though water-based systems might not have the extreme selectivity of chemicals like substituted amines used in industrial systems today, they have the potential to tolerate NO{sub x}, SO{sub x}, and particulates while also producing clean drinking water as a valuable byproduct. Lower capital cost, broader range of applicability, environmental friendliness, and revenue from a second product stream give this approach the potential to significantly expand the worldwide application of carbon separation for geologic sequestration. Here we report results for separation of CO{sub 2} from flue gas by two methods that simultaneously separate carbon dioxide and fresh water: ionic pumping of carbonate ions dissolved in water, and thermal distillation. The ion pumping method dramatically increases dissolved carbonate ion in solution and hence the overlying vapor pressure of CO{sub 2} gas, allowing its removal as a pure gas. We have used two common water treatment methods to drive the ion pumping approach, reverse osmosis and electrodialysis to produce pure CO{sub 2}. This novel approach to increasing the concentration of the extracted gas permits new approaches to treating flue gas, because the slightly basic water used as the extraction medium is impervious to trace acid gases that destroy existing solvents, and no pre-separation is necessary. Thermal distillation uses boiling water to steam strip solid sorbents - the steam is recovered as fresh water. We anticipate that our method will compete favorably with current chemical stripping systems used for CO{sub 2} separation at power plants, which incur a 35% energy penalty. Thus we expect to offer a dramatically improved solution for removing carbon from hydrocarbon combustion. Our method can be demonstrated on small sources, which will enable us to conduct the demonstrations required to build confidence in the method. If successful, we will be in a position to advance a follow-on proposal for a demonstration at the 10-MW scale.

Aines, R; Bourcier, W

2009-10-21T23:59:59.000Z

269

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

SciTech Connect

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

270

Desulfurization of hot fuel gas produced from high-chlorine Illinois coals. Final technical report, September 1, 1991--August 31, 1992  

SciTech Connect

In this project, simulated gasifier-product streams were contacted with the zinc titanate desulfurization sorbent in a bench-scale atmospheric fluidized-bed reactor at temperatures ranging from 538 to 750 {degree}C (1000 to 1382 {degree}F). The first set of experiments involved treating a medium-Btu fuel gas (simulating that of a ``Texaco`` oxygen-blown, entrained-bed gasifier) containing 1.4 percent H{sub 2}S and HCl concentrations of 0, 200, and 1500 ppmv. The second experimental set evaluated hot-gas desulfurization of a low-Btu fuel gas (simulating the product of the ``U-Gas`` air-blown gasifier), with HCl concentrations of 0, 200, and 800 ppmv. These operating conditions were typical of the gas-treatment requirements of gasifiers fueled by Illinois basin coals containing up to 0.6 percent chlorine. The results of the experiments at 538 and 650 {degree}C at all the HCl concentrations revealed no deleterious effects on the capability of the sorbent to remove H{sub 2}S from the fuel gas mixtures. In most cases, the presence of the HCl significantly enhanced the desulfurization reaction rate. Some zinc loss, however, was encountered in certain situations at 750 {degree}C when low-steam operating conditions were present. Also of interest, a portion of the incoming HCl was removed from the gas stream and was retained permanently by the sorbent. This behavior was examined in more detail in a limited set of experiments aimed at identifying ways to modify the sorbents composition so that the sorbent could act as a simultaneous desulfurization and dechlorination agent in the hot-gas cleanup process.

O`Brien, W.S. [Southern Illinois Univ., Carbondale, IL (United States); Gupta, R.P. [Research Triangle Inst., Research Triangle Park, NC (United States)

1992-12-31T23:59:59.000Z

271

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

Science Conference Proceedings (OSTI)

The U.S. Department of Energy and ADA Environmental Solutions have begun 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 flyash. There is a need to provide cost-effective and safer alternatives to traditional flue gas conditioning with SO{sub 3} and ammonia. During the second reporting quarter for this project, design and development is continuing on an electrostatic tensiometer to measure cohesion of flyash layers. A dedicated test fixture to automate flyash electrical resistivity testing is also underway. Ancillary instrumentation to control gas humidification within these test fixtures is also under construction.

Kenneth E. Baldrey

2000-09-01T23:59:59.000Z

272

Management of dry flue gas desulfurization by-products in underground mines. Annual report, October 1993--September 1994  

Science Conference Proceedings (OSTI)

Preliminary environmental risk assessment on the FGD by-products to be placed underground is virtually complete. The initial mixes for pneumatic and hydraulic placement have been selected and are being subject to TCLP, ASTM, and modified SLP shake tests as well as ASTM column leaching. Results of these analyses show that the individual coal combustion residues, and the residues mixes, are non-hazardous in character. Based on available information, including well logs obtained from Peabody Coal Company, a detailed study of the geology of the placement site was completed. The study shows that the disposal site in the abandoned underground mine workings at depths of between 325 and 375 feet are well below potable groundwater resources. This, coupled with the benign nature of the residues and residues mixtures, should alleviate any concern that the underground placement will have adverse effects on groundwater resources. Seven convergence stations were installed in the proposed underground placement area of the Peabody Coal Company No. 10 mine. Several sets of convergence data were obtained from the stations. A study of materials handling and transportation of coal combustion residues from the electric power plant to the injection site has been made. The study evaluated the economics of the transportation of coal combustion residues by pneumatic trucks, by pressure differential rail cars, and by SEEC, Inc. collapsible intermodal containers (CICs) for different annual handling rates and transport distances. The preliminary physico-chemical characteristics and engineering properties of various FBC fly ash-spent bed mixes have been determined, and long-term studies of these properties are continuing.

Chugh, Y.P.; Dutta, D.; Esling, S.; Ghafoori, N.; Paul, B.; Sevim, H.; Thomasson, E.

1994-10-01T23:59:59.000Z

273

Demonstration/evaluation of the Cat-Ox flue gas desulfurization system. Final report, June 1970-October 1975  

SciTech Connect

The report gives a comprehensive summary of the experience gained and the problems encountered during the Cat-Ox demonstration program. The report outlines the process design and construction, as well as operating experience and problems. Test results and conclusions derived from baseline testing, acceptance testing, ESP testing, transient testing, and a number of special tests and studies associated with the system are reported.

Bee, R.; Reale, R.; Wallo, A.

1978-03-01T23:59:59.000Z

274

Management of dry flue gas desulfurization by-products in underground mines. Quarterly report, August 1--October 31, 1997  

Science Conference Proceedings (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

275

Refuse Composition And flue-Gas Analyses from Mun;c;pal  

E-Print Network (OSTI)

(see Figure 3 and 4). In the fixed-bed or moving-bed process, the pollutant-loaded flue gases in the flue gases which occur during combustion and total approx. 350,000 m3(STP, dryt/hr is separatedReduction in Mercury Emissions with Lignite Coke W. Esser-Schmittmann, J. Wirling and U. Lenz Due

Columbia University

276

CO2 separation from flue gas using hollow fiber membrane contactors  

NLE Websites -- All DOE Office Websites (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.

277

Flue-gas carbon capture on carbonaceous sorbents: Toward a low-cost multifunctional Carbon Filter for 'Green' energy producers  

SciTech Connect

A low-pressure Carbon Filter Process (patent pending) is proposed to capture carbon dioxide (CO{sub 2}) from flue gas. This filter is filled with a low-cost carbonaceous sorbent, such as activated carbon or charcoal, which has a high affinity (and, hence, high capacity) to CO{sub 2} but not to nitrogen (N{sub 2}). This, in turn, leads to a high CO{sub 2}/N{sub 2} selectivity, especially at low pressures. The Carbon Filter Process proposed in this work can recover at least 90% of flue-gas CO{sub 2} of 90%+ purity at a fraction of the cost normally associated with the conventional amine absorption process. The Carbon Filter Process requires neither expensive materials nor flue-gas compression or refrigeration, and it is easy to heat integrate with an existing or grassroots power plant without affecting the cost of the produced electricity too much. An abundant supply of low-cost CO{sub 2} from electricity producers is good news for enhanced oil recovery (EOR) and enhanced coal-bed methane recovery (ECBMR) operators, because it will lead to higher oil and gas recovery rates in an environmentally sensitive manner. A CO{sub 2}-rich mixture that contains some nitrogen is much less expensive to separate from flue-gas than pure CO{sub 2}; therefore, mixed CO{sub 2}/N{sub 2}-EOR and CO{sub 2}/N{sub 2}-ECBMR methods are proposed to maximize the overall carbon capture and utilization efficiency.

Radosz, M.; Hu, X.D.; Krutkramelis, K.; Shen, Y.Q. [University of Wyoming, Laramie, WY (United States)

2008-05-15T23:59:59.000Z

278

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

SciTech Connect

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

279

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

SciTech Connect

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

280

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

SciTech Connect

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, progress was made in obtaining an industry partner for a long-term demonstration and in technology transfer activities. Engineering and equipment procurement activities related to the long-term demonstration were also completed.

Kenneth E. Baldrey

2001-10-01T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" from the National Library of EnergyBeta (NLEBeta).
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281

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

NLE Websites -- All DOE Office Websites (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

282

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

Science Conference Proceedings (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

283

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

Science Conference Proceedings (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

284

Fundamental mechanisms in flue gas conditioning. Quarterly report, January 1992--March 1992  

Science Conference Proceedings (OSTI)

This project is divided into four tasks. The Management Plan was developed in task 1. Task 2, Evaluation of Mechanisms in FGD Sorbent and Ash Interactions, focuses on the characteristics of binary mixtures of these distinct powders. Task 3, Evaluation of Mechanisms in Conditioning Agents and Ash, is designed to examine the effects of various conditioning agents on fine ash particles to determine the mechanisms by which these agents alter the physical properties of the ash. Tasks 2 and 3 began with an extensive literature search and the assembly of existing theories. This phase of the project is now complete. During the past quarter, initial preparations of laboratory equipment for laboratory testing have been made. A plan for initial laboratory tests has been submitted to the Project Manager for review. Laboratory testing will commence once these laboratory plans have been formally approved. The results of the work performed under task 2 and 3 will be included in a Flue Gas Conditioning Model that will be issued under task 4. The Final Report for the project will also be prepared under task 4.

Snyder, T.R.; Robinson, M.S.; Bush, P.V.

1992-04-27T23:59:59.000Z

285

Fundamental mechanisms in flue gas conditioning. Quarterly report, September 1991--December 1991  

Science Conference Proceedings (OSTI)

This project is divided into four tasks. Task 1 is the Development of a Management Plan. Task 2, Evaluation of Mechanisms in FGD Sorbent and Ash Interactions, focuses on the characteristics of binary mixtures of these distinct powders. Task 3, Evaluation of Mechanisms in Conditioning Agents and Ash, is designed to examine the effects of various conditioning agents on fine ash particles to determine the mechanisms by which these agents alter the physical properties of the ash. Tasks 2 and 3 began with an extensive literature search and the assembly of existing theories. The results of the work performed under Tasks 2 and 3 will be included in a Flue Gas Conditioning Model that will be issued under Task 4. The Final Report for the project will also be prepared under Task 4. This quarterly report covers four months in order to synchronize the reporting periods for this project with US Government quarters. Work performed on the project during the past quarter consisted almost entirely of the review of literature pertaining to the objectives of Tasks 2 and 3. The primary results of that review are discussed at length in Topical Reports 1 and 2, submitted January 9, 1992. As a consequence of the work described in the topical reports, several of the project`s Measures of Success that were described in the first quarterly report have been achieved. This quarterly report will discuss these achievements.

Snyder, T.R.

1992-01-23T23:59:59.000Z

286

Evaluation of BOC'S Lotox Process for the Oxidation of Elemental Mercury in Flue Gas from a Coal-Fired Boiler  

SciTech Connect

Linde's Low Temperature Oxidation (LoTOx{trademark}) process has been demonstrated successfully to remove more than 90% of the NOx emitted from coal-fired boilers. Preliminary findings have shown that the LoTOx{trademark} process can be as effective for mercury emissions control as well. In the LoTOx{trademark} system, ozone is injected into a reaction duct, where NO and NO{sub 2} in the flue gas are selectively oxidized at relatively low temperatures and converted to higher nitrogen oxides, which are highly water soluble. Elemental mercury in the flue gas also reacts with ozone to form oxidized mercury, which unlike elemental mercury is water-soluble. Nitrogen oxides and oxidized mercury in the reaction duct and residual ozone, if any, are effectively removed in a wet scrubber. Thus, LoTOx{trademark} appears to be a viable technology for multi-pollutant emission control. To prove the feasibility of mercury oxidation with ozone in support of marketing LoTOx{trademark} for multi-pollutant emission control, Linde has performed a series of bench-scale tests with simulated flue gas streams. However, in order to enable Linde to evaluate the performance of the process with a flue gas stream that is more representative of a coal-fired boiler; one of Linde's bench-scale LoTOx{trademark} units was installed at WRI's combustion test facility (CTF), where a slipstream of flue gas from the CTF was treated. The degree of mercury and NOx oxidation taking place in the LoTOx{trademark} unit was quantified as a function of ozone injection rates, reactor temperatures, residence time, and ranks of coals. The overall conclusions from these tests are: (1) over 80% reduction in elemental mercury and over 90% reduction of NOx can be achieved with an O{sub 3}/NO{sub X} molar ratio of less than two, (2) in most of the cases, a lower reactor temperature is preferred over a higher temperature due to ozone dissociation, however, the combination of both low residence time and high temperature proved to be effective in the oxidation of both NOx and elemental mercury, and (3) higher residence time, lower temperature, and higher molar ratio of O{sub 3}/NOx contributed to the highest elemental mercury and NOx reductions.

Khalid Omar

2008-04-30T23:59:59.000Z

287

CO{sub 2} Capture Membrane Process for Power Plant Flue Gas  

Science Conference Proceedings (OSTI)

Because the fleet of coal-fired power plants is of such importance to the nationâ??s energy production while also being the single largest emitter of CO{sub 2}, the development of retrofit, post-combustion CO{sub 2} capture technologies for existing and new, upcoming coal power plants will allow coal to remain a major component of the U.S. energy mix while mitigating global warming. Post-combustion carbon capture technologies are an attractive option for coal-fired power plants as they do not require modification of major power-plant infrastructures, such as fuel processing, boiler, and steam-turbine subsystems. In this project, the overall objective was to develop an advanced, hollow-fiber, polymeric membrane process that could be cost-effectively retrofitted into current pulverized coal-fired power plants to capture at least 90% of the CO{sub 2} from plant flue gas with 95% captured CO{sub 2} purity. The approach for this project tackled the technology development on three different fronts in parallel: membrane materials R&D, hollow-fiber membrane module development, and process development and engineering. The project team consisted of RTI (prime) and two industrial partners, Arkema, Inc. and Generon IGS, Inc. Two CO{sub 2}-selective membrane polymer platforms were targeted for development in this project. For the near term, a next-generation, high-flux polycarbonate membrane platform was spun into hollow-fiber membranes that were fabricated into both lab-scale and larger prototype (~2,200 ft{sup 2}) membrane modules. For the long term, a new fluoropolymer membrane platform based on poly(vinylidene fluoride) [PVDF] chemistry was developed using a copolymer approach as improved capture membrane materials with superior chemical resistance to flue-gas contaminants (moisture, SO{sub 2}, NOx, etc.). Specific objectives were: ï?· Development of new, highly chemically resistant, fluorinated polymers as membrane materials with minimum selectivity of 30 for CO{sub 2} over N{sub 2} and CO{sub 2} permeance greater than 300 gas permeation units (GPU) targeted; ï?· Development of next-generation polycarbonate hollow-fiber membranes and membrane modules with higher CO{sub 2} permeance than current commercial polycarbonate membranes; ï?· Development and fabrication of membrane hollow fibers and modules from candidate polymers; ï?· Development of a CO{sub 2} capture membrane process design and integration strategy suitable for end-of-pipe, retrofit installation; and ï?· Techno-economic evaluation of the "best" integrated CO{sub 2} capture membrane process design package In this report, the results of the project research and development efforts are discussed and include the post-combustion capture properties of the two membrane material platforms and the hollow-fiber membrane modules developed from them and the multi-stage process design and analysis developed for 90% CO{sub 2} capture with 95% captured CO{sub 2} purity.

Lora Toy; Atish Kataria; Raghubir Gupta

2011-09-30T23:59:59.000Z

288

Hot-gas desulfurization. II. Use of gasifier ash in a fluidized-bed process. Final report  

DOE Green Energy (OSTI)

Three gasifier coal ashes were used as reactant/sorbents in batch fluidized-beds to remove hydrogen sulfide from hot, made-up fuel gases. It is predominantly the iron oxide in the ash that reacts with and removes the hydrogen sulfide; the sulfur reappears in ferrous sulfide. Sulfided ashes were regenerated by hot, fluidizing streams of oxygen in air; the sulfur is recovered as sulfur dioxide, exclusively. Ash sorption efficiency and sulfur capacity increase and stabilize after several cycles of use. These two parameters vary directly with the iron oxide content of the ash and process temperature, but are independent of particle size in the range 0.01 - 0.02 cm. A western Kentucky No. 9 ash containing 22 weight percent iron as iron oxide sorbed 4.3 weight percent sulfur at 1200/sup 0/F with an ash sorption efficiency of 0.83 at ten percent breakthrough. A global, fluidized-bed, reaction rate model was fitted to the data and it was concluded that chemical kinetics is the controlling mechanism with a predicted activation energy of 19,600 Btu/lb mol. Iron oxide reduction and the water-gas-shift reaction were two side reactions that occurred during desulfurization. The regeneration reaction occurred very rapidly in the fluid-bed regime, and it is suspected that mass transfer is the controlling phenomenon.

Schrodt, J.T.

1981-02-01T23:59:59.000Z

289

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

SciTech Connect

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

290

Development of Novel CO2 Adsorbents for Capture of CO2 from Flue Gas  

SciTech Connect

Capturing CO2 emissions generated from fossil fuel-based power plants has received widespread attention and is considered a vital course of action for CO2 emission abatement. Efforts are underway at the Department of Energy’s National Energy Technology Laboratory to develop viable energy technologies enabling the CO2 capture from large stationary point sources. Solid, immobilized amine sorbents (IAS) formulated by impregnation of liquid amines within porous substrates are reactive towards CO2 and offer an alternative means for cyclic capture of CO2 eliminating, to some degree, inadequacies related to chemical absorption by aqueous alkanolamine solutions. This paper describes synthesis, characterization, and CO2 adsorption properties for IAS materials previously tested to bind and release CO2 and water vapor in a closed loop life support system. Tetraethylenepentamine (TEPA), acrylonitrile-modified tetraethylenepentamine (TEPAN), and a single formulation consisting of TEPAN and N, N’-bis(2-hydroxyethyl)ethylenediamine (BED) were individually supported on a poly (methyl methacrylate) (PMMA) substrate and examined. CO2 adsorption profiles leading to reversible CO2 adsorption capacities were obtained using thermogravimetry. Under 10% CO2 in nitrogen at 25°C and 1 atm, TEPA supported on PMMA over 60 minutes adsorbed ~3.2 mmol/g{sorbent} whereas, TEPAN supported on PMMA along with TEPAN and BED supported on PMMA adsorbed ~1.7 mmol/g{sorbent} and ~2.3 mmol/g{sorbent} respectively. Cyclic experiments with a 1:1 weight ratio of TEPAN and BED supported on poly (methyl methacrylate) beads utilizing a fixed-bed flow system with 9% CO2, 3.5% O2, nitrogen balance with trace gas constituents were studied. CO2 adsorption capacity was ~ 3 mmols CO2/g{sorbent} at 40°C and 1.4 atm. No beneficial effect on IAS performance was found using a moisture-laden flue gas mixture. Tests with 750 ppmv NO in a humidified gas stream revealed negligible NO sorption onto the IAS. A high SO2 concentration resulted in incremental loss in IAS performance and revealed progressive degrees of “staining” upon testing. Adsorption of SO2 by the IAS necessitates upstream removal of SO2 prior to CO2 capture.

Fauth, D.J.; Filburn, T.P. (University of Hartford, West Hartford, CT); Gray, M.L.; Hedges, S.W.; Hoffman, J.; Pennline, H.W.; Filburn, T.

2007-06-01T23:59:59.000Z

291

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

Science Conference Proceedings (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

292

LIFAC Sorbent Injection Desulfurization Demonstration Project...  

NLE Websites -- All DOE Office Websites (Extended Search)

of the flue gas in a separate activation reactor, which increases SO 2 removal. An electrostatic precipitator downstream from the point of injection captures the reaction...

293

Experimental Study on the Separation of CO2 from Flue Gas Using Hollow Fiber Membrane Contactors with Aqueous Solution of Potassium Glycinate  

Science Conference Proceedings (OSTI)

Experimental study on CO2 removal from flue gas using polypropylene hollow fiber membrane contactors were conducted. Aqueous solutions of potassium glycinate were used as absorption solution to absorb CO2 in the experiments. Under moderate operating ... Keywords: Gas absorption, Carbon dioxide, Potassium glycinate, Hollow fiber membrane contactor, Membrane absorption

Weifeng Zhang; Qiuhua Wang; Mengxiang Fang; Zhongyang Luo; Kefa Cen

2009-10-01T23:59:59.000Z

294

Integrated operation of a pressurized fixed-bed gasifier, hot gas desulfurization system, and turbine simulator  

Science Conference Proceedings (OSTI)

The overall objective of the General Electric Hot Gas Cleanup (HGCU) Program is to develop a commercially viable technology to remove sulfur, particulates, and halogens from a high-temperature fuel gas stream using a moving bed, regenerable mixed metal oxide sorbent based process. The HGCU Program is based on the design and demonstration of the HGCU system in a test facility made up of a pilot-scale fixed bed gasifier, a HGCU system, and a turbine simulator in Schenectady, NY, at the General Electric Research and Development Center. The objectives of the turbine simulator testing are (1) to demonstrate the suitability of fuel gas processed by the HGCU system for use in state-of-the-art gas turbines firing at 2,350 F rotor inlet temperature and (2) to quantify the combustion characteristics and emissions on low-Btu fuel gas. The turbine simulator program also includes the development and operation of experimental combustors based on the rich-quench-lean concept (RQL) to minimize the conversion of ammonia and other fuel-bound nitrogen species to NO{sub x} during combustion. The HGCU system and turbine simulator have been designed to process approximately 8,000 lb/hr of low heating value fuel gas produced by the GE fixed bed gasifier. The HGCU system has utilized several mixed metal oxide sorbents, including zinc ferrite, zinc titanate, and Z-Sorb, with the objective of demonstrating good sulfur removal and mechanical attrition resistance as well as economic cost characteristics. Demonstration of halogen removal and the characterization of alkali and trace metal concentrations in the fuel gas are subordinate objectives of the overall program. This report describes the results of several long-duration pilot tests.

Bevan, S.; Ayala, R.E.; Feitelberg, A.; Furman, A.

1995-11-01T23:59:59.000Z

295

Method and apparatus for hot-gas desulfurization of fuel gases  

DOE Patents (OSTI)

The present invention is directed to a method and apparatus for removing sulfur values from a hot fuel gas stream in a fluidized bed contactor containing particulate sorbent material by employing a riser tube regeneration arrangement. Sulfur-laden sorbent is continuously removed from the fluidized bed through a stand pipe to the riser tube and is rapidly regenerated in the riser tube during transport of the sorbent therethrough by employing an oxygen- containing sorbent regenerating gas stream. The riser tube extends from a location below the fluidized bed to an elevation above the fluidized bed where a gas-solid separating mechanism is utilized to separate the regenerated particulate sorbent from the regeneration gases and reaction gases so that the regenerated sorbent can be returned to the fluidized bed for reuse. 3 figs., 1 tab.

Bissett, L.A.

1990-01-01T23:59:59.000Z

296

Method and apparatus for hot-gas desulfurization of fuel gases  

DOE Patents (OSTI)

The present invention is directed to a method and apparatus for removing sulfur values from a hot fuel gas stream in a fluidized bed contactor containing particulate sorbent material by employing a riser tube regeneration arrangement. Sulfur-laden sorbent is continuously removed from the fluidized bed through a stand pipe to the riser tube and is rapidly regenerated in the riser tube during transport of the sorbent therethrough by employing an oxygen- containing sorbent regenerating gas stream. The riser tube extends from a location below the fluidized bed to an elevation above the fluidized bed where a gas-solid separating mechanism is utilized to separate the regenerated particulate sorbent from the regeneration gases and reaction gases so that the regenerated sorbent can be returned to the fluidized bed for reuse. 3 figs., 1 tab.

Bissett, L.A.

1990-12-31T23:59:59.000Z

297

Selective CO2 Capture from Flue Gas Using Metal-Organic Frameworks?A Fixed Bed Study  

SciTech Connect

It is important to capture carbon dioxide from flue gas which is considered to be the main reason to cause global warming. CO2/N2 separation by novel adsorbents is a promising method to reduce CO2 emission but effect of water and CO2/N2 selectivity is critical to apply the adsorbents into practical applications. A very well known, Metal Organic Framework, NiDOBDC (Ni-MOF-74 or CPO-27-Ni) was synthesized through a solvothermal reaction and the sample (500 to 800 microns) was used in a fixed bed CO2/N2 breakthrough study with and without H2O. The Ni/DOBDC pellet has a high CO2 capacity of 3.74 mol/kg at 0.15 bar and a high CO2/N2 selectivity of 38, which is much higher than those of reported MOFs and zeolites under dry condition. Trace amount of water can impact CO2 adsorption capacity as well as CO2/N2 selectivity for the Ni/DOBDC. However, Ni/DOBDC can retain a significant CO2 capacity and CO2/N2 selectivity at 0.15 bar CO2 with 3% RH water. These results indicate a promising future to use the Ni/DOBDC in CO2 capture from flue gas.

Liu, Jian; Tian, Jian; Thallapally, Praveen K.; McGrail, B. Peter

2012-05-03T23:59:59.000Z

298

Integrated operation of a pressurized gasifier, hot gas desulfurization system and turbine simulator  

SciTech Connect

The overall objective of the General Electric Hot Gas Cleanup (HGCU) Program is to develop a commercially viable technology to remove sulfur, particulates, and halogens from a high-temperature fuel gas stream using a moving bed, regenerable mixed metal oxide sorbent based process. This technology will ultimately be incorporated into advanced Integrated Gasification Combined Cycle (IGCC) power generation systems. The objectives of the turbine simulator testing are (1) to demonstrate the suitability of fuel gas processed by the HGCU system for use in state-of-the-art gas turbines firing at F conditions (2,350 F rotor inlet temperature) and (2) to quantify the combustion characteristics and emissions of such a combustor. Testing of the GE HGCU system has been underway since December 1990. The two most recent tests, Test 5 and Test 6, represent the latest advancements in regenerator configuration, type of sorbent, and chloride control systems. Test 5 was based on the use of zinc titanate sorbent and included a revised regenerator configuration and a sodium bicarbonate injection system for chloride control. Test 6 incorporated the use of Z-Sorb, a chloride guard in the regenerator recycle loop, and further modifications to the regenerator internal configuration. This report describes the test conditions in detail and discusses the test results.

Bevan, S.; Najewicz, D.; Gal, E.; Furman, A.H.; Ayala, R.; Feitelberg, A.

1994-10-01T23:59:59.000Z

299

Anion-exchange resin-based desulfurization process. Annual technical progress report, October 1, 1992--September 30, 1993  

DOE Green Energy (OSTI)

Under the DOE Grant No. DE-FG22-90PC90309, the University of Tennessee Space Institute (UTSI) has been directed to further develop an anion-exchange, resin-based desulfurization concept that has been developed and tested on a limited scope for feasibility. From environmental as well as the economic viewpoints, it is necessary that the soluble sulfates of alkali metal sorbents be desulfurized (regenerated) and recycled to make regenerative flue gas desulfurization and MHD spent seed regeneration options more attractive. In order to achieve this, a low-temperature, low-cost desulfurization process to reactivate spent alkali metal sorbents is necessary. UTSI`s anion-exchange, resin-based concept uses the available technology and is believed to satisfy this requirement. In this DOE-sponsored project, UTSI, will perform the following investigations: Screening of commercially available resins; process variables study and improving resin performance; optimization of resin-regeneration step; evaluation of performance enhancers; development of Best-Process Schematic and related economics, and planning for proof-of-concept (POC) scale testing. The above activities have been grouped into five major tasks and the entire project is expected to take thirty-six months to complete.

Sheth, A.C.; Dharmapurikar, R.; Strevel, S.D.

1993-11-01T23:59:59.000Z

300

Flue Gas Cleanup at Temperatures about 1400 C for a Coal Fired Combined Cycle Power Plant: State and Perspectives in the Pressurized Pulverized Coal Combustion (PPCC) Project  

Science Conference Proceedings (OSTI)

The PPCC technology, a combined cycle, requires comprehensive cleaning of the flue gases because coal contains a large variety of minerals and other substances. This would lead to fast destruction of the gas turbine blades due to erosion and corrosion. The present specifications of the turbine manufacturers for the required flue gas quality are at a maximum particulate content of 5 mg/m3 s.t.p., diameter of Kraftwerke GmbH, SaarEnergie GmbH, Siemens AG, and Steag AG.

Foerster, M.E.C.; Oeking, K.; Hannes, K.

2002-09-18T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

Numerical Modeling of Reactive Multiphase Flow for FCC and Hot Gas Desulfurization Circulating Fluidized Beds  

Science Conference Proceedings (OSTI)

This work was carried out to understand the behavior of the solid and gas phases in a CFB riser. Only the riser is modeled as a straight pipe. A model with linear algebraic approximation to solids viscosity of the form, {musubs} = 5.34{epsisubs}, ({espisubs} is the solids volume fraction) with an appropriate boundary condition at the wall obtained by approximate momentum balance solution at the wall to acount for the solids recirculation is tested against experimental results. The work done was to predict the flow patterns in the CFB risers from available experimental data, including data from a 7.5-cm-ID CFB riser at the Illinois Institute of Technology and data from a 20.0-cm-ID CFB riser at the Particulate Solid Research, Inc., facility. This research aims at modeling the removal of hydrogen sulfide from hot coal gas using zinc oxide as the sorbent in a circulating fluidized bed and in the process indentifying the parameters that affect the performance of the sulfidation reactor. Two different gas-solid reaction models, the unreacted shrinking core (USC) and the grain model were applied to take into account chemical reaction resistances. Also two different approaches were used to affect the hydrodynamics of the process streams. The first model takes into account the effect of micro-scale particle clustering by adjusting the gas-particle drag law and the second one assumes a turbulent core with pseudo-steady state boundary condition at the wall. A comparison is made with experimental results.

None

2005-07-01T23:59:59.000Z

302

Choosing a coke-oven gas desulfurization system: a review of current technology  

SciTech Connect

Installation of coke-oven gas desulphurizing systems is primarily the result of air pollution control regulations. Although not currently profitable, operating costs can be minimized by choosing the technology most suited to the particular application. The Stretford Holmes, Takahax/Hirohax, Koppers Vacuum Carbonate, Sulfiban and Dravo/Still processes are discussed, together with criteria for economic analysis based on technical and by-product market evaluations.

Lynch, P.A.

1982-12-01T23:59:59.000Z

303

Fouling reduction characteristics of a no-distributor-fluidized-bed heat exchanger for flue gas heat recovery  

Science Conference Proceedings (OSTI)

In conventional flue gas heat recovery systems, the fouling by fly ashes and the related problems such as corrosion and cleaning are known to be major drawbacks. To overcome these problems, a single-riser no-distributor-fluidized-bed heat exchanger is devised and studied. Fouling and cleaning tests are performed for a uniquely designed fluidized bed-type heat exchanger to demonstrate the effect of particles on the fouling reduction and heat transfer enhancement. The tested heat exchanger model (1 m high and 54 mm internal diameter) is a gas-to-water type and composed of a main vertical tube and four auxiliary tubes through which particles circulate and transfer heat. Through the present study, the fouling on the heat transfer surface could successfully be simulated by controlling air-to-fuel ratios rather than introducing particles through an external feeder, which produced soft deposit layers with 1 to 1.5 mm thickness on the inside pipe wall. Flue gas temperature at the inlet of heat exchanger was maintained at 450{sup o}C at the gas volume rate of 0.738 to 0.768 CMM (0.0123 to 0.0128 m{sup 3}/sec). From the analyses of the measured data, heat transfer performances of the heat exchanger before and after fouling and with and without particles were evaluated. Results showed that soft deposits were easily removed by introducing glass bead particles, and also heat transfer performance increased two times by the particle circulation. In addition, it was found that this type of heat exchanger had high potential to recover heat of waste gases from furnaces, boilers, and incinerators effectively and to reduce fouling related problems.

Jun, Y.D.; Lee, K.B.; Islam, S.Z.; Ko, S.B. [Kongju National University, Kong Ju (Republic of Korea). Dept. for Mechanical Engineering

2008-07-01T23:59:59.000Z

304

Modeling and simulation of CO2 removal from power plant flue gas by PG solution in a hollow fiber membrane contactor  

Science Conference Proceedings (OSTI)

The absorption of carbon dioxide from nitrogen-carbon dioxide mixture was investigated in a polytetrafluoroethylene (PTFE) hollow fiber membrane module using potassium glycinate (PG) aqueous solution. A mathematical model was developed to simulate the ... Keywords: Absorption, Flue gas, Membrane contactor, Modeling, Potassium glycinate, Power plant

S. Eslami; S. M. Mousavi; S. Danesh; H. Banazadeh

2011-08-01T23:59:59.000Z

305

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

NLE Websites -- All DOE Office Websites (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

306

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

Science Conference Proceedings (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

307

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

DOE Green Energy (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

308

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

SciTech Connect

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

309

Development of a sorbent-based technology for control of mercury in flue gas  

Science Conference Proceedings (OSTI)

This paper presents results of research being, conducted at Argonne National Laboratory on the capture of elemental mercury in simulated flue gases by using dry sorbents. Experimental results from investigation of various sorbents and chemical additives for mercury control are reported. Of the sorbents investigated thus far, an activited-carbon-based sorbent impregnated with about 15% (by weight) of sulfur compound provided the best results. The key parameters affecting mercury control efficiency in a fixed-bed reactor, such as reactor loading, reactor temperature, sorbent size distribution, etc., were also studied, and the results ire presented. In addition to activated-carbon-based sorbents, a non-carbon-based sorbent that uses an inactive substrate treated with active chemicals is being developed. Preliminary, experimental results for mercury removal by this newly developed sorbent are presented.

Wu, Jiann M.; Huang, Hann S.; Livengood, C.D.

1996-03-01T23:59:59.000Z

310

Economical Desulfurization of Petroleum Coke  

Science Conference Proceedings (OSTI)

Presentation Title, Economical Desulfurization of Petroleum Coke ... " Desulfurization of Petroleum Coke Beyond 1600'C" by Christopher A. Paul of Great Lakes ...

311

Development of Superior Sorbents for Separation of CO2 from Flue Gas at a Wide Temperature range during Coal Combustion  

SciTech Connect

A number basic sorbents based on CaO were synthesized, characterized with novel techniques and tested for sorption of CO{sub 2} and selected gas mixtures simulating flue gas from coal fired boilers. Our studies resulted in highly promising sorbents which demonstrated zero affinity for N{sub 2}, O{sub 2}, SO{sub 2}, and NO very low affinity for water, ultrahigh CO{sub 2} sorption capacities, and rapid sorption characteristics, CO{sub 2} sorption at a very wide temperature range, durability, and low synthesis cost. One of the 'key' characteristics of the proposed materials is the fact that we can control very accurately their basicity (optimum number of basic sites of the appropriate strength) which allows for the selective chemisorption of CO{sub 2} at a wide range of temperatures. These unique characteristics of this family of sorbents offer high promise for development of advanced industrial sorbents for the effective CO{sub 2} removal.

Panagiotis Smirniotis

2002-09-17T23:59:59.000Z

312

Fundamental mechanisms in flue-gas conditioning. Topical report No. 1, Literature review and assembly of theories on the interactions of ash and FGD sorbents  

Science Conference Proceedings (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 ash 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.

Dahlin, R.S.; Vann Bush, P.; Snyder, T.R.

1992-01-09T23:59:59.000Z

313

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

Science Conference Proceedings (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

314

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

NLE Websites -- All DOE Office Websites (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-

315

Effects of HCl and SO{sub 2} concentration on mercury removal by activated carbon sorbents in coal-derived flue gas  

Science Conference Proceedings (OSTI)

The effect of the presence of HCl and SO{sub 2} in the simulated coal combustion flue gas on the Hg{sup 0} removal by a commercial activated carbon (coconut shell AC) was investigated in a laboratory-scale fixed-bed reactor in a temperature range of 80-200{sup o}C. The characteristics (thermal stability) of the mercury species formed on the sorbents under various adsorption conditions were investigated by the temperature-programmed decomposition desorption (TPDD) technique. It was found that the presence of HCl and SO{sub 2} in the flue gas affected the mercury removal efficiency of the sorbents as well as the characteristics of the mercury adsorption species. The mercury removal rate of AC increased with the HCl concentration in the flue gas. In the presence of HCl and the absence of SO{sub 2} during Hg{sup 0} adsorption by AC, a single Hg{sup 0} desorption peak at around 300{sup o}C was observed in the TPDD spectra and intensity of this peak increased with the HCl concentration during mercury adsorption. The peak at around 300{sup o}C may be derived from the decomposition and desorption of mercury chloride species. The presence of SO{sub 2} during mercury adsorption had an adverse effect on the mercury removal by AC in the presence of HCl. In the presence of both HCl and SO{sub 2} during Hg{sup 0} adsorption by AC, the major TPDD peak temperatures changed drastically depending upon the concentration of HCl and SO{sub 2} in flue gas during Hg{sup 0} adsorption. 16 refs., 7 figs.

Ryota Ochiai; M. Azhar Uddin; Eiji Sasaoka; Shengji Wu [Okayama University, Okayama (Japan). Faculty of Environmental Science and Technology

2009-09-15T23:59:59.000Z

316

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

E-Print Network (OSTI)

Shi, J.B. ; Feng, X.B. Mercury Pollution in China. Environ.J T. DOE/NETL’s Phase II Mercury Control Technology Fieldoxidants for the oxidation of mercury gas. Ind. vEng. Chem.

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

2008-01-01T23:59:59.000Z

317

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

SciTech Connect

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

318

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

SciTech Connect

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

319

DEVELOPMENT OF SUPERIOR SORBENTS FOR SEPARATION OF CO2 FROM FLUE GAS AT A WIDE TEMPERATURE RANGE DURING COAL COMBUSTION  

SciTech Connect

For this part of the project the studies focused on the development of novel sorbents for reducing the carbon dioxide emissions at high temperatures. Our studies focused on cesium doped CaO sorbents with respect to other major flue gas compounds in a wide temperature range. The thermo-gravimetric analysis of sorbents with loadings of CaO doped on 20 wt% cesium demonstrated high CO{sub 2} sorption uptakes (up to 66 wt% CO{sub 2}/sorbent). It is remarkable to note that zero adsorption affinity for N{sub 2}, O{sub 2}, H{sub 2}O and NO at temperatures as high as 600 C was observed. For water vapor and nitrogen oxide we observed a positive effect for CO{sub 2} adsorption. In the presence of steam, the CO{sub 2} adsorption increased to the highest adsorption capacity of 77 wt% CO{sub 2}/sorbent. In the presence of nitrogen oxide, the final CO{sub 2} uptake remained same, but the rate of adsorption was higher at the initial stages (10%) than the case where no nitrogen oxide was fed.

Panagiotis G. Smirniotis

2005-01-30T23:59:59.000Z

320

Use of flue gas desulphurisation (FGD) waste and rejected fly ash in waste stabilization/solidification systems  

Science Conference Proceedings (OSTI)

Stabilization/solidification (S/S) processes have been used as the final treatment step for hazardous wastes prior to land disposal. Fly ash is a by-product of coal-fired power generation; a significant proportion of this material is low-grade, reject material (rFA) that is unsuitable as a cement replacement due to its high carbon content and large particle size (>45 {mu}m). Flue gas desulphurization (FGD) sludge is a by-product from the air pollution control systems used in coal-fired power plants. The objective of this work was to investigate the performance of S/S waste binder systems containing these two waste materials (rFA and FGD). Strength tests show that cement-based waste forms with rFA and FGD replacement were suitable for disposal in landfills. The addition of an appropriate quantity of Ca(OH){sub 2} and FGD reduces the deleterious effect of heavy metals on strength development. Results of TCLP testing and the progressive TCLP test show that cement-rFA-Ca(OH){sub 2} systems with a range of FGD additions can form an effective S/S binder. The Leachability Index indicates that cement-based waste forms with rFA replacement were effective in reducing the mobility of heavy metals.

Qiao, X.C. [Department of Civil and Structural Engineering, Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (China); School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070 (China); Poon, C.S. [Department of Civil and Structural Engineering, Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (China)]. E-mail: cecspoon@polyu.edu.hk; Cheeseman, C. [Department of Civil and Environmental Engineering, Imperial College, London SW7 2BU (United Kingdom)

2006-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

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

322

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

323

Two-stage coal gasification and desulfurization  

DOE Patents (OSTI)

The present invention is directed to a system which effectively integrates a two-stage, fixed-bed coal gasification arrangement with hot fuel gas desulfurization of a first stream of fuel gas from a lower stage of the two-stage gasifier and the removal of sulfur from the sulfur sorbent regeneration gas utilized in the fuel-gas desulfurization process by burning a second stream of fuel gas from the upper stage of the gasifier in a combustion device in the presence of calcium-containing material. The second stream of fuel gas is taken from above the fixed bed in the coal gasifier and is laden with ammonia, tar and sulfur values. This second stream of fuel gas is burned in the presence of excess air to provide heat energy sufficient to effect a calcium-sulfur compound forming reaction between the calcium-containing material and sulfur values carried by the regeneration gas and the second stream of fuel gas. Any ammonia values present in the fuel gas are decomposed during the combustion of the fuel gas in the combustion chamber. The substantially sulfur-free products of combustion may then be combined with the desulfurized fuel gas for providing a combustible fluid utilized for driving a prime mover. 1 fig.

Bissett, L.A.; Strickland, L.D.

1990-08-03T23:59:59.000Z

324

LIFAC Sorbent Injection Desulfurization Demonstration Project. Quarterly report No. 13, October 1993--December 1993  

Science Conference Proceedings (OSTI)

In Dec 1989, the U.S. Department of Energy selected 13 projects for funding under the Federal Clean Coal Technology Program (Round III). One of the projects selected was the project sponsored by LIFAC North America, (LIFAC NA), titled {open_quotes}LIFAC Sorbent Injection Desulfurization Demonstration Project.{close_quotes} The host site for this $22 million, three-phase project is Richmond Power and Light`s Whitewater Valley Unit No. 2 in Richmond, Indiana. The LIFAC technology uses upper-furnace limestone injection with patented humidification of the flue gas to remove 75-85% of the sulfur dioxide (SO{sub 2}) in the flue gas. In November 1990, after a ten month negotiation period, LIFAC NA and the U.S. DOE entered into a Cooperative Agreement for the design, construction, and demonstration of the LIFAC system. This report is the thirteenth Technical Progress Report covering the period October 1, 1993 through the end of December 1993. Due to the power plant`s planned outage in March 1991, and the time needed for engineering, design and procurement of critical equipment, DOE and LIFAC NA agreed to execute the Design Phase of the project in Aug 1990, with DOE funding contingent upon final signing of the Cooperative Agreement.

Not Available

1994-05-01T23:59:59.000Z

325

Guidelines for Induced Flue Gas Recirculation: Volume 1: Reducing Air/Gas System Resistance and Enhancing Fan Capacity  

Science Conference Proceedings (OSTI)

This document guides users through a logical sequence, or "road map," of activities and decisions for optimizing solutions for fans, ducts, and related equipment in fossil plant combustion air and gas systems.

1999-12-13T23:59:59.000Z

326

High Volume--High Volume Usage of Flue Gas Desulfurization (FGD) By-Products in Underground Mines. Quarterly report, July 1-September 31, 1996  

SciTech Connect

The focus of activity for this quarter was the final selection and preparation of a mine site for the grout emplacement field demonstration. The site chosen is located in Floyd County, Kentucky and is owned by the Sunny Ridge Mining Company. Specifically, a northeast-trending highwall was selected that contains numerous auger holes of 31 inch diameter and varying depth. The coal has been deep- mined beyond the auger holes thus limiting their length. Access to the site is good, and the overlying strata are relatively un- weathered and competent. Preparation of the site involved culling a road to the highwall, followed by uncovering the auger holes which had previously been partially filled and graded with rock. The auger holes were then extensively characterized in the context of overall dimensions, condition, and extent of communication between holes. For this portion of the work, several types of apparatus were obtained, and constructed. Selection of a grout emplacement method was also completed. It was decided that concrete trucks will transport the dry FBC flyash to the site whereupon a specified amount of water will be added. This grout will then be transferred to a concrete pumping truck that will be used to inject the material into the auger holes. In this quarter, the arrangements necessary to complete the emplacement have been made.

NONE

1997-12-31T23:59:59.000Z

327

High-volume, high-value usage of Flue Gas Desulfurization (FGD) by-products in underground mines Phase 1: Laboratory investigations. Quarterly report, July 1994--September 1994  

SciTech Connect

During the quarter a second series of samples were collected and partially characterized chemically and mineralogically. The samples were collected at the disposal site operated by Freeman United Coal Co. The second collection was necessary because of deterioration due to hydration of the original samples. A study of the hydration characteristics was completed during the quarter. Important reactions included the immediate formation of ettringite and portlandite. The hydration and transformation was found to be a slow process. A second phase of gypsum formation from ettringite deterioration was identified. The slow hydration of anhydrite with its resultant swell is a potential problem which will be addressed further. Geotechnical characterization, during the quarter included completion of the preliminary characterization, analysis of the findings, experimentation with sample preparation for the final characterization/mix design, and design of the final experimental program. The analysis of the coals collected during the core drilling and hydrologic planning were completed. Also during the quarter a meeting was held with representatives of the shotcrete industry to discuss transport systems for emplacement. The pros and cons of pneumatic and hydraulic systems were discussed and plans formulated for further investigations.

NONE

1994-12-01T23:59:59.000Z

328

High-volume, high-value usage of flue gas desulfurization (FGD) by- products in underground mines: Phase 1, Laboratory investigations. Quarterly report, April--June 1995  

SciTech Connect

The kinetics study which is investigating hydration reactions of the ADM by-product (Subtask 2.2) was continued this quarter. This study further aided in gaining information on mineral precipitation and dissolution reactions during hydration of the ADM materials. The information is of importance for a comprehensive understanding of the factors that control strength and long-term stability during aging of FGD materials. The decision was made by Addington, Inc., DOE, and the University of Kentucky that the originally selected mine site for the emplacement demonstration must be changed, mainly for safety reasons. Mine selection will be a priority for the next quarter (Jul--Sep, 1995). Another activity during this reporting period was related to Subtask 4.3, the selection and testing of the transport system for the FGD material. A laboratory-scale pneumatic emplacement test unit (ETU) for dry FGD materials was built at the CAER to generate data so that a final selection of the field demonstration technology can be made. A dry pneumatic system was chosen for laboratory testing because the equipment and expertise available at the CAER matched this sort of technology best. While the design of the laboratory system was based on shotcrete technology, the physical properties of the emplaced FGD material is expected to be similar for other transport techniques, either pneumatic or hydraulic. In other words, the selection of a dry pneumatic transport system for laboratory testing does not necessarily imply that a scaled-up version will be used for the field demonstration. The ETU is a convenient means of producing samples for subsequent chemical and physical testing by a representative emplacement technology. Ultimately, the field demonstration technology will be chosen based on the laboratory data and the suitability of locally available equipment.

NONE

1995-09-01T23:59:59.000Z

329

Process for the elimination of waste water produced upon the desulfurization of coking oven gas by means of wash solution containing organic oxygen-carrier, with simultaneous recovery of elemental sulfur  

Science Conference Proceedings (OSTI)

A process is disclosed for the elimination of waste water falling out with the desulfurization of coking oven gas by means of an organic oxygen carrier-containing washing solution with simultaneous recovery of elemental sulfur. The waste water is decomposed in a combustion chamber in a reducing atmosphere at temperatures between about 1000/sup 0/ and 1100/sup 0/ C. under such conditions that the mole ratio of H/sub 2/S:SO/sub 2/ in the exhaust gas of the combustion chamber amounts to at least 2:1. Sulfur falling out is separated and the sensible heat of the exhaust gas is utilized for steam generation. The cooled and desulfurized exhaust gas is added to the coking oven gas before the pre-cooling. Sulfur falling out from the washing solution in the oxidizer is separated out and lead into the combustion chamber together with the part of the washing solution discharged as waste water from the washing solution circulation. Preferred embodiments include that the sulfur loading of the waste water can amount to up to about 370 kg sulfur per m/sup 3/ waste water; having the cooling of sulfur-containing exhaust gas leaving the combustion chamber follow in a waste heat boiler and a sulfur condenser heated by pre-heated boiler feed water, from which condenser sulfur is discharged in liquid state.

Diemer, P.; Brake, W.; Dittmer, R.

1985-04-16T23:59:59.000Z

330

COAL DESULFURIZATION PRIOR TO COMBUSTION  

E-Print Network (OSTI)

Corporation, 5-25~79. on Coal Liquefaction at ChevronHamersma, et a L, "Meyers Process for Coal Desulfurization,"in Wheelock, Coal Desulfurization, ACS Symp. Ser 64 (1977(.

Wrathall, J.

2013-01-01T23:59:59.000Z

331

The use of gypsum and a coal desulfurization by-product to ameliorate subsoil acidity for alfalfa growth  

E-Print Network (OSTI)

Acid soils limit the growth of aluminum-(Al) sensitive crops such as alfalfa (Medicago sativa L.). Management of acid subsoils can be difficult due to physical and economic constraints. Field experiments were conducted at two locations to evaluate the effectiveness of surface-applied gypsum and a flue gas desulfurization by-product for reducing the toxic effects of acid subsoils on alfalfa. The materials were applied at rates of 0, 5, 10, and 15 Mg ha-1. In addition, a glasshouse experiment was conducted that used 0, 5, and 10 Mg ha-1 of gypsum only. Field studies were concluded 41 and 45 months after treatment application at the two locations. No effect of material on alfalfa yield or tissue mineral concentration was observed. Also, rate did not affect yield. However, there were differences in plant tissue mineral concentration in several harvests that were related to rate. Soil was sampled periodically to 120 cm and indicated movement of Ca and S into the soil profile to depths of 60 and 120 cm, respectively. Subsoil pHH2O and pHCaCl2 were not affected by treatment. Extractable and exchangeable Al were not reduced by movement of Ca and S into the soil. In the glasshouse study, alfalfa yields and root growth were not affected by gypsum rate. As gypsum rate increased, plant tissue S increased, but K and Mg decreased. Alfalfa roots did not grow below 60 cm, even though there was indication of material movement to 90 cm in the soil. Although sulfur moved to 75 cm, no effect on soil Al was observed. Leachate collected from the bottoms of columns indicated that soil cations were leached as a result of gypsum application. Gypsum and the flue gas desulfurization by-product did not significantly affect the acid soils used in these studies or improve alfalfa growth.

Chessman, Dennis John

2003-12-01T23:59:59.000Z

332

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

Science Conference Proceedings (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

333

Flue heat reclaimer  

Science Conference Proceedings (OSTI)

A flue heat reclaimer is constructed to be mounted on the exterior of a flue duct of a heater and provide a spiral-shaped heat transfer passage extending around the flue duct. A fan causes air to flow through the heat transfer passage so that the temperature of this air is elevated by reason at its extended heat transfer relationship with the flue duct.

Paolino, R.J.

1983-05-03T23:59:59.000Z

334

DEVELOPMENT OF ANALYTICAL METHODS FOR THE QUANTIFICATION OF THE CHEMICAL FORMS OF MERCURY AND OTHER TARGET POLLUTANTS IN COAL-FIRED BOILER FLUE GAS  

Science Conference Proceedings (OSTI)

Since approximately 55% of the electrical power produced in the U. S. is generated by coal-based power utility plants, there is serious concern about the massive amounts of coal combustion products emitted into the atmosphere annually. Furthermore, Title III of the 1990 Clean Air Act Amendments (CAAA) requires the measurement and inventory of a possible 189 hazardous air pollutants (HAPs) from any stationary source producing more than 10 tons per year of any one pollutant or more than 25 tons per year of total pollutants. Although power utilities are not presently included on the list of source categories, the CAAA requires the U. S. Environmental Protection Agency to carry out a study of emissions from electricity generation using fossil fuels. Since many of these HAPs are known to be present in coal derived flue gas, coal-fired electric power utilities may be subject to regulation following these studies if Congress considers it necessary. In a cooperative effort with the U. S. Environmental Protection Agency (EPA), the U. S. Department of Energy (DOE) through its Federal Energy Technology Center (FETC) initiated such a study in 1991. DOE-FETC commissioned five primary contractors to conduct emission studies at eight different coal-fired electric utilities. The eight sites represented a cross section of feed coal type, boiler designs, and particulate and gaseous pollutant control technologies. The major goal of these studies was to determine the sampling and analytical methodologies that could be used efficiently to perform these emission tests while producing representative and reliable emission data. The successful methodology could then be recommended to the EPA for use in compliance testing in the event the regulation of air toxic emissions from coal-fired power plants is implemented. A secondary purpose of the testing was to determine the effectiveness of the control technologies in reducing target hazardous air pollutants. Advanced Technology Systems, Inc. (ATS) as a secondary DOE contractor on this project, assessed the sampling and analytical plans and the emission reports of the five primary contractors to determine how successful the contractors were in satisfying their defined objectives. ATS identified difficulties and inconsistencies in a number of sampling and analytical methodologies in these studies. In particular there was uncertainty as to the validity of the sampling and analytical methods used to differentiate the chemical forms of mercury observed in coal flue gas. Considering the differences in the mercury species with regard to human toxicity, the rate of transport through the ecosystem and the design variations in possible emission control schemes, DOE sought an accurate and reliable means to identify and quantify the various mercury compounds emitted by coal-fired utility boilers. ATS, as a contractor for DOE, completed both bench- and pilot-scale studies on various mercury speciation methods. The final validation of the modified Ontario-Hydro Method, its acceptance by DOE and submission of the method for adoption by ASTM was a direct result of these studies carried out in collaboration with the University of North Dakota's Energy and Environmental Research Center (UNDEERC). This report presents the results from studies carried out at ATS in the development of analytical methods to identify and quantify various chemical species, particularly those of mercury, in coal derived flue gas. Laboratory- and pilot-scale studies, not only on mercury species, but also on other inorganics and organics present in coal combustion flue gas are reported.

Terence J. McManus, Ph.D.

1999-06-30T23:59:59.000Z

335

Coal desulfurization with sodium hypochlorite.  

E-Print Network (OSTI)

??Wet desulfurization of Pittsburgh No. 8 coal and Illinois No. 6 coal were conducted with sodium hypochlorite in the laboratory. Pittsburgh No. 8 coal was… (more)

Li, Wei, M.S.

2004-01-01T23:59:59.000Z

336

Coal Liquefaction desulfurization process  

DOE Patents (OSTI)

In a solvent refined coal liquefaction process, more effective desulfurization of the high boiling point components is effected by first stripping the solvent-coal reacted slurry of lower boiling point components, particularly including hydrogen sulfide and low molecular weight sulfur compounds, and then reacting the slurry with a solid sulfur getter material, such as iron. The sulfur getter compound, with reacted sulfur included, is then removed with other solids in the slurry.

Givens, Edwin N. (Bethlehem, PA)

1983-01-01T23:59:59.000Z

337

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

Science Conference Proceedings (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

338

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

SciTech Connect

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

339

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

SciTech Connect

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 baghouse. Activated carbon was injected between the ESP and COHPAC units to collect the mercury. Short-term mercury removal levels in excess of 90% were achieved using the COHPAC 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. 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 system. The overall objective is to evaluate the long-term effects of sorbent injection on mercury capture and COHPAC 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

2003-10-31T23:59:59.000Z

340

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

Science Conference Proceedings (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

2004-08-06T23:59:59.000Z

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341

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

SciTech Connect

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

2004-10-25T23:59:59.000Z

342

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

SciTech Connect

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) baghouse to collect fly ash. The majority of the fly ash is collected in the ESP with the residual being collected in the COHPAC baghouse. Activated carbon was injected between the ESP and COHPAC units to collect the mercury. Short-term mercury removal levels in excess of 90% were achieved using the COHPAC 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. 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 system. The overall objective is to evaluate the long-term effects of sorbent injection on mercury capture and COHPAC 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) approach.

Jean Bustard; Charles Lindsey; Paul Brignac; Travis Starns; Sharon Sjostrom; Tom Millar

2003-07-30T23:59:59.000Z

343

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

Science Conference Proceedings (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; Cindy Larson

2006-01-27T23:59:59.000Z

344

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

Science Conference Proceedings (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; Cindy Larson

2006-04-24T23:59:59.000Z

345

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

Science Conference Proceedings (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; Cindy Larson

2005-10-24T23:59:59.000Z

346

LIFAC Sorbent Injection Desulfurization Demonstration Project. Quarterly report No. 12, July--September 1993  

Science Conference Proceedings (OSTI)

In December 1989, the U.S. Department of Energy selected 13 projects for funding under the Federal Clean Coal Technology Program (Round III). One of the projects selected was the project sponsored by LIFAC North America, (LIFAC NA), titled {open_quotes}LIFAC Sorbent Injection Desulfurization Demonstration Project.{close_quotes} The LIFAC technology uses upper-furnace limestone injection with patented humidification of the flue gas to remove 75-85% of the sulfur dioxide (SO{sub 2}) in the flue gas. The host site for this $22 million, three-phase project is Richmond Power and Light`s Whitewater Valley Unit No. 2 in Richmond, Indiana. The three project phases are: (1) Design; (2A) Long Lead Procurement; (2B) Construction; and (3) Operations. The design phase began on August 8, 1990 and was scheduled to last six months. Phase 2A, long lead procurement, overlaps the design phase and was expected to require about four months to complete. The construction phase was then to continue for another seven months, while the operations phase was scheduled to last about twenty-six months. In November 1990, after a ten (10) month negotiation period, LIFAC NA and the U.S. DOE entered into a Cooperative Agreement for the design, construction, and demonstration of the LIFAC system. This report is the twelfth Technical Progress Report covering the period July 1, 1993 through the end of September 1993. Due to the power plant`s planned outage in March 1991, and the time needed for engineering, design and procurement of critical equipment, DOE and LIFAC NA agreed to execute the Design Phase of the project in August 1990, with DOE funding contingent upon final signing of the Cooperative Agreement.

Not Available

1993-12-31T23:59:59.000Z

347

Puerto Rico Refinery Desulfurization, Gasoline Downstream Charge ...  

U.S. Energy Information Administration (EIA)

Puerto Rico Refinery Desulfurization, Gasoline Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

348

Method for desulfurization of coal  

DOE Patents (OSTI)

A process and apparatus are disclosed for desulfurizing coal which removes sulfur in the inorganic and organic form by preferentially heating the inorganic iron sulfides in coal in a flowing gas to convert some of the inorganic iron sulfides from a pyrite form FeS[sub 2] to a troilite FeS form or a pyrrhotite form Fe[sub 1[minus]x]S and release some of the sulfur as a gaseous compound. The troilite and pyrrhotite forms are convenient catalyst for removing the organic sulfur in the next step, which is to react the coal with chemical agents such as alcohol, thus removing the organic sulfur as a liquid or a gas such as H[sub 2]S. The remaining inorganic sulfur is left in the predominantly higher magnetic form of pyrrhotite and is then removed by magnetic separation techniques. Optionally, an organic flocculant may be added after the organic sulfur has been removed and before magnetic separation. The flocculant attaches non-pyrite minerals with the pyrrhotite for removal by magnetic separation to reduce the ash-forming contents. 2 figs.

Kelland, D.R.

1987-07-07T23:59:59.000Z

349

Two-stage coal gasification and desulfurization apparatus  

DOE Patents (OSTI)

The present invention is directed to a system which effectively integrates a two-stage, fixed-bed coal gasification arrangement with hot fuel gas desulfurization of a first stream of fuel gas from a lower stage of the two-stage gasifier and the removal of sulfur from the sulfur sorbent regeneration gas utilized in the fuel-gas desulfurization process by burning a second stream of fuel gas from the upper stage of the gasifier in a combustion device in the presence of calcium-containing material. The second stream of fuel gas is taken from above the fixed bed in the coal gasifier and is laden with ammonia, tar and sulfur values. This second stream of fuel gas is burned in the presence of excess air to provide heat energy sufficient to effect a calcium-sulfur compound forming reaction between the calcium-containing material and sulfur values carried by the regeneration gas and the second stream of fuel gas. Any ammonia values present in the fuel gas are decomposed during the combustion of the fuel gas in the combustion chamber. The substantially sulfur-free products of combustion may then be combined with the desulfurized fuel gas for providing a combustible fluid utilized for driving a prime mover.

Bissett, Larry A. (Morgantown, WV); Strickland, Larry D. (Morgantown, WV)

1991-01-01T23:59:59.000Z

350

Enhanced durability and reactivity for zinc ferrite desulfurization sorbent  

Science Conference Proceedings (OSTI)

AMAX Research Development Center (AMAX R D) has been investigating methods for enhancing the reactivity and durability of the zinc ferrite desulfurization sorbent. Zinc ferrite sorbents are intended for use in desulfurization of hot coal gas in integrated gasification combined cycle (IGCC) or molten carbonate fuel cell (MCFC) applications. For the present program, the reactivity of the sorbent may be defined as its sulfur sorption capacity at the breakthrough point and at saturation in a bench-scale, fixed-bed reactor. Durability may be defined as the ability of the sorbent to maintain important physical characteristics such As size, strength, and specific surface area during 10 cycles of sulfidation and oxidation.

Jha, M.C.; Berggren, M.H.

1989-05-02T23:59:59.000Z

351

The Biocatalytic Desulfurization Project  

DOE Green Energy (OSTI)

The material in this report summarizes the Diversa technical effort in development of a biocatalyst for the biodesulfurization of Petro Star diesel as well as an economic report of standalone and combined desulfurization options, prepared by Pelorus and Anvil, to support and inform the development of a commercially viable process. We will discuss goals of the projected as originally stated and their modification as guided by parallel efforts to evaluate commercialization economics and process parameters. We describe efforts to identify novel genes and hosts for the generation of an optimal biocatalyst, analysis of diesel fuels (untreated, chemically oxidized and hydrotreated) for organosulfur compound composition and directed evolution of enzymes central to the biodesulfurization pathway to optimize properties important for their use in a biocatalyst. Finally we will summarize the challenges and issues that are central to successful development of a viable biodesulfurization process.

David Nunn; James Boltz; Philip M. DiGrazia; Larry Nace

2006-03-03T23:59:59.000Z

352

A NOVEL APPROACH TO CATALYTIC DESULFURIZATION OF COAL  

DOE Green Energy (OSTI)

Column chromatographic separation of the S=PBu{sub 3}/PBu{sub 3} product mixture followed by weighing the S=PBu{sub 3}, and by vacuum distillation of S=PBu{sub 3}/PBu{sub 3}mixture followed by gas chromatographic analysis are described. Effects of coal mesh size, pre-treatment with methanol Coal (S) + excess PR{sub 3} {yields} Coal + S=PR{sub 3}/PBu{sub 3} and sonication on sulfur removal by PBu{sub 3} revealed that particle size was not observed to affect desulfurization efficiency in a consistent manner. Coal pretreatment with methanol to induce swelling or the addition of a filter aid such as Celite reduced desulfurization efficiency of the PBu{sub 3} and sonication was no more effective than heating. A rationale is put forth for the lack of efficacy of methanol pretreatment of the coal in desulfurization runs with PBu{sub 3}. Coal desulfurization with PBu{sub 3} was not improved in the presence of miniscule beads of molten lithium or sodium as a desulfurizing reagent for SPBu{sub 3} in a strategy aimed at regenerating PBu{sub 3} inside coal pores. Although desulfurization of coals did occur in sodium solutions in liquid ammonia, substantial loss of coal mass was also observed. Of particular concern is the mass balance in the above reaction, a problem which is described in some detail. In an effort to solve this difficulty, a specially designed apparatus is described which we believe can solve this problem reasonably effectively. Elemental sodium was found to remove sulfur quantitatively from a variety of polycyclic organosulfur compounds including dibenzothiophene and benzothiophene under relatively mild conditions (150 C) in a hydrocarbon solvent without requiring the addition of a hydrogen donor. Lithium facilitates the same reaction at a higher temperature (254 C). Mechanistic pathways are proposed for these transformations. Curiously, dibenzothiophene and its corresponding sulfone was virtually quantitatively desulfurized in sodium solutions in liquid ammonia at -33 C, although the yield of biphenyl was only about 20 to 30%. On the other hand, benzothiophene gave a high yield of 2-ethylthiophenol under these conditions. Although our superbase P(MeNCH{sub 2}CH{sub 2}){sub 3}N, which is now commercially available, is a more effective desulfurizing agent for a variety of organophosphorus compounds than PPh{sub 3} or its acyclic analogue P(NMe){sub 3}, it does not desulfurize benzothiophene or dibenzothiophene.

John G. Verkade

2001-11-01T23:59:59.000Z

353

Application Investigation on Polyureas Anticorrosion for Concrete Surface in Desulphurization Flue  

Science Conference Proceedings (OSTI)

Application investigation on polyureas anticorrosion in flue of Wet Flue Gas Desulphurization Equipment (FGD) (product model: DTTW-? -150) was carried out according to corrosive environment and technical parameters of a coal-fired power plan. And ... Keywords: spray, polyureas, flue, corrosion margin

Song Wei; Liu Zongyu

2010-03-01T23:59:59.000Z

354

Development of new sorbents to remove mercury and selenium from flue gas. Final report, September 1, 1993--August 31, 1994  

Science Conference Proceedings (OSTI)

Mercury (Hg) and selenium (Se) are two of the volatile trace metals in coal, which are often not captured by conventional gas clean up devices of coal-fired boilers. An alternative is to use sorbents to capture the volatile components of trace metals after coal combustion. In this project sorbent screening tests were performed in which ten sorbents were selected to remove metallic mercury in N{sub 2}. These sorbents included activated carbon, char prepared from Ohio No. 5 coal, molecular sieves, silica gel, aluminum oxide, hydrated lime, Wyoming bentonite, kaolin, and Amberite IR-120 (an ion-exchanger). The sorbents were selected based on published information and B&W`s experience on mercury removal. The promising sorbent was then selected and modified for detailed studies of removal of mercury and selenium compounds. The sorbents were tested in a bench-scale adsorption facility. A known amount of each sorbent was loaded in the column as a packed bed. A carrier gas was bubbled through the mercury and selenium compounds. The vaporized species were carried by the gas and went through the sorbent beds. The amount of mercury and selenium compounds captured by the sorbents was determined by atomic absorption. Results are discussed.

Shiao, S.Y. [Babcock and Wilcox Co., Alliance, OH (United States)

1995-02-01T23:59:59.000Z

355

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

Science Conference Proceedings (OSTI)

This document provides a summary of the full-scale demonstration efforts involved in the project ''Field Test Program for Long-Term Operation of a COHPAC{reg_sign} System for Removing Mercury from Coal-Fired Flue Gas''. The project took place at Alabama Power's Plant Gaston Unit 3 and involved the injection of sorbent between an existing particulate collector (hot-side electrostatic precipitators) and a COHPAC{reg_sign} fabric filter (baghouse) downstream. Although the COHPAC{reg_sign} baghouse was designed originally for polishing the flue gas, when activated carbon injection was added, the test was actually evaluating the EPRI TOXECON{reg_sign} configuration. The results from the baseline tests with no carbon injection showed that the cleaning frequency in the COHPAC{reg_sign} unit was much higher than expected, and was above the target maximum cleaning frequency of 1.5 pulses/bag/hour (p/b/h), which was used during the Phase I test in 2001. There were times when the baghouse was cleaning continuously at 4.4 p/b/h. In the 2001 tests, there was virtually no mercury removal at baseline conditions. In this second round of tests, mercury removal varied between 0 and 90%, and was dependent on inlet mass loading. There was a much higher amount of ash exiting the electrostatic precipitators (ESP), creating an inlet loading greater than the design conditions for the COHPAC{reg_sign} baghouse. Tests were performed to try to determine the cause of the high ash loading. The LOI of the ash in the 2001 baseline tests was 11%, while the second baseline tests showed an LOI of 17.4%. The LOI is an indication of the carbon content in the ash, which can affect the native mercury uptake, and can also adversely affect the performance of ESPs, allowing more ash particles to escape the unit. To overcome this, an injection scheme was implemented that balanced the need to decrease carbon injection during times when inlet loading to the baghouse was high and increase carbon injection when inlet loading and mercury removal were low. The resulting mercury removal varied between 50 and 98%, with an overall average of 85.6%, showing that the process was successful at removing high percentages of vapor-phase mercury even with a widely varying mass loading. In an effort to improve baghouse performance, high-permeability bags were tested. The new bags made a significant difference in the cleaning frequency of the baghouse. Before changing the bags, the baghouse was often in a continuous clean of 4.4 p/b/h, but with the new bags the cleaning frequency was very low, at less than 1 p/b/h. Alternative sorbent tests were also performed using these high-permeability bags. The results of these tests showed that most standard, high-quality activated carbon performed similarly at this site; low-cost sorbent and ash-based sorbents were not very effective at removing mercury; and chemically enhanced sorbents did not appear to offer any benefits over standard activated carbons at this site.

C. Jean Bustard; Charles Lindsey; Paul Brignac

2006-05-01T23:59:59.000Z

356

THE BIOCATALYTIC DESULFURIZATION PROJECT  

DOE Green Energy (OSTI)

The analysis of Petro Star diesel sulfur species is complete and a report is attached. Further analytical efforts will concentrate on characterization of diesel fuel, hydrodesulfurized to varying degrees, in order to determine sulfur species that may be problematic to hydrogen treatment and represent potential target substrates for biodesulfurization in a combined HDS-BDS process. Quotes have been received and are being considered for the partial treatment of Petro Star Inc. marine diesel fuel. Direction of research is changing slightly; economic analysis of the hyphenated--BDSHDS, BDS-CED--has shown the highest probability of success to be with a BDS-HDS process where the biodesulfurization precedes hydrodesulfurization. Thus, the microorganisms will be tailored to focus on those compounds that tend to be recalcitrant to hydrodesulfurization and decrease the severity of the hydrodesulfurization step. A separate, detailed justification for this change is being prepared. Research activities have continued in the characterization of the desulfurization enzymes from multiple sources. Genes for all DszA, -B, -C and -D enzymes (and homologs) have been cloned and expressed. Activity determinations, on a variety of substituted benzothiophene and dibenzothiophene substrates, have been carried out and continue. In addition, chemical synthesis efforts have been carried out to generate additional substrates for analytical standards and activity determinations. The generation of a GSSM mutant library of the ''Rhodococcus IGTS8 dszA'' gene has been completed and development of protocols for a high throughput screen to expand substrate specificity are nearing completion. In an effort to obtain improved hosts as biocatalyst, one hundred-thirty ''Rhodococcus'' and related strains are being evaluated for growth characteristics and other criteria deemed important for an optimal biocatalyst strain. We have also begun an effort to generate derivatives of the entire IGTS8 BDS plasmid that will allow for its easy transfer and manipulation into a variety of hosts. To support this activity and to gain an understanding of additional genes that may potentially affect BDS activity, the nucleotide sequence of the entire complement of plasmids in IGTS8 is being determined. Lastly, we continue to develop genetic screens and selections for the discovery and improvement of the biodesulfurization genes and strains.

Scott Collins; David Nunn

2003-10-01T23:59:59.000Z

357

Desulfurization sorbent regeneration  

DOE Patents (OSTI)

A spent solid sorbent resulting from the removal of hydrogen sulfide from a fuel gas flow is regenerated with a steam-air mixture. The mixture of steam and air may also include additional nitrogen or carbon dioxide. The gas mixture contacts the spent sorbent containing metal sulfide at a temperature above 500/sup 0/C to regenerate the sulfide to metal oxide or carbonate. Various metal species including the period four transition metals and the lanthanides are suitable sorbents that may be regenerated by this method. In addition, the introduction of carbon dioxide gas permits carbonates such as those of strontium, barium and calcium to be regenerated. The steam permits regeneration of spent sorbent without formation of metal sulfate. Moreover, the regeneration will proceed with low oxygen concentrations and will occur without the increase in temperature to minimize the risk of sintering and densification of the sorbent. This method may be used for high-temperature fuel cells.

Jalan, V.M.; Frost, D.G.

1982-07-07T23:59:59.000Z

358

Toxic emissions from a cyclone burner boiler with an ESP and with the SNOX demonstration and from a pulverized coal burner boiler with an ESP/wet flue gas desulfurization system  

SciTech Connect

Emission factors for VOC and aldehydes, dioxins/furans, and PAH/SVOC are presented in Tables 6--8, respectively. Each table includes results for Coal Creek, Niles Boiler, and the SNOX process. As shown in Table 6, benzene and toluene were measured in the Coal Creek, Niles Boiler, and SNOX stack emissions in highly variable concentrations. Over 90 percent of the VOC analyzed were not detected in the stack gases, and the emission factor for these VOC ranges from 1.1 to 1.4 {mu}g/MJ for the three systems. Emission factors for the four aldehydes that were measured range from 0.47 to 31 {mu}g/MJ for Coal Creek, 1.7 to 38 {mu}g/MJ for the Niles Boiler, and 3.6 to 167 {mu}g/MJ for the SNOX process. Acetaldehyde is at the highest concentration of the four aldehydes in all three units, a finding which is consistent with previous work. Dioxin/furan emission factors are provided in Table 7. Emission, factors for these compounds range from 0.40 to 6.51 pg/MJ for Coal Creek and 0.45 to 8.14 pg/MJ for the Niles Boiler. Dioxins/furans were not determined in the SNOX process. The compounds 1,2,3,4,6,7,8heptachlorodibenzo-p-dioxin, octachlorodibenzo-p-dioxin, and 2,3,7,8-tetrachlorodibenzofuran were detected in both units. The predominance of these species in high SO{sub 2} environments has been previously observed. All other 2,3,7,8 substituted dioxin/furan isomers listed in Table 8 were not detected in either unit. Table 8 lists the emission factors for PAH/SVOC. Emission factors range from 0.3 to 233 ng/MJ for Coal Creek, 0.5 to 273 ng/MJ for the Niles Boiler, and 0.3 to 130 ng/MJ for the SNOX process. Acetophenone is at the highest concentration of the PAH/SVOC in all three units. Naphthalene, dibenzofuran, phenanthrene, and fluoranthene are also present at relatively high concentrations in comparison to the other PAH/SVOC.

Sverdrup, G.M.; Riggs, K.B.; Kelly, T.J.; Barrett, R.E. [Battelle, Columbus, OH (United States); Peltier, R.G.; Cooper, J.A. [Chester Environmental, Monroeville, PA (United States)

1994-05-01T23:59:59.000Z

359

Low temperature aqueous desulfurization of coal  

DOE Patents (OSTI)

This invention describes a chemical process for desulfurizing coal, especially adaptable to the treatment of coal-water slurries, at temperatures as low as ambient, comprising treating the coal with aqueous titanous chloride whereby hydrogen sulfide is liberated and the desulfurized coal is separated with the conversion of titanous chloride to titanium oxides.

Slegeir, William A. (Hampton Bays, NY); Healy, Francis E. (Massapequa, NY); Sapienza, Richard S. (Shoreham, NY)

1985-01-01T23:59:59.000Z

360

Low temperature aqueous desulfurization of coal  

DOE Patents (OSTI)

This invention describes a chemical process for desulfurizing coal, especially adaptable to the treatment of coal-water slurries, at temperatures as low as ambient, comprising treating the coal with aqueous titanous chloride whereby hydrogen sulfide is liberated and the desulfurized coal is separated with the conversion of titanous chloride to titanium oxides.

Slegeir, W.A.; Healy, F.E.; Sapienza, R.S.

1985-04-18T23:59:59.000Z

Note: This page contains sample records for the topic "flue gas desulfurization" 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

DEEP DESULFURIZATION OF DIESEL FUELS BY A NOVEL INTEGRATED APPROACH  

DOE Green Energy (OSTI)

The overall objective of this project is to explore a new desulfurization system concept, which consists of efficient separation of the refractory sulfur compounds from diesel fuel by selective adsorption, and effective hydrodesulfurization of the concentrated fraction of the refractory sulfur compounds in diesel fuels. Our approaches focused on (1) selecting and developing new adsorbents for selective adsorption of sulfur or sulfur compounds in commercial diesel fuel; (2) conducting the adsorption desulfurization of model fuels and real diesel fuels by the selective-adsorption-for-removing-sulfur (PSUSARS) process over various developed adsorbents, and examining the adsorptive desulfurization performance of various adsorbents; (3) developing and evaluating the regeneration methods for various spent adsorbent; (4) developing new catalysts for hydrodesulfurization of the refractory sulfur existing in the commercial diesel fuel; (5) on the basis of the fundamental understanding of the adsorptive performance and regeneration natures of the adsorbents, further confirming and improving the conceptual design of the novel PSU-SARS process for deep desulfurization of diesel fuel Three types of adsorbents, the metal-chloride-based adsorbents, the activated nickel-based adsorbents and the metal-sulfide-based adsorbents, have been developed for selective adsorption desulfurization of liquid hydrocarbons. All of three types of the adsorbents exhibit the significant selectivity for sulfur compounds, including alkyl dibenzothiophenes (DBTs), in diesel fuel. Adsorption desulfurization of real diesel fuels (regular diesel fuel (DF), S: 325 ppmw; low sulfur diesel fuel (LSD-I), S: 47 ppmw) over the nickel-based adsorbents (A-2 and A-5) has been conducted at different conditions by using a flowing system. The adsorption capacity of DF over A-2 corresponding to an outlet sulfur level of 30 ppmw is 2.8 mg-S/g-A. The adsorption capacity of LSD-I over A-5 corresponding to the break-through point at 5.0 ppmw sulfur level is 0.35 mg-S/g-A. The spent A-5 can be regenerated by using H2 gas at a flowing rate of 40-50 ml/min, 500 C, and ambient pressure. Adsorption desulfurization of model diesel fuels over metal-sulfide-based adsorbents (A-6-1 and A-6-2) has been conducted at different temperatures to examine the capacity and selectivity of the adsorbents. A regeneration method for the spent metal-sulfide-based adsorbents has been developed. The spent A-6-1 can be easily regenerated by washing the spent adsorbent with a polar solvent followed by heating the adsorbent bed to remove the remainder solvent. Almost all adsorption capacity of the fresh A-6-1 can be recovered after the regeneration. On the other hand, a MCM-41-supported HDS catalyst was developed for deep desulfurization of the refractory sulfur compounds. The results show that the developed MCM-41-supported catalyst demonstrates consistently higher activity for the HDS of the refractory dibenzothiophenic sulfur compounds than the commercial catalyst. On the basis of the fundamental understanding of the adsorptive performance and regeneration natures of the adsorbents, the conceptual design of the novel PSU-SARS process for deep desulfurization of diesel fuel is confirmed and improved further.

Xiaoliang Ma; Uday Turaga; Shingo Watanabe; Subramani Velu; Chunshan Song

2004-05-01T23:59:59.000Z

362

CONVERSION EXTRACTION DESULFURIZATION (CED) PHASE III  

DOE Green Energy (OSTI)

This project was undertaken to refine the Conversion Extraction Desulfurization (CED) technology to efficiently and economically remove sulfur from diesel fuel to levels below 15-ppm. CED is considered a generic term covering all desulfurization processes that involve oxidation and extraction. The CED process first extracts a fraction of the sulfur from the diesel, then selectively oxidizes the remaining sulfur compounds, and finally extracts these oxidized materials. The Department of Energy (DOE) awarded Petro Star Inc. a contract to fund Phase III of the CED process development. Phase III consisted of testing a continuous-flow process, optimization of the process steps, design of a pilot plant, and completion of a market study for licensing the process. Petro Star and the Degussa Corporation in coordination with Koch Modular Process Systems (KMPS) tested six key process steps in a 7.6-centimeter (cm) (3.0-inch) inside diameter (ID) column at gas oil feed rates of 7.8 to 93.3 liters per hour (l/h) (2.1 to 24.6 gallons per hour). The team verified the technical feasibility with respect to hydraulics for each unit operation tested and successfully demonstrated pre-extraction and solvent recovery distillation. Test operations conducted at KMPS demonstrated that the oxidation reaction converted a maximum of 97% of the thiophenes. The CED Process Development Team demonstrated that CED technology is capable of reducing the sulfur content of light atmospheric gas oil from 5,000-ppm to less than 15-ppm within the laboratory scale. In continuous flow trials, the CED process consistently produced fuel with approximately 20-ppm of sulfur. The process economics study calculated an estimated process cost of $5.70 per product barrel. The Kline Company performed a marketing study to evaluate the possibility of licensing the CED technology. Kline concluded that only 13 refineries harbored opportunity for the CED process. The Kline study and the research team's discussions with prospective refineries led to the conclusion that there were not likely prospects for the licensing of the CED process.

James Boltz

2005-03-01T23:59:59.000Z

363

Methods, systems, and devices for deep desulfurization of fuel gases  

DOE Patents (OSTI)

A highly effective and regenerable method, system and device that enables the desulfurization of warm fuel gases by passing these warm gasses over metal-based sorbents arranged in a mesoporous substrate. This technology will protect Fischer-Tropsch synthesis catalysts and other sulfur sensitive catalysts, without drastic cooling of the fuel gases. This invention can be utilized in a process either alone or alongside other separation processes, and allows the total sulfur in such a gas to be reduced to less than 500 ppb and in some instances as low as 50 ppb.

Li, Liyu (Richland, WA); King, David L. (Richland, WA); Liu, Jun (Richland, WA); Huo, Qisheng (Richland, WA)

2012-04-17T23:59:59.000Z

364

Assessment of coal gasification/hot gas cleanup based advanced gas turbine systems  

SciTech Connect

The major objectives of the joint SCS/DOE study of air-blown gasification power plants with hot gas cleanup are to: (1) Evaluate various power plant configurations to determine if an air-blown gasification-based power plant with hot gas cleanup can compete against pulverized coal with flue gas desulfurization for baseload expansion at Georgia Power Company's Plant Wansley; (2) determine if air-blown gasification with hot gas cleanup is more cost effective than oxygen-blown IGCC with cold gas cleanup; (3) perform Second-Law/Thermoeconomic Analysis of air-blown IGCC with hot gas cleanup and oxygen-blown IGCC with cold gas cleanup; (4) compare cost, performance, and reliability of IGCC based on industrial gas turbines and ISTIG power island configurations based on aeroderivative gas turbines; (5) compare cost, performance, and reliability of large (400 MW) and small (100 to 200 MW) gasification power plants; and (6) compare cost, performance, and reliability of air-blown gasification power plants using fluidized-bed gasifiers to air-blown IGCC using transport gasification and pressurized combustion.

1990-12-01T23:59:59.000Z

365

Desulfurization with transition metal catalysts. Quarterly summary  

SciTech Connect

The overall objective of this research is to develop desulfurizing transition metal catalysts, which are active in homogeneous media at moderate temperatures and pressures for the purification of coal-derived fuels and chemicals. To this end, the mechanism of action is being examined whereby newly identified nickel(0) complexes desulfurize organosulfur compounds in solution at 65 to 70/sup 0/C. The sulfur compounds under investigation are typical of those commonly encountered in coal-derived liquids and solids, such as thiophenes, sulfides and mercaptans. The following studies on the homogeneous, stoichiometric desulfurizing agent, bis(1,5-cyclooctadiene) nickel(0) ((COD)/sub 2/Ni), were continued: (a) activation of the agent by means of added mono-, bi-/sup 2/ and tri-dentate amines, either of the tertiary or primary amine type; (b) labeling studies designed to reveal the source of the hydrogen that replaces the sulfur in the desulfurization of dibenzothiophene; (c) comparison of the desulfurizing activity of (COD)/sub 2/Ni, both in the presence and in the absence of lithium aluminum hydride; and (d) testing for the role of any biphenylene intermediate in these desulfurizations. Results are reported.

Eisch, J J

1980-04-10T23:59:59.000Z

366

Pressurized fluidized-bed hydroretorting of Eastern oil shales -- Sulfur control. Topical report for Subtask 3.1, In-bed sulfur capture tests; Subtask 3.2, Electrostatic desulfurization; Subtask 3.3, Microbial desulfurization and denitrification  

SciTech Connect

This topical report on ``Sulfur Control`` presents the results of work conducted by the Institute of Gas Technology (IGT), the Illinois Institute of Technology (IIT), and the Ohio State University (OSU) to develop three novel approaches for desulfurization that have shown good potential with coal and could be cost-effective for oil shales. These are (1) In-Bed Sulfur Capture using different sorbents (IGT), (2) Electrostatic Desulfurization (IIT), and (3) Microbial Desulfurization and Denitrification (OSU and IGT). The objective of the task on In-Bed Sulfur Capture was to determine the effectiveness of different sorbents (that is, limestone, calcined limestone, dolomite, and siderite) for capturing sulfur (as H{sub 2}S) in the reactor during hydroretorting. The objective of the task on Electrostatic Desulfurization was to determine the operating conditions necessary to achieve a high degree of sulfur removal and kerogen recovery in IIT`s electrostatic separator. The objectives of the task on Microbial Desulfurization and Denitrification were to (1) isolate microbial cultures and evaluate their ability to desulfurize and denitrify shale, (2) conduct laboratory-scale batch and continuous tests to improve and enhance microbial removal of these components, and (3) determine the effects of processing parameters, such as shale slurry concentration, solids settling characteristics, agitation rate, and pH on the process.

Roberts, M.J.; Abbasian, J.; Akin, C.; Lau, F.S.; Maka, A.; Mensinger, M.C.; Punwani, D.V.; Rue, D.M. [Institute of Gas Technology, Chicago, IL (United States); Gidaspow, D.; Gupta, R.; Wasan, D.T. [Illinois Inst. of Tech., Chicago, IL (United States); Pfister, R.M.: Krieger, E.J. [Ohio State Univ., Columbus, OH (United States)

1992-05-01T23:59:59.000Z

367

A BP neural network predictor model for desulfurizing molten iron  

Science Conference Proceedings (OSTI)

Desulfurization of molten iron is one of the stages of steel production process. A back-propagation (BP) artificial neural network (ANN) model is developed to predict the operation parameters for desulfurization process in this paper. The primary objective ...

Zhijun Rong; Binbin Dan; Jiangang Yi

2005-07-01T23:59:59.000Z

368

Control of pollutants in flue gases and fuel gases  

E-Print Network (OSTI)

. Mercury typically forms the sulfide (HgS) #12;4 because of the prevalence of sulfides in volcanic gases Aq + 2e-- ´ Hg0 Atmos Equation 1 Ionic mercury can form from the oxidation of elemental mercury Coal is known to contain mercury as a result of testing done upon the flue gas emitted from power plant

Laughlin, Robert B.

369

Word Pro - Untitled1  

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

1985-2010 (Megawatts) Year Coal Petroleum and Natural Gas Total 1 Particulate Collectors Cooling Towers Flue Gas Desulfurization (Scrubbers) Total 2 Particulate Collectors Cooling...

370

Thermophilic Methanol Utilization by  

E-Print Network (OSTI)

: acetate ADH: alcohol dehydrogenase Bio-FGD: biological flue-gas desulfurization COD: chemical oxygen desulfurization In sub-section 1.1.1, sulfur dioxide emission and general aspects of the flue gas desulfurization heaters, metallurgical operations, roasting and sintering, coke oven plants, processing of titanium

Groningen, Rijksuniversiteit

371

Table 11.6 Installed Nameplate Capacity of Fossil-Fuel Steam-Electric Generators With Environmental Equipment, 1985-2010 (Megawatts)  

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

Installed Nameplate Capacity of Fossil-Fuel Steam-Electric Generators With Environmental Equipment," Installed Nameplate Capacity of Fossil-Fuel Steam-Electric Generators With Environmental Equipment," " 1985-2010 (Megawatts)" "Year","Coal",,,,"Petroleum and Natural Gas",,,,"Total 1" ,,,"Flue Gas","Total 2",,,"Flue Gas","Total 2",,,"Flue Gas","Total 2" ,"Particulate","Cooling","Desulfurization",,"Particulate","Cooling","Desulfurization",,"Particulate","Cooling","Desulfurization" ,"Collectors","Towers","(Scrubbers)",,"Collectors","Towers","(Scrubbers)",,"Collectors","Towers","(Scrubbers)"

372

Evaluation of gasification and gas cleanup processes for use in molten carbonate fuel cell power plants. Final report. [Contains lists and evaluations of coal gasification and fuel gas desulfurization processes  

DOE Green Energy (OSTI)

This report satisfies the requirements for DOE Contract AC21-81MC16220 to: List coal gasifiers and gas cleanup systems suitable for supplying fuel to molten carbonate fuel cells (MCFC) in industrial and utility power plants; extensively characterize those coal gas cleanup systems rejected by DOE's MCFC contractors for their power plant systems by virtue of the resources required for those systems to be commercially developed; develop an analytical model to predict MCFC tolerance for particulates on the anode (fuel gas) side of the MCFC; develop an analytical model to predict MCFC anode side tolerance for chemical species, including sulfides, halogens, and trace heavy metals; choose from the candidate gasifier/cleanup systems those most suitable for MCFC-based power plants; choose a reference wet cleanup system; provide parametric analyses of the coal gasifiers and gas cleanup systems when integrated into a power plant incorporating MCFC units with suitable gas expansion turbines, steam turbines, heat exchangers, and heat recovery steam generators, using the Westinghouse proprietary AHEAD computer model; provide efficiency, investment, cost of electricity, operability, and environmental effect rankings of the system; and provide a final report incorporating the results of all of the above tasks. Section 7 of this final report provides general conclusions.

Jablonski, G.; Hamm, J.R.; Alvin, M.A.; Wenglarz, R.A.; Patel, P.

1982-01-01T23:59:59.000Z

373

Heat recovery device for exhaust flues  

SciTech Connect

The heat recovery device has a flue pipe assembly including a section of standard flue pipe carrying a plurality of hollow, cylindrical heating tubes extending diametrically through the flue pipe section in axially spaced, parallel relationship and a separate housing defining an air flow chamber surrounding a portion of the flue pipe section. A fan inside the housing draws ambient air into the housing through an ambient air inlet located on the same side of the flue pipe assembly as the inlet of the heating tubes and propels a flow of air both through the heating tubes and over the outer surface of the flue pipe section towards a heated air outlet located on the same side of the flue pipe section as the discharge ends of the heating tubes. The flue pipe assembly is removably mounted on the housing so it can be removed in the event it fatigues and/or becomes plugged with carbon or creosote deposits during use. A thermostat on the flue pipe section turns the fan on and off when the temperature in the flue pipe section is respectively above and below a predetermined temperature. The total open area of the ambient air inlet and the heated air outlet is large enough so that, in the event the fan is inoperative, the natural flow of ambient air through the heating tubes and over the outer surface of the flue pipe is sufficient to prevent the flue pipe section from overheating.

Knoch, D. G.

1985-11-05T23:59:59.000Z

374

Recombinant DNA encoding a desulfurization biocatalyst  

DOE Patents (OSTI)

This invention relates to a recombinant DNA molecule containing a gene or genes which encode a biocatalyst capable of desulfurizing a fossil fuel which contains organic sulfur molecules. For example, the present invention encompasses a recombinant DNA molecule containing a gene or genes of a strain of Rhodococcus rhodochrous.

Rambosek, John (Seattle, WA); Piddington, Chris S. (Seattle, WA); Kovacevich, Brian R. (Seattle, WA); Young, Kevin D. (Grand Forks, ND); Denome, Sylvia A. (Thompson, ND)

1994-01-01T23:59:59.000Z

375

Recombinant DNA encoding a desulfurization biocatalyst  

DOE Patents (OSTI)

This invention relates to a recombinant DNA molecule containing a gene or genes which encode a biocatalyst capable of desulfurizing a fossil fuel which contains organic sulfur molecules. For example, the present invention encompasses a recombinant DNA molecule containing a gene or genes of a strain of Rhodococcus rhodochrous. 13 figs.

Rambosek, J.; Piddington, C.S.; Kovacevich, B.R.; Young, K.D.; Denome, S.A.

1994-10-18T23:59:59.000Z

376

Hydrogen Sulfide, Oil and Gas, and People's Lana Skrtic  

E-Print Network (OSTI)

at sewage treatment plants, manure-handling plants, tanneries, and coke oven plants.5 2 EPA, "Report standard cubic feet)."9 Sour gas is routinely `sweetened' at processing facilities called desulfurization Process for Desulfurizing Ultra-deep Natural Gas Near the Wellhead," presented at Natural Gas Technologies

Kammen, Daniel M.

377

Understanding Corrosion Mechanisms  

E-Print Network (OSTI)

: Speigel (2006) + Corvino (2008) - Complicated: boiler OEMs have advantage - CO2 effect: Jülich, U. Pitt (unlikely, flue gas cools oxy-fired boiler) - options: cooling flue gas + de-sulfurization air-fire O2-fire

378

Enhanced durability and reactivity for zinc ferrite desulfurization sorbent. Volume 1, Bench-scale testing and analysis  

Science Conference Proceedings (OSTI)

AMAX Research & Development Center (AMAX R&D) has been investigating methods for enhancing the reactivity and durability of the zinc ferrite desulfurization sorbent. Zinc ferrite sorbents are intended for use in desulfurization of hot coal gas in integrated gasification combined cycle (IGCC) or molten carbonate fuel cell (MCFC) applications. For the present program, the reactivity of the sorbent may be defined as its sulfur sorption capacity at the breakthrough point and at saturation in a bench-scale, fixed-bed reactor. Durability may be defined as the ability of the sorbent to maintain important physical characteristics such As size, strength, and specific surface area during 10 cycles of sulfidation and oxidation.

Jha, M.C.; Berggren, M.H.

1989-05-02T23:59:59.000Z

379

Reactivity of target compounds for chemical coal desulfurization. Technical report, March 1, 1994--May 31, 1994  

SciTech Connect

This project seeks to identify representative organosulfur compounds which are removed by known coal desulfurization reactions. Demineralized coals are solvent extracted and the extracts fractionated to concentrate organosulfur compounds for analysis by Gas Chromatography/Mass Spectroscopy. After sulfur compounds are characterized, the parent extracts are subjected to reactions previously shown to reduce the organic sulfur content of Illinois coals, fractionated and again analyzed for organosulfur content to determine if the identified compounds reacted during the chemical treatment. The original coal also will be subjected to chemical desulfurization, extraction, fractionation and analysis in order to correlate changes in organic sulfur content of the coal with reactions of specific sulfur compounds. These compounds can thus be reliably considered as target molecules for the next generation of desulfurization processes. Work during this quarter has shown that fractionation and chromatography of pyridine extracts to isolate suitable samples for GC/MS analysis, although time-consuming, appears to be better than direct toluene extraction in terms of providing a representative set of compounds for analysis. The toluene soluble fractions prepared by this route contain aromatic sulfur compounds and O, N, S-containing hetrocycles. A set of these compounds has been identified and their fate following desulfurization of the parent coal extracts is under investigation. Previously studied desulfurization reactions using the single electron transfer reagent, K/THF/naphthalene, and the reactive nickel boride reagent have been repeated and analyzed by GC/MS. SET and nickel boride reactions of the THF soluble portions of pyridine coal are currently in progress.

Buchanan, D.H.; Amin, M.; Cunningham, R.; Galyen, J.; Ho, K.K.

1994-09-01T23:59:59.000Z

380

www.eia.gov  

U.S. Energy Information Administration (EIA)

Average Costs of Existing Flue Gas Desulfurization Units, 2007 - 2011 ... Average Installed Capital Costs (Dollars per Kilowatt) Note: Data for 2010 have been revised.

Note: This page contains sample records for the topic "flue gas desulfurization" 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

NETL F 451.1-1/1 Categorical Exclusion (CX) Designation Form  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

proprietary FMC Corporation technology to reduce NOx emissions and potentially reduce mercury using a spray dryer absorber flue gas desulfurization system. 03 18 2010 Andrew P....

382

Glossary - U.S. Energy Information Administration (EIA)  

U.S. Energy Information Administration (EIA)

Flue gas desulfurization: Equipment used to remove sulfur oxides from the combustion gases of a boiler plant before discharge to the atmosphere.

383

Development of Advanced Environmental Control Technology  

NLE Websites -- All DOE Office Websites (Extended Search)

mercury, on the other hand, is more readily captured because it is soluble in the liquids typically present in flue gas desulfurization scrubbers. Successful ionization of...

384

Power Technologies Energy Data Book: Fourth Edition, Chapter...  

NLE Websites -- All DOE Office Websites (Extended Search)

Table 9.7 - Environmental Compliance Equipment Costs (Nominal Dollars) 1990 1995 2000 2001 2002 2003 2004 Average Flue Gas Desulfurization Costs at Utilities Average Operation &...

385

NETL: Control Technology - Field Testing of a Wet FGD Additive...  

NLE Websites -- All DOE Office Websites (Extended Search)

Enhanced Mercury Control URS Corporation will demonstrate the use of an additive in wet lime or limestone flue gas desulfurization (FGD) systems to prevent oxidized mercury that...

386

SAS Output  

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

2. Quantity and Net Summer Capacity of Operable Environmental Equipment, 2001 - 2011 Flue Gas Desulfurization Systems Electrostatic Precipitators Baghouses Select Catalytic and...

387

U S  

NLE Websites -- All DOE Office Websites (Extended Search)

advantage of existing air pollution control devices, e.g., electrostatic precipitators (ESP), fabric filters, and flue gas desulfurization systems. With support from NETL, the...

388

DESULFURIZATION OF COAL MODEL COMPOUNDS AND COAL LIQUIDS  

E-Print Network (OSTI)

Pollutants Associated With Coal Combustion. • E.P.A.Control Guidelines for Coal-Derived Pollutants .Forms of Sulfur in Coal • . . . . Coal Desulfurization

Wrathall, James Anthony

2011-01-01T23:59:59.000Z

389

Enhanced durability and reactivity for zinc ferrite desulfurization sorbent  

Science Conference Proceedings (OSTI)

AMAX Research Development Center (AMAX R D) investigated methods for enhancing the reactivity and durability of zinc ferrite desulfurization sorbents. Zinc ferrite sorbents are intended for use in desulfurization of hot coal gas in integrated gasification combined cycle (IGCC) or molten carbonate fuel cell (MCFC) applications. For this program, the reactivity of the sorbent may be defined as its sulfur sorption capacity at the breakthrough point and at saturation in a bench-scale, fixed-bed reactor. Durability may be defined as the ability of the sorbent to maintain important physical characteristics such as size, strength, and specific surface area during 10 cycles of sulfidation and oxidation. Two base case sorbents, a spherical pellet and a cylindrical extrude used in related METC-sponsored projects, were used to provide a basis for the aimed enhancement in durability and reactivity. Sorbent performance was judged on the basis of physical properties, single particle kinetic studies based on thermogravimetric (TGA) techniques, and multicycle bench-scale testing of sorbents. A sorbent grading system was utilized to quantify the characteristics of the new sorbents prepared during the program. Significant enhancements in both reactivity and durability were achieved for the spherical pellet shape over the base case formulation. Overall improvements to reactivity and durability were also made to the cylindrical extrude shape. The primary variables which were investigated during the program included iron oxide type, zinc oxide:iron oxide ratio, inorganic binder concentration, organic binder concentration, and induration conditions. The effects of some variables were small or inconclusive. Based on TGA studies and bench-scale tests, induration conditions were found to be very significant.

Berggren, M.H.; Jha, M.C.

1989-10-01T23:59:59.000Z

390

Fundamental mechanisms in flue gas conditioning  

Science Conference Proceedings (OSTI)

We performed a wide variety of laboratory analyses during the past quarter. As with most of the work we performed during the previous quarter, our recent efforts were primarily directed toward the determination of the effects of adsorbed water on the cohesivity and tensile strength of powders. We also continued our analyses of dust cake ashes that have had the soluble compounds leached from their particle surfaces by repeated washings with water. Our analyses of leached and unleached dust cake ashes continued to provide some interesting insights into effects that compounds adsorbed on surfaces of ash particles can have on bulk ash behavior. As suggested by our literature review, our data indicate that water adsorption depends on particle morphology and on surface chemistry. Our measurements of tensile strength show, that for many of the samples we have analyzed a relative minimum in tensile strength exists for samples conditioned and tested at about 30% relative humidity. In our examinations of the effects of water conditioning on sample cohesivity, we determined that in the absence of absorption of water into the interior of the particles, cohesivity usually increases sharply when environments having relative humidities above 75% are used to condition and test the samples. Plans are under way to condition selected samples with (NH[sub 4])[sub 2]SO[sub 4], NH[sub 4]HSO[sub 4], CaCl[sub 2], organosiloxane, and SO[sub 3]. Pending approval, we will begin these conditioning experiments, and subsequent analyses of the conditioned samples.

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

1993-01-20T23:59:59.000Z

391

Fundamental mechanisms in flue gas conditioning  

Science Conference Proceedings (OSTI)

SEM pictures of the three mixtures of sorbent and ash from the DITF and the base line ESP hopper ash from Muskingum are shown in Figures 1 through 4. The effects of sorbent addition on particle morphology are evident in Figures 2 through 4 by the presence of irregularly shaped particles and deposits on the surfaces of the spherical fly ash particles. In contrast, the base Ene ash particles have the characteristic relatively smooth, spherical morphology normally associated with pulverized-coal (PC) fly ashes. Resistivity determinations made on these four ashes in ascending and descending temperature modes. These data are shown in Figures 5 and 6. Sorbent injection processes performed at the DITF lowered the duct temperature to around 165{degrees}F from about 350{degrees}F for base line operation. Consequently, during collection in the ESP, the particulate matter from the sorbent injection processes had a significantly lower resitivity (approximately 4 {times} 10{sup 7} {Omega}-cm) than the base line ash (approximately 3 {times} 10{sup 11} {Omega}-cm at 350{degrees}F). Specific surface areas and true particle densities have been measured for the four samples obtained from the DOE/PETC Duct Injection Test Facility. These data are summarized in Table 4. The primary difference indicated by these initial analyses of these four samples is the significant increase in specific surface area due to sorbent addition. The specific surface areas of the three sorbent and ash mixtures from the DITF are quite similar.

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

1992-07-27T23:59:59.000Z

392

Cement Kiln Flue Gas Recovery Scrubber Project  

NLE Websites -- All DOE Office Websites (Extended Search)

been expensive to simulate. Performance results were sufficiently promising to justify a commercial-scale test under the CCT program. A flowsheet of the Recovery Scrubber(tm) is...

393

NETL: Control Technology: Flue Gas Conditioning  

NLE Websites -- All DOE Office Websites (Extended Search)

a proven means of increasing the collection efficiency of an electrostatic precipitator (ESP). However, a new class of additives is needed because currently available agglomerating...

394

Development of a Desulfurization Strategy for a NOx Adsorber Catalyst  

DOE Green Energy (OSTI)

Improve NOx regeneration calibration developed in DECSE Phase I project to understand full potential of NOx adsorber catalyst over a range of operating temperatures. Develop and demonstrate a desulfurization process to restore NOx conversion efficiency lost to sulfur contamination. Investigate effect of desulfurization process on long-term performance of the NOx adsorber catalyst.

Tomazic, Dean

2000-08-20T23:59:59.000Z

395

Recovery of CO2 from Flue Gases: Commercial Trends  

NLE Websites -- All DOE Office Websites (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

396

Measurement of biocarbon in flue gases using 14C  

SciTech Connect

A preliminary investigation of the biocarbon fraction in carbon dioxide emissions of power plants using both fossil- and biobased fuels is presented. Calculation of the biocarbon fraction is based on radiocarbon content measured in power plant flue gases. Samples were collected directly from the chimneys into plastic sampling bags. The C-14 content in CO{sub 2} was measured by accelerator mass spectrometry (AMS). Flue gases from power plants that use natural gas, coal, wood chips, bark, plywood residue, sludge from the pulp factory, peat, and recovered fuel were measured. Among the selected plants, there was one that used only fossil fuel and one that used only biofuel; the other investigated plants burned mixtures of fuels. The results show that C-14 measurement provides the possibility to determine the ratio of bio and fossil fuel burned in power plants.

Haemaelaeinen, K.M.; Jungner, H.; Antson, O.; Rasanen, J.; Tormonen, K.; Roine, J. [University of Helsinki, Helsinki (Finland). Radiocarbon Dating Laboratory

2007-07-01T23:59:59.000Z

397

Edward S. Steinfeld Richard K. Lester  

E-Print Network (OSTI)

. The exceptions are 9 small units that burn oil, one that burns coke oven gas, and 13 that burn coal gangue in the combustion unit. In other cases, flue-gas desulfurization (FGD) systems, or "scrubbers," enabling post-combustion flue-gas desulfurization systems. Should Chinese environmental regulations strengthen in the near term

398

Enhanced durability of high-temperature desulfurization sorbents for moving-bed applications  

SciTech Connect

Sulfur removal will be mandatory for all power generation coal gas applications in order to comply with future environmental standards. Two promising technologies that are currently being optimized for coal-based power generation are the integrated gasification combined cycle (IGCC) and the gasifier/molten carbonate fuel cell (MCFC) systems. Zinc ferrite is currently the leading candidate to serve as a sulfur removal agent in the IGCC systems. GE has developed a patented moving-bed coal gas desulfurization system that has been shown to achieve a reduction in complexity and cost in a simplified IGCC system relative to conventional IGCC configurations (Cook et al, 1988).

Ayala, R.E. (GE Corporate Research and Development, Schenectady, NY (USA)); Gal, E. (GE Environmental Systems, Lebanon, PA (USA)); Gangwal, S.K. (Research Triangle Institute, NC (USA)); Jain, S. (Dept. of Energy, Morgantown, WV (USA))

1990-01-01T23:59:59.000Z

399

Method for the desulfurization of hot product gases from coal gasifier  

DOE Green Energy (OSTI)

The gasification of sulfur-bearing coal produces a synthesis gas which contains a considerable concentration of sulfur compounds especially hydrogen sulfide that renders the synthesis gas environmentally unacceptable unless the concentration of the sulfur compounds is significantly reduced. To provide for such a reduction in the sulfur compounds a calcium compound is added to the gasifier with the coal to provide some sulfur absorption. The synthesis gas from the gasifier contains sulfur compounds and is passed through an external bed of a regenerable solid absorbent, preferably zinc ferrite, for essentially completed desulfurizing the hot synthesis gas. This absorbent is, in turn, periodically or continuously regenerated by passing a mixture of steam and air or oxygen through the bed for converting absorbed hydrogen sulfide to sulfur dioxide. The resulting tail gas containing sulfur dioxide and steam is injected into the gasifier where the sulfur dioxide is converted by the calcium compound into a stable form of sulfur such as calcium sulfate.

Grindley, Thomas (Morgantown, WV)

1988-01-01T23:59:59.000Z

400

Method for the desulfurization of hot product gases from a coal gasifier  

DOE Patents (OSTI)

The gasification of sulfur-bearing coal produces a synthesis gas which contains a considerable concentration of sulfur compounds, especially hydrogen sulfide that renders the synthesis gas environmentally unacceptable unless the concentration of the sulfur compounds is significantly reduced. To provide for such a reduction in the sulfur compounds a calcium compound is added to the gasifier with the coal to provide some sulfur absorption. The synthesis gas from the gasifier contains sulfur compounds and is passed through an external bed of a regenerable solid absorbent, preferably zinc ferrite, for essentially completed desulfurizing the hot synthesis gas. This absorbent is, in turn, periodically or continuously regenerated by passing a mixture of steam and air or oxygen through the bed for converting absorbed hydrogen sulfide to sulfur dioxide. The resulting tail gas containing sulfur dioxide and steam is injected into the gasifier where the sulfur dioxide is converted by the calcium compound into a stable form of sulfur such as calcium sulfate. 2 figs.

Grindley, T.

1986-04-10T23:59:59.000Z

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401

Communications to the Editor Room-Temperature Desulfurization of  

E-Print Network (OSTI)

difficult to remove in the hydroprocessing of crude oil.3 In homogeneous models, orga- nometallic nickel of polynuclear complexes in the desulfurization of various thiophenes,6 led us to prepare a dinuclear nickel

Jones, William D.

402

High pressure ceramic air heater for indirectly fired gas turbine applications  

SciTech Connect

The EFCC cycle is conceptually simple. Air enters the compressor where it is pressurized and becomes the tube-side flow of the ceramic air heater. Heat transferred from the hot combustion gases flowing through the shell-side raises the air temperature to the desired turbine inlet temperature. Internally insulated high pressure piping returns the heated compressor air to the turbine, where it is expanded providing power to drive the electric generator and gas turbine compressor. Exhaust air from the turbine is used as the combustion air for the coal combustor. The EFCC cycle burns pulverized coal in an atmospheric combustion chamber similar to the combustion system in a conventional steam generator. The combustion gas exits the combustor and enters a slag screen, or impact separator, where the larger ash particles are collected to prevent fouling of the heat exchanger. After the slag screen, the combustion gas enters the shell-side of the CerHX where its thermal energy is transferred to the tube side air flow. Shell-side exit temperatures are sufficiently high to provide thermal energy for the bottoming Rankine Cycle through a heat recovery steam generator. Exhaust gas exiting the steam generator passes through a flue gas desulfurization system and a particulate removal system.

LaHaye, P.G.; Briggs, G.F.; Orozxo, N.J.; Seger, J.L.

1993-11-01T23:59:59.000Z

403

NETL: Clean Coal Technology Demonstration Program (CCTDP) - Round 2  

NLE Websites -- All DOE Office Websites (Extended Search)

Advanced Flue Gas Desulfurization Demonstration Project - Project Brief [PDF-250KB] Advanced Flue Gas Desulfurization Demonstration Project - Project Brief [PDF-250KB] Pure Air on the Lake L.P., Chesterton, IN PROGRAM PUBLICATIONS Final Reports Advanced Flue Gas Desulfurization (AFGD) Demonstration Project, Final Technical Report, Volume II: Project Performance and Economics [PDF-25MB] (Apr 1996) CCT Reports: Project Performance Summaries, Post-Project Assessments, & Topical Reports Advanced Flue Gas Desulfurization (AFGD) Demonstration Project: A DOE Assessment [PDF-235KB] (Aug 2001) Advanced Flue Gas Desulfurization Demonstration Project, Project Performance Summary [PDF-1.96MB] (June 1999) Advanced Technologies for the Control of Sulfur Dioxide Emissions from Coal-Fired Boilers, Topical Report No.12 [PDF-1.28MB] (June 1999) Design Reports

404

Effect of Environmental Parameters on the Performance of Coatings in FGD Ductwork  

Science Conference Proceedings (OSTI)

Coatings used in the outlet ducts of flue gas desulfurization (FGD) systems may fail prematurely. Research has shown that coating lifetime is a function of flue gas temperature and the concentration of some of the chemicals present in the flue gas condensate.

1993-04-01T23:59:59.000Z

405

CO2 Separation from Low-Temperature Flue Gases  

NLE Websites -- All DOE Office Websites (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

406

Predicting extents of mercury oxidation in coal-derived flue gases  

SciTech Connect

The extent of Hg oxidation determines the portion of Hg in the flue gas from a coal-fired power station that can be removed in SO{sub 2} scrubbers. This article evaluates predicted extents of Hg oxidation from a detailed chemical reaction mechanism, emphasizing the data from 1 and 29 MW pilotscale furnaces for diverse coal types. The proposed mercury (Hg) oxidation mechanism consists of a 168-step gas phase mechanism that accounts for interaction among all important flue gas species and a heterogeneous oxidation mechanism on unburned carbon (UBC) particles, similar to established chemistry for dioxin production under comparable conditions. The mechanism was incorporated into a gas cleaning system simulator to predict the proportions of elemental and oxidized Hg species in the flue gases, given relevant coal properties (C/H/O/N/S/Cl/Hg), flue gas composition (O{sub 2}, H{sub 2}O, HCl), emissions (NOx, SOx, CO), the recovery of fly ash, fly ash loss-on-ignition (LOI), and a thermal history. Predictions are validated without parameter adjustments against datasets from lab-scale and from pilot-scale coal furnaces at 1 and 29 MWt. Collectively, the evaluations cover 16 coals representing ranks from sub-bituminous through high-volatile bituminous, including cases with Cl{sub 2} and CaCl{sub 2} injection. The predictions are, therefore, validated over virtually the entire domain of Cl-species concentrations and UBC levels of comme