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1

CARBON TECHNOLOGY: I: Petroleum Coke  

Science Conference Proceedings (OSTI)

CARBON TECHNOLOGY: Session I: Petroleum Coke. Sponsored by: LMD Aluminum Committee Program Organizer: Jean-Claude Thomas , Aluminium ...

2

Adsorptive removal of nitrogen from coal-based needle coke feedstocks using activated carbon.  

E-Print Network (OSTI)

??A low percentage of nitrogen in needle coke feedstocks is desired for the reduction of puffing during the process of graphitization of needle coke. The… (more)

Madala, Sreeja.

2009-01-01T23:59:59.000Z

3

Strength of the coke fillers of carbon materials  

Science Conference Proceedings (OSTI)

Relationships between the ultimate compression strengths of coke fillers for carbon materials determined by various techniques and structures, final coke treatment temperatures, etc., are considered.

V.S. Ostrovskii [Research Institute of Structural Graphite Materials, Moscow (Russian Federation)

2008-12-15T23:59:59.000Z

4

Impurity Removal from Petroleum Coke - Programmaster.org  

Science Conference Proceedings (OSTI)

Presentation Title, Impurity Removal from Petroleum Coke. Author(s), Alexandre Gagnon, Hans Darmstadt, Nigel Backhouse, Esme Ryan, Laurence Dyer, David ...

5

Method for reducing coke oven carbonization pressure  

SciTech Connect

A method of reducing the carbonization pressure in the coking of coal is provided which comprises randomly dispersing flakes through the coal, said flakes formed of a material that does not pass through a plastic phase such as pressed sawdust wherein the flakes have a thickness of between about 1/8 '' and about 3/4 '' and a length and width of between about 1'' and about 5''.

Perch, M.

1981-04-28T23:59:59.000Z

6

Factors influencing coke gasification with carbon dioxide.  

E-Print Network (OSTI)

??Of all coke properties the influence of the catalytic mineral matter on reactivity of metallurgical cokes is least understood. There is limited information about the… (more)

Grigore, Mihaela

2007-01-01T23:59:59.000Z

7

Method for removing hydrogen sulfide from coke oven gas  

Science Conference Proceedings (OSTI)

An improved sulfur-ammonia process is disclosed for removing hydrogen sulfide from coke oven gases. In the improved process, a concentrator formerly used for standby operation is used at all normal times as an ammonia scrubber to improve the efficiency of gas separation during normal operation and is used as a concentrator for its intended standby functions during the alternative operations. In its normal function, the concentrator/scrubber functions as a scrubber to strip ammonia gas from recirculating liquid streams and to permit introduction of an ammonia-rich gas into a hydrogen sulfide scrubber to increase the separation efficiency of that unit. In the standby operation, the same concentrator/scrubber serves as a concentrator to concentrate hydrogen sulfide in a ''strong liquor'' stream for separate recovery as a strong liquor.

Ritter, H.

1982-08-03T23:59:59.000Z

8

Table 33. Coal Carbonized at Coke Plants by Census Division  

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

Coal Carbonized at Coke Plants by Census Division Coal Carbonized at Coke Plants by Census Division (thousand short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Table 33. Coal Carbonized at Coke Plants by Census Division (thousand short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Year to Date Census Division April - June 2013 January - March 2013 April - June 2012 2013 2012 Percent Change Middle Atlantic w w w w w w East North Central 3,051 2,997 3,092 6,048 6,156 -1.8 South Atlantic w w w w w w East South Central w w w w w w U.S. Total 5,471 5,280 5,296 10,751 10,579 1.6 w = Data withheld to avoid disclosure. Note: Total may not equal sum of components because of independent rounding. Source: U.S. Energy Information Administration (EIA), Form EIA-5, 'Quarterly Coal Consumption and Quality Report - Coke Plants

9

The use of ethylenediamine to remove hydrogen sulfide from coke oven gas  

Science Conference Proceedings (OSTI)

The investigations of the equilibrium absorption of H/sub 2/S by an EDA solution showed the solubility of hydrogen sulfide in ethylenediamine solutions is almost twice that in monoethanolamine solutions. Ethylenediamine may be used as an absorber for thorough removal of H/sub 2/S from coke oven gas in the presence of CO/sub 2/ and HCN. The hydrogen cyanide of coke oven gas, having practically no effect on the equilibrium absorption of H/sub 2/S and CO/sub 2/, may in this case be used in the form of ethylenethiourea - a marketable byproduct.

Marakhovskii, L.F.; Rezunenko, Y.I.; Popov, A.A.

1983-01-01T23:59:59.000Z

10

Use of ethylenediamine to remove hydrogen sulfide from coke oven gas  

SciTech Connect

The investigations of the equilibrium absorption of H/sub 2/S by an EDA solution which show that the solubility of hydrogen sulfide in ethylenediamine solutions is almost twice that in monoethanolamine solutions. Ethylenediamine may be used as an absorber for thorough removal of H/sub 2/S from coke oven gas in the presence of CO/sub 2/ and HCN. The hydrogen cyanide of coke oven gas, having practically no effect on the equilibrium absorption of H/sub 2/S and CO/sub 2/, may in this case be recovered in the form of ethylenethiourea - a marketable byproduct.

Marakhovskii, L.F.; Popov, A.A.; Rezunenko, Yu.I.

1983-01-01T23:59:59.000Z

11

CHARACTERIZATION OF COAL- AND PETROLEUM-DERIVED BINDER PITCHES AND THE INTERACTION OF PITCH/COKE MIXTURES IN PRE-BAKED CARBON ANODES.  

E-Print Network (OSTI)

??Carbon anodes are manufactured from calcined petroleum coke (i.e. sponge coke) and recycled anode butts as fillers, and coal tar pitch (SCTP) as the binder.… (more)

Suriyapraphadilok, Uthaiporn

2008-01-01T23:59:59.000Z

12

Design and operation of the coke-oven gas sulfur removal facility at Geneva Steel  

Science Conference Proceedings (OSTI)

The coke-oven gas sulfur removal facility at Geneva Steel utilizes a combination of two technologies which had never been used together. These two technologies had proven effective separately and now in combination. However, it brought unique operational considerations which has never been considered previously. The front end of the facility is a Sulfiban process. This monoethanolamine (MEA) process effectively absorbs hydrogen sulfide and other acid gases from coke-oven gas. The final step in sulfur removal uses a Lo-Cat II. The Lo-Cat process absorbs and subsequently oxidizes H{sub 2}S to elemental sulfur. These two processes have been effective in reducing sulfur dioxide emissions from coke-oven gas by 95%. Since the end of the start-up and optimization phase, emission rate has stayed below the 104.5 lb/hr limit of equivalent SO{sub 2} (based on a 24-hr average). In Jan. 1995, the emission rate from the sulfur removal facility averaged 86.7 lb/hr with less than 20 lb/hr from the Econobator exhaust. The challenges yet to be met are decreasing the operating expenses of the sulfur removal facility, notably chemical costs, and minimizing the impact of the heating system on unit reliability.

Havili, M.U.; Fraser-Smyth, L.L.; Wood, B.W. [Geneva Steel, Provo, UT (United States)

1996-02-01T23:59:59.000Z

13

An active carbon catalyst prevents coke formation from asphaltenes during the hydrocracking of vacuum residue  

SciTech Connect

Active carbons were prepared by the steam activation of a brown coal char. The active carbon with mesopores showed greater adsorption selectivity for asphaltenes. The active carbon was effective at suppressing coke formation, even with the high hydrocracking conversion of vacuum residue. The analysis of the change in the composition of saturates, aromatics, resins, and asphaltenes in the cracked residue with conversion demonstrated the ability of active carbon to restrict the transformation of asphaltenes to coke. The active carbon that was richer in mesopores was presumably more effective at providing adsorption sites for the hydrocarbon free-radicals generated initially during thermal cracking to prevent them from coupling and polycondensing.

Fukuyama, H.; Terai, S. [Toyo Engineering Corp., Chiba (Japan). Technological Research Center

2007-07-01T23:59:59.000Z

14

Dale Coke: Coke Farm  

E-Print Network (OSTI)

Dale Coke Photo by Benjamin J. Myers.2009. Coke FarmDale Coke grew up on an apricot orchard in California’s

Farmer, Ellen

2010-01-01T23:59:59.000Z

15

Electrochemical degradation characteristics of refractory organic pollutants in coking wastewater on multiwall carbon nanotube-modified electrode  

Science Conference Proceedings (OSTI)

The multiwall carbon nanotube-mollified electrode (MWCNT-ME) was fabricated and its electrocatalytic activity of refractory organic pollutants of coking wastewater was investigated. The surface morphology, absorption properties, and the electrochemical ...

Yan Wang; Shujing Sun; Guifu Ding; Hong Wang

2012-01-01T23:59:59.000Z

16

Investigation of the stress induced properties of coke during carbonization.  

E-Print Network (OSTI)

??The large polycyclic aromatic plates within coal tar pitches do not flow freely enough to organize into large anisotropic domains during pyrolytic carbonization. It was… (more)

Maybury, James Joshua.

2007-01-01T23:59:59.000Z

17

Carbon ion pump for removal of carbon dioxide from combustion ...  

Biomass and Biofuels; Building Energy Efficiency; ... Carbon ion pump for removal of carbon dioxide from combustion gas and other gas mixtures United States Patent ...

18

Problem of improving coke oven gas purification systems  

Science Conference Proceedings (OSTI)

A discussion of the problems of improving desulfurization processes of coke oven gas was presented. Of particular interest were control systems and increasing capacity of the coke ovens. Included in the discussion were the vacuum-carbonate and arsenic-soda sulfur removal systems. Problems involved with these systems were the number of treatment operations, the volume of the reagents used, and the operation of equipment for naphthalene and cyanide removal.

Goldin, I.A.

1982-01-01T23:59:59.000Z

19

Problem of sludge formation in benzol division solar oil and ''carbonization'' in coke oven gas compressor systems  

Science Conference Proceedings (OSTI)

A discussion is presented on the problem and possible causes of sludge formation in the return solar oil in benzene recovery units and on the problem of deposits in the pipe systems after coke oven gas compressors. The possible entrainment of fine particles of coal charge in the solar oil was also discussed. Sedimentation of the sludge was recommended with daily removal of the settled sludge. A chemical analysis of the deposits in the piping system of the coke oven gas and the coal charge revealed that the deposits were not caused by entrained coal particles. (JMT)

Rezunenko, Y.I.

1982-01-01T23:59:59.000Z

20

Development of a Filter Using Absorbent Technologies for the Removal of Coking Precursors: Laboratory Evaluation  

Science Conference Proceedings (OSTI)

On-load tap changers (LTC) are the single biggest contributor to transformer problems. Their failure modes may be mechanical, electrical, or related to the quality of the oil and contacts. Utilities are seeking new strategies for LTC maintenance to minimize these problems and, at the same time, reduce maintenance costs. EPRI has initiated several projects with a goal of producing a maintenance-free LTC. One major LTC problem is contact fouling, which can lead to the buildup of coke deposits on contacts a...

2003-11-24T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

Definition: Petroleum coke | Open Energy Information  

Open Energy Info (EERE)

coke coke Jump to: navigation, search Dictionary.png Petroleum coke A residue high in carbon content and low in hydrogen that is the final product of thermal decomposition in the condensation process in cracking (breaking of carbon-carbon bonds). This product is reported as marketable coke or catalyst coke.Coke from petroleum has a heating value of 6.024 million Btu per barrel.[1] View on Wikipedia Wikipedia Definition Petroleum coke (often abbreviated Pet coke or petcoke) is a carbonaceous solid derived from oil refinery coker units or other cracking processes. Other coke has traditionally been derived from coal. This coke can either be fuel grade (high in sulphur and metals) or anode grade (low in sulphur and metals). The raw coke directly out of the coker is often

22

Investigating factors that influence carbon dissolution from Coke into Molten iron.  

E-Print Network (OSTI)

??The need for more efficient blast furnaces is even greater now that there are stricter environmental regulations on greenhouse gas (GHG) emissions. Coke within the… (more)

Cham, S. Tsuey

2007-01-01T23:59:59.000Z

23

Preparation of Activated Carbon from Oil Sands Coke by Chemical and Physical Activation Techniques.  

E-Print Network (OSTI)

??Oil sands coke is a by-product resulting from the upgrading of heavy crude bitumen to light synthetic oil. This research investigates the preparation of activated… (more)

Morshed, Golam

2012-01-01T23:59:59.000Z

24

MOLECULAR COMPOSITION OF NEEDLE COKE FEEDSTOCKS AND MESOPHASE DEVELOPMENT DURING CARBONIZATION.  

E-Print Network (OSTI)

??This study investigates the molecular composition of fluid catalytic cracking (FCC) decant oil and its derivatives that are used as feedstocks for delayed coking to… (more)

Wang, Guohua

2005-01-01T23:59:59.000Z

25

Carbon Ion Pump for Carbon Dioxide Removal  

coal fired power plants; oil or gas fired power plants; cement production; bio-fuel combustion; Separation of carbon dioxide from other combustion ...

26

Postcombustion measures for cleaner solid fuels combustion: activated carbons for toxic pollutants removal from flue gases  

SciTech Connect

In this work the efficiency of postcombustion measures (i.e., activated carbon utilization) to achieve cleaner solid fuels combustion was evaluated. Thus, two commercial activated carbons (Calgon F400 and RWE active coke) were tested for removing toxic polluting compounds (Hg, PCBs, PCDD/Fs) from the gas phase. The effects of the pore structure and surface chemistry of the activated carbons tested were investigated, along with the sorption temperature and sulfur addition in carbon matrix. Experiments were realized in a bench-scale adsorption unit and in a commercial solid fuels-fired hot water boiler. The results showed that both activated carbons tested are suitable for the removal of toxic compounds (i.e., Hg, PCBs, PCDD/Fs) from the gas phase. Due to differences in Hg adsorptive capacity and adsorption rate, which are attributed to the diversified pore structure and surface chemistry of the activated carbons, RWE active coke is, presumably, more suitable for continuous Hg removal (i.e., activated carbon injection), while Calgon F400 is more suitable for batch one (packed column). For both activated carbons, Hg adsorption capacity was reduced with temperature increase, while it was enhanced by the presence of sulfur. Oxygen surface functional groups seem to be involved in Hg adsorption mechanism. Lactones are believed to act as potential active sites for mercury adsorption, while phenols may act as inhibitors. The removal of PCBs and PCDD/Fs from the gas phase seems not to be a problem for the activated carbons tested, regardless of their pore structure or surface chemistry. 61 refs., 23 figs., 8 tabs.

G. Skodras; I. Diamantopoulou; P. Natas; A. Palladas; G.P. Sakellaropoulos [Aristotle University of Thessaloniki, Thessaloniki (Greece). Chemical Process Engineering Laboratory, Department of Chemical Engineering

2005-12-01T23:59:59.000Z

27

Process for removing carbon from uranium  

DOE Patents (OSTI)

Carbon contamination is removed from uranium and uranium alloys by heating in inert atmosphere to 700.degree.-1900.degree.C in effective contact with yttrium to cause carbon in the uranium to react with the yttrium. The yttrium is either in direct contact with the contaminated uranium or in indirect contact by means of an intermediate transport medium.

Powell, George L. (Oak Ridge, TN); Holcombe, Jr., Cressie E. (Knoxville, TN)

1976-01-01T23:59:59.000Z

28

Innovative coke oven gas cleaning system for retrofit applications  

DOE Green Energy (OSTI)

The coke plant at the Sparrows Point Plant consist of three coke oven batteries and two coal chemical plants. The by-product coke oven gas (COG) consists primarily of hydrogen, methane, carbon monoxide, nitrogen and contaminants consisting of tars, light oils (benzene, toluene, and xylene) hydrogen sulfide, ammonia, water vapor and other hydrocarbons. This raw coke oven gas needs to be cleaned of most of its contaminants before it can be used as a fuel at other operations at the Sparrows Point Plant. In response to environmental concerns, BSC decided to replace much of the existing coke oven gas treatment facilities in the two coal chemical Plants (A and B) with a group of technologies consisting of: Secondary Cooling of the Coke oven Gas; Hydrogen Sulfide Removal; Ammonia Removal; Deacification of Acid Gases Removed; Ammonia Distillation and Destruction; and, Sulfur Recovery. This combination of technologies will replace the existing ammonia removal system, the final coolers, hydrogen sulfide removal system and the sulfur recovery system. The existing wastewater treatment, tar recovery and one of the three light oil recovery systems will continue to be used to support the new innovative combination of COG treatment technologies.

Not Available

1992-08-24T23:59:59.000Z

29

Coal Ash Carbon Removal Technologies  

Science Conference Proceedings (OSTI)

Market resistance to the use of ash containing elevated levels of carbon and/or ammonia has become a major concern for coal-fired facilities in recent years as a result of increased use of nitrogen oxide (NOx) reduction environmental control technologies. EPRI initiated this state of practice assessment to help power producers evaluate alternatives for ash beneficiation.

2001-11-01T23:59:59.000Z

30

Study of Modified Semi-Coke on the Advanced Treatment of Coking ...  

Science Conference Proceedings (OSTI)

Mass of absorbent and absorption time had put much on the removal rate of oil in coke wastewater. The removal rate of oil in coke wastewater could be above ...

31

Study on the effect of heat treatment and gasification on the carbon structure of coal chars and metallurgical cokes using fourier transform Raman spectroscopy  

Science Conference Proceedings (OSTI)

Differences in the development of carbon structures between coal chars and metallurgical cokes during high-temperature reactions have been investigated using Raman spectroscopy. These are important to differentiate between different types of carbons in dust recovered from the top gas of the blast furnace. Coal chars have been prepared from a typical injectant coal under different heat-treatment conditions. These chars reflected the effect of peak temperature, residence time at peak temperature, heating rate and pressure on the evolution of their carbon structures. The independent effect of gasification on the development of the carbon structure of a representative coal char has also been studied. A similar investigation has also been carried out to study the effect of heat-treatment temperature (from 1300 to 2000{sup o}C) and gasification on the carbon structure of a typical metallurgical coke. Two Raman spectral parameters, the intensity ratio of the D band to the G band (I{sub D}/I{sub G}) and the intensity ratio of the valley between D and G bands to the G band (I{sub V}/I{sub G}), have been found useful in assessing changes in carbon structure. An increase in I{sub D}/I{sub G} indicates the growth of basic graphene structural units across the temperature range studied. A decrease in I{sub V}/I{sub G} appears to suggest the elimination of amorphous carbonaceous materials and ordering of the overall carbon structure. The Raman spectral differences observed between coal chars and metallurgical cokes are considered to result from the difference in the time-temperature history between the raw injectant coal and the metallurgical coke and may lay the basis for differentiation between metallurgical coke fines and coal char residues present in the dust carried over the top of the blast furnace. 41 refs., 17 figs., 3 tabs.

S. Dong; P. Alvarez; N. Paterson; D.R. Dugwell; R. Kandiyoti [Imperial College London, London (United Kingdom). Department of Chemical Engineering

2009-03-15T23:59:59.000Z

32

Final environmental information volume for the coke oven gas cleaning project at the Bethlehem Steel Corporation Sparrows Point Plant  

Science Conference Proceedings (OSTI)

Bethelehem Steel Corporation (BSC) is planning to conduct a demonstration project involving an integrated system that can be retrofitted into coke oven gas handling systems to address a variety of environmental and operational factors in a more cost-effective manner. Successful application of this technology to existing US coke plants could: (1) reduce emissions of sulfur dioxide, cyanide, and volatile organic compounds (including benzene) (2) reduce the cost and handling of processing feed chemicals, (3) disposal costs of nuisance by-products and (4) increase reliability and reduce operation/maintenance requirements for coke oven gas desulfurization systems. The proposed system will remove sulfur from the coke oven gas in the form of hydrogen sulfide using the ammonia indigenous to the gas as the primary reactive chemical. Ammonia and hydrogen cyanide are also removed in this process. The hydrogen sulfide removed from the coke oven gas in routed to a modified Claus plant for conversion to a saleable sulfur by-product. Ammonia and hydrogen cyanide will be catalytically converted to hydrogen, nitrogen, carbon dioxide, and carbon monoxide. The tail gas from the sulfur recovery unit is recycled to the coke oven gas stream, upstream of the new gas cleaning system. The proposed demonstration project will be installed at the existing coke oven facilities at BSC's Sparrows Point Plant. This volume describes the proposed actions and the resulting environmental impacts. 21 refs., 19 figs., 9 tabs.

Not Available

1990-04-24T23:59:59.000Z

33

Organoclay Sorbent for Removal of Carbon Dioxide from Gas ...  

Organoclay Sorbent for Removal of Carbon Dioxide from Gas ... required for sequestration, an area of research identified as a high priority

34

Determination of electrical resistivity of dry coke beds  

SciTech Connect

The electrical resistivity of the coke bed is of great importance when producing FeMn, SiMn, and FeCr in a submerged arc furnace. In these processes, a coke bed is situated below and around the electrode tip and consists of metallurgical coke, slag, gas, and metal droplets. Since the basic mechanisms determining the electrical resistivity of a coke bed is not yet fully understood, this investigation is focused on the resistivity of dry coke beds consisting of different carbonaceous materials, i.e., coke beds containing no slag or metal. A method that reliably compares the electrical bulk resistivity of different metallurgical cokes at 1500{sup o} C to 1600{sup o}C is developed. The apparatus is dimensioned for industrial sized materials, and the electrical resistivity of anthracite, charcoal, petroleum coke, and metallurgical coke has been measured. The resistivity at high temperatures of the Magnitogorsk coke, which has the highest resistivity of the metallurgical cokes investigated, is twice the resistivity of the Corus coke, which has the lowest electrical resistivity. Zdzieszowice and SSAB coke sort in between with decreasing resistivities in the respective order. The electrical resistivity of anthracite, charcoal, and petroleum coke is generally higher than the resistivity of the metallurgical cokes, ranging from about two to about eight times the resistivity of the Corus coke at 1450{sup o}C. The general trend is that the bulk resistivity of carbon materials decreases with increasing temperature and increasing particle size.

Eidem, P.A.; Tangstad, M.; Bakken, J.A. [NTNU, Trondheim (Norway)

2008-02-15T23:59:59.000Z

35

Price of dwindling supply of better-quality coke will trend upward during this decade  

Science Conference Proceedings (OSTI)

This paper discusses the markets for petroleum coke with particular emphasis on the USA. The factors affecting the price of Green Coke are examined. It is considered that the price of any coke is set by the mix of markets available to the market based on demand. However, refiners producing similar quality cokes, will not necessarily receive the same netback price even if their cokes are sold to the same mix of markets. Calcined coke is used almost exclusively by the Aluminium industry thus green coke prices are indirectly tied to those of Aluminium as green coke is the primary carbon source for the calcined coke market.

Fasullo, P.; Tarrillion, T.; Matson, J.

1982-11-08T23:59:59.000Z

36

Method of removing carbon monoxide from gases  

DOE Patents (OSTI)

A process and catalyst are disclosed for purifying an atmosphere containing carbon monoxide by passing the atmosphere through a bed of a catalyst of TbO.sub.x, where x = 1.8 to 1.5, which oxidizes the carbon monoxide to carbon dioxide.

Gerstein, Bernard C. (Ames, IA); Macaulay, David B. (Arlington Heights, IL)

1976-06-01T23:59:59.000Z

37

Metal Organic Clathrates for Carbon Dioxide Removal  

removal from coal-fired power plant flue gas streams.  Modified variations of the materials can be used in a variety of other fields as well, ...

38

Promotion of Water-mediated Carbon Removal by Nanostructured Barium Oxide/nickel Interfaces  

DOE Green Energy (OSTI)

The existing Ni-yttria-stabilized zirconia anodes in solid oxide fuel cells (SOFCs) perform poorly in carbon-containing fuels because of coking and deactivation at desired operating temperatures. Here we report a new anode with nanostructured barium oxide/nickel (BaO/Ni) interfaces for low-cost SOFCs, demonstrating high power density and stability in C{sub 3}H{sub 8}, CO and gasified carbon fuels at 750 C. Synchrotron-based X-ray analyses and microscopy reveal that nanosized BaO islands grow on the Ni surface, creating numerous nanostructured BaO/Ni interfaces that readily adsorb water and facilitate water-mediated carbon removal reactions. Density functional theory calculations predict that the dissociated OH from H2O on BaO reacts with C on Ni near the BaO/Ni interface to produce CO and H species, which are then electrochemically oxidized at the triple-phase boundaries of the anode. This anode offers potential for ushering in a new generation of SOFCs for efficient, low-emission conversion of readily available fuels to electricity.

L Yang; Y Choi; W Qin; H Chen; K Blinn; M Liu; P Liu; J Bai; T Tyson; M Liu

2011-12-31T23:59:59.000Z

39

Integrated coke, asphalt and jet fuel production process and apparatus  

DOE Patents (OSTI)

A process and apparatus for the production of coke, asphalt and jet fuel from a feed of fossil fuels containing volatile carbon compounds therein is disclosed. The process includes the steps of pyrolyzing the feed in an entrained bed pyrolyzing means, separating the volatile pyrolysis products from the solid pyrolysis products, removing at least some coke from the solid pyrolysis products, fractionating the volatile pyrolysis products to produce an overhead stream and a bottom stream which is useful as asphalt for road pavement, condensing the overhead stream to produce a condensed liquid fraction and a noncondensable, gaseous fraction, and removing water from the condensed liquid fraction to produce a jet fuel-containing product. The disclosed apparatus is useful for practicing the foregoing process. The process provides a useful method of mass producing these products from materials such as coal, oil shale and tar sands. 1 fig.

Shang, Jer Yu.

1989-10-17T23:59:59.000Z

40

Integrated coke, asphalt and jet fuel production process and apparatus  

DOE Patents (OSTI)

A process and apparatus for the production of coke, asphalt and jet fuel m a feed of fossil fuels containing volatile carbon compounds therein is disclosed. The process includes the steps of pyrolyzing the feed in an entrained bed pyrolyzing means, separating the volatile pyrolysis products from the solid pyrolysis products removing at least one coke from the solid pyrolysis products, fractionating the volatile pyrolysis products to produce an overhead stream and a bottom stream which is useful as asphalt for road pavement, condensing the overhead stream to produce a condensed liquid fraction and a noncondensable, gaseous fraction, and removing water from the condensed liquid fraction to produce a jet fuel-containing product. The disclosed apparatus is useful for practicing the foregoing process. the process provides a useful method of mass producing and jet fuels from materials such as coal, oil shale and tar sands.

Shang, Jer Y. (McLean, VA)

1991-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

Petroleum Coke VBD  

Science Conference Proceedings (OSTI)

Mar 1, 2011 ... Electrode Technology for Aluminium Production: Petroleum Coke VBD ... of Calcined Petroleum Coke: Jignesh Panchal1; Mark Wyborney1; ...

42

New packing in absorption systems for trapping benzene from coke-oven gas  

SciTech Connect

The efficiency of benzene removal from coke-oven gas in absorption units OAO Alchevskkoks with new packing is assessed.

V.V. Grabko; V.M. Li; T.A. Shevchenko; M.A. Solov'ev [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

43

Carbon Ion Pump for Carbon Dioxide Removal - Energy Innovation ...  

coal fired power plants; oil or gas fired power plants; cement production; bio-fuel combustion; Separation of carbon dioxide from other combustion ...

44

Coke briquettes  

SciTech Connect

This patent describes a briquette suitable for use as an auxiliary fuel in a shaft furnace for melting of mineral in the manufacture of mineral wool which comprises: 30-75% by weight, based on the dry weight of the briquettes, of particles of coke fines or coal fines or both, the fines consisting essentially of particles having a particle size of from 2 to 25 mm; at least 7% by weight, based on the dry weight of the briquette, of a hydraulic binder; and at least 15% by weight, based on the dry weight of the briquette, of a fine grain oxidic mineral component selected from the group consisting of sand, slag, stone powder, fly ash, limestone powder, dolomite powder, silicon dioxide, and waste material from mineral wool manufacturer, the fine grain oxidic mineral component having a particle size of less than 2 mm.

Anderson, D.B.; Juhlin, N.J.W.; Gillenium, C.I.; Kjell-Berger, O.; Brinck, O.R.

1987-04-28T23:59:59.000Z

45

Innovative coke oven gas cleaning system for retrofit applications. Quarterly environmental monitoring report No. 1, January 1, 1991--June 30, 1991  

DOE Green Energy (OSTI)

The coke plant at the Sparrows Point Plant consist of three coke oven batteries and two coal chemical plants. The by-product coke oven gas (COG) consists primarily of hydrogen, methane, carbon monoxide, nitrogen and contaminants consisting of tars, light oils (benzene, toluene, and xylene) hydrogen sulfide, ammonia, water vapor and other hydrocarbons. This raw coke oven gas needs to be cleaned of most of its contaminants before it can be used as a fuel at other operations at the Sparrows Point Plant. In response to environmental concerns, BSC decided to replace much of the existing coke oven gas treatment facilities in the two coal chemical Plants (A and B) with a group of technologies consisting of: Secondary Cooling of the Coke oven Gas; Hydrogen Sulfide Removal; Ammonia Removal; Deacification of Acid Gases Removed; Ammonia Distillation and Destruction; and, Sulfur Recovery. This combination of technologies will replace the existing ammonia removal system, the final coolers, hydrogen sulfide removal system and the sulfur recovery system. The existing wastewater treatment, tar recovery and one of the three light oil recovery systems will continue to be used to support the new innovative combination of COG treatment technologies.

Not Available

1992-08-24T23:59:59.000Z

46

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

DOE Patents (OSTI)

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

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

2010-11-09T23:59:59.000Z

47

Influence of Petroleum Coke Sulphur Content on the Sodium ... - TMS  

Science Conference Proceedings (OSTI)

Feb 1, 1993 ... Influence of Petroleum Coke Sulphur Content on the Sodium Sensitivity of Carbon Anodes by S.M. Hume ... TMS Student Member price: 0.00.

48

Comparison of the Potential Impacts of Petroleum Coke and Anthracite Culm Use  

E-Print Network (OSTI)

The primary feedstock for the proposed Gilberton Coal-to-Clean Fuels and Power Project would be low-cost anthracite culm, which is a locally abundant, previously discarded resource that could accommodate fuel requirements during the demonstration period. Culm reserves controlled by WMPI are estimated to be sufficient to supply the proposed facilities for about 15 years, or to supply both the proposed facilities and the existing Gilberton Power Plant for about 11 years. Based on the applicant’s proposal, the facilities would also be capable of using a blend of feedstock containing up to 25% petroleum coke. Petroleum coke is a high-sulfur, high-energy product having the appearance of coal. Oil refineries produce petroleum coke by heating and removing volatile organic compounds (VOCs) from the residue remaining after the refining process. This appendix compares some of the potential impacts of 100 % anthracite culm use with the potential impacts from using a blended feedstock of 75 % anthracite culm and 25 % petroleum coke. Topics considered include carbon dioxide emissions, air emissions of sulfur compounds and toxic substances, solid wastes and byproduct production, and increased truck traffic. Carbon Dioxide (CO2) Emissions Published values for potential CO2 emissions from anthracite and petroleum coke are very similar.

Gilberton Coal-to-clean Fuels

2007-01-01T23:59:59.000Z

49

Method for processing coke oven gas  

SciTech Connect

Coke oven gas is subjected, immediately after the discharge thereof from coke ovens, and without any preliminary cooling operation or any purification operation other than desulfurization, to a catalytic cracking operation to form a hot cracked gas which is rich in hydrogen and carbon monoxide. The catalytic cracking reaction is carried out in the presence of a hydrogen-containing and/or CO2-containing gas, with a steam reforming catalyst.

Flockenhaus, C.; Meckel, J.F.; Wagener, D.

1980-11-25T23:59:59.000Z

50

Investigation of bonding mechanism of coking on semi-coke from lignite with pitch and tar  

SciTech Connect

In coking, the bonding ability of inert macerals by reactive macerals is dependent on various parameters and also is related to the wettability of the inert macerals. In this study, the effect of carbonization temperature on the wettability of semi-cokes produced at various temperatures has been investigated. Soma and Yatagan semicokes represent inert macerals, and pitch was used as a reactive structure in the experiments. The briquetted pitch blocks were located on the semi-cokes and heated from the softening temperature of pitch (60{sup o}C) to 140{sup o}C to observe the wettability. In addition, liquid tar was also used to determine the wettability of semi-cokes. From the standpoint of wettability, the temperature of 900{sup o}C was determined to be the critical point for coke produced from sub-bituminous coals. 15 refs., 6 figs., 2 tabs.

Vedat Arslan [Dokuz Eylul University, Izmir (Turkey). Engineering Faculty

2006-10-15T23:59:59.000Z

51

Reducing Power Production Costs by Utilizing Petroleum Coke  

Science Conference Proceedings (OSTI)

Petroleum coke, a byproduct of the petroleum-refining process, is an attractive primary or supplemental fuel for power production primarily because of a progressive and predictable increase in the production volumes of petroleum coke. It is most commonly blended with coal in proportions suitable to meet sulfur emission compliance, and is generally less reactive than coal. Therefore, the cofiring of petroleum coke with coal typically improves ignition, flame stability, and carbon loss relative to the comb...

2000-05-05T23:59:59.000Z

52

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

53

REDUCING POWER PRODUCTION COSTS BY UTILIZING PETROLEUM COKE  

Science Conference Proceedings (OSTI)

Petroleum coke, a byproduct of the petroleum-refining process, is an attractive primary or supplemental fuel for power production primarily because of a progressive and predictable increase in the production volumes of petroleum coke (1, 2). Petroleum coke is most commonly blended with coal in proportions suitable to meet sulfur emission compliance. Petroleum coke is generally less reactive than coal; therefore, the cofiring of petroleum coke with coal typically improves ignition, flame stability, and carbon loss relative to the combustion of petroleum coke alone. Although petroleum coke is a desirable fuel for producing relatively inexpensive electrical power, concerns about the effects of petroleum coke blending on combustion and pollution control processes exist in the coal-fired utility industry (3). The Energy & Environmental Research Center (EERC) completed a 2-year technical assessment of petroleum coke as a supplemental fuel. A survey questionnaire was sent to seven electric utility companies that are currently cofiring coal and petroleum coke in an effort to solicit specific suggestions on research needs and fuel selections. An example of the letter and survey questionnaire is presented in Appendix A. Interest was expressed by most utilities in evaluating the effects of petroleum coke blending on grindability, combustion reactivity, fouling, slagging, and fly ash emissions control. Unexpectedly, concern over corrosion was not expressed by the utilities contacted. Although all seven utilities responded to the question, only two utilities, Northern States Power Company (NSP) and Ameren, sent fuels to the EERC for evaluation. Both utilities sent subbituminous coals from the Power River Basin and petroleum shot coke samples. Petroleum shot coke is produced unintentionally during operational upsets in the petroleum refining process. This report evaluates the effects of petroleum shot coke blending on grindability, fuel reactivity, fouling/slagging, and electrostatic precipitator (ESP) fly ash collection efficiency.

Kevin C. Galbreath; Donald L. Toman; Christopher J. Zygarlicke

1999-09-01T23:59:59.000Z

54

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

55

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 ...

56

Fundamentals of Delayed Coking Joint Industry Project  

SciTech Connect

Delayed coking evolved steadily over the early to mid 1900s to enable refiners to convert high boiling, residual petroleum fractions to light products such as gasoline. Pound for pound, coking is the most energy intensive of any operation in a modern refinery. Large amounts of energy are required to heat the thick, poor-quality petroleum residuum to the 900 to 950 degrees F required to crack the heavy hydrocarbon molecules into lighter, more valuable products. One common misconception of delayed coking is that the product coke is a disadvantage. Although coke is a low valued (near zero economic value) byproduct, compared to transportation fuels, there is a significant worldwide trade and demand for coke as it is an economical fuel. Coke production has increased steadily over the last ten years, with further increases forecast for the foreseeable future. Current domestic production is near 111,000 tons per day. A major driving force behind this increase is the steady decline in crude quality available to refiners. Crude slates are expected to grow heavier with higher sulfur contents while environmental restrictions are expected to significantly reduce the demand for high-sulfur residual fuel oil. Light sweet crudes will continue to be available and in even greater demand than they are today. Refiners will be faced with the choice of purchasing light sweet crudes at a premium price, or adding bottom of the barrel upgrading capability, through additional new investments, to reduce the production of high-sulfur residual fuel oil and increase the production of low-sulfur distillate fuels. A second disadvantage is that liquid products from cokers frequently are unstable, i.e., they rapidly form gum and sediments. Because of intermediate investment and operating costs, delayed coking has increased in popularity among refiners worldwide. Based on the 2000 Worldwide Refining Survey published in the Oil and Gas, the delayed coking capacity for 101 refineries around the world is 2,937,439 barrels/calendar day. These cokers produce 154,607 tons of coke per day and delayed coking accounts for 88% of the world capacity. The delayed coking charge capacity in the United States is 1,787,860 b/cd. Despite its wide commercial use, only relatively few contractors and refiners are truly knowledgeable in delayed-coking design, so that this process carries with it a ''black art'' connotation. Until recently, the expected yield from cokers was determined by a simple laboratory test on the feedstock. As a result of Tulsa University's prior related research, a process model was developed that with additional work could be used to optimize existing delayed cokers over a wide range of potential feedstocks and operating conditions. The objectives of this research program are to: utilize the current micro, batch and pilot unit facilities at The University of Tulsa to enhance the understanding of the coking process; conduct additional micro and pilot unit tests with new and in-house resids and recycles to make current optimization models more robust; conduct focused kinetic experiments to enhance the furnace tube model and to enhance liquid production while minimizing sulfur in the products; conduct detailed foaming studies to optimize the process and minimize process upsets; quantify the parameters that affect coke morphology; and to utilize the knowledge gained from the experimental and modeling studies to enhance the computer programs developed in the previous JIP for optimization of the coking process. These refined computer models will then be tested against refinery data provided by the member companies. Novel concepts will also be explored for hydrogen sulfide removal of furnace gases as well as gas injection studies to reduce over-cracking.

Michael Volk; Keith Wisecarver

2004-09-26T23:59:59.000Z

57

Fundamentals of Delayed Coking Joint Industry Project  

SciTech Connect

Delayed coking evolved steadily over the early to mid 1900s to enable refiners to convert high boiling, residual petroleum fractions to light products such as gasoline. Pound for pound, coking is the most energy intensive of any operation in a modern refinery. Large amounts of energy are required to heat the thick, poor-quality petroleum residuum to the 900 to 950 degrees F required to crack the heavy hydrocarbon molecules into lighter, more valuable products. One common misconception of delayed coking is that the product coke is a disadvantage. Although coke is a low valued (near zero economic value) byproduct, compared to transportation fuels, there is a significant worldwide trade and demand for coke as it is an economical fuel. Coke production has increased steadily over the last ten years, with further increases forecast for the foreseeable future. Current domestic production is near 111,000 tons per day. A major driving force behind this increase is the steady decline in crude quality available to refiners. Crude slates are expected to grow heavier with higher sulfur contents while environmental restrictions are expected to significantly reduce the demand for high-sulfur residual fuel oil. Light sweet crudes will continue to be available and in even greater demand than they are today. Refiners will be faced with the choice of purchasing light sweet crudes at a premium price, or adding bottom of the barrel upgrading capability, through additional new investments, to reduce the production of high-sulfur residual fuel oil and increase the production of low-sulfur distillate fuels. A second disadvantage is that liquid products from cokers frequently are unstable, i.e., they rapidly form gum and sediments. Because of intermediate investment and operating costs, delayed coking has increased in popularity among refiners worldwide. Based on the 2000 Worldwide Refining Survey published in the Oil and Gas, the delayed coking capacity for 101 refineries around the world is 2,937,439 barrels/calendar day. These cokers produce 154,607 tons of coke per day and delayed coking accounts for 88% of the world capacity. The delayed coking charge capacity in the United States is 1,787,860 b/cd. Despite its wide commercial use, only relatively few contractors and refiners are truly knowledgeable in delayed-coking design, so that this process carries with it a ''black art'' connotation. Until recently, the expected yield from cokers was determined by a simple laboratory test on the feedstock. As a result of Tulsa University's prior related research, a process model was developed that with additional work could be used to optimize existing delayed cokers over a wide range of potential feedstocks and operating conditions. The objectives of this research program are to: utilize the current micro, batch and pilot unit facilities at The University of Tulsa to enhance the understanding of the coking process; conduct additional micro and pilot unit tests with new and in-house resids and recycles to make current optimization models more robust; conduct focused kinetic experiments to enhance the furnace tube model and to enhance liquid production while minimizing sulfur in the products; conduct detailed foaming studies to optimize the process and minimize process upsets; quantify the parameters that affect coke morphology; and to utilize the knowledge gained from the experimental and modeling studies to enhance the computer programs developed in the previous JIP for optimization of the coking process. These refined computer models will then be tested against refinery data provided by the member companies. Novel concepts will also be explored for hydrogen sulfide removal of furnace gases as well as gas injection studies to reduce over-cracking.

Michael Volk; Keith Wisecarver

2003-09-26T23:59:59.000Z

58

Water protection in coke-plant design  

Science Conference Proceedings (OSTI)

Wastewater generation, water consumption, and water management at coke plants are considered. Measures to create runoff-free water-supply and sewer systems are discussed. Filters for water purification, corrosion inhibitors, and biocides are described. An integrated single-phase technology for the removal of phenols, thiocyanides, and ammoniacal nitrogen is outlined.

G.I. Alekseev [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

59

Simulation of Combustion and Thermal-flow Inside a Petroleum Coke Rotary Calcining Kiln.  

E-Print Network (OSTI)

??Calcined coke is the best material for making carbon anodes for smelting of alumina to aluminum. Calcining is an energy intensive industry and a significant… (more)

Zhang, Zexuan

2007-01-01T23:59:59.000Z

60

Effect of Blending HDPE with Coke on the Reduction Behavior of a ...  

Science Conference Proceedings (OSTI)

This has led to the exploration of the possibility of using polymer/coke blends in the production of ferro-alloys, particularly High Carbon Ferromanganese (HC ...

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


61

The effect of diabietic acid on the coking of oxidised solvent-extracted coal.  

E-Print Network (OSTI)

??Refcoal is a refined carbon source obtained by extraction of coal with dimethylformamide (DMF). During the coking process, Refcoal goes through a mesophase (fluid) stage… (more)

Ludere, Margaret Tshimangadzo

2008-01-01T23:59:59.000Z

62

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

63

Enhancing As sup 5+ removal by a Fe sup 2+ -treated activated carbon  

SciTech Connect

The effectiveness of pretreating an activated carbon with iron-salt solution to improve its arsenic removal capacity was studied. Various factors such as type and concentration of salt, pH, and treating time were thoroughly investigated for their effects on the improvement of removal capacity. An effort was made to identify the optimal pretreatment conditions. A ten-fold increase, over the untreated activated carbon, in removal can be achieved under the optimal pretreatment procedure. The enhancement in removal by treatment occurs by adsorption of ferrous ions and formation of arsenate complexes. Ferrous salts can also be used to regenerate the activated carbon.

Huang, C.P.; Vane, L.M.

1989-09-01T23:59:59.000Z

64

Perchlorate ion (C104) removal using an electrochemically induced catalytic reaction on modified activated carbon  

E-Print Network (OSTI)

Perchlorate is known to adversely affect the thyroid gland functions including iodide take up, thus perchlorate should be removed from drinking water. Bituminous coal-based activated carbon (AC) has been used for perchlorate removal in past years. Virgin carbon and carbon modified by oxidation with HNO3, NaOH and H2O2 were examined in this study for their ability to remove perchlorate by reduction or adsorption mechanisms. Surface functional groups formed on the modified AC (MAC) were examined with diffuse reflectance infrared spectrometry. Inhibition of perchlorate removal onto MAC by various anions ( - Cl , - 3 NO , and - 2 4 SO ) and solution pH (4.5, 7.2 and 10.5) were examined to characterize the MACs before an electrochemical reaction was performed. Surface functional groups were increased by oxidation. Groups that were found on the carbon include, but are not limited to lactone, quinine, carboxylate, and nitrogenoxygen groups. The effect of pH on removal of perchlorate by MAC was greatly affected by the change in the zero point charge (ZPC) induced on the carbon by modification. Virgin carbon also experienced difficulty in removing perchlorate when solution pH was above the ZPC. Anion inhibition varied with the modification process. - 3 NO inhibited perchlorate removal only by the virgin carbon. The other anions showed no major effects on the removal efficiency of perchlorate by the carbons. Electrochemical processes did not show favorable results in removal of perchlorate. The dominant mechanism of perchlorate removal during desorption tests was adsorption onto the carbon surfaces via ion exchange.

Langille, Meredith Caitlyn

2006-12-01T23:59:59.000Z

65

Dry purification of aspirational air in coke-sorting systems with wet slaking of coke  

Science Conference Proceedings (OSTI)

Coke transportation after wet slaking is accompanied by the release of dust in the production building and in the surrounding atmosphere. Wet methods are traditionally used to purify very humid air. Giprokoks has developed designs for highly efficient dry dust-removal methods in such conditions.

T.F. Trembach; A.G. Klimenko [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

66

Slurried solid media for simultaneous water purification and carbon dioxide removal from gas mixtures  

Science Conference Proceedings (OSTI)

A slurried solid media for simultaneous water purification and carbon dioxide removal from gas mixtures includes the steps of dissolving the gas mixture and carbon dioxide in water providing a gas, carbon dioxide, water mixture; adding a porous solid media to the gas, carbon dioxide, water mixture forming a slurry of gas, carbon dioxide, water, and porous solid media; heating the slurry of gas, carbon dioxide, water, and porous solid media producing steam; and cooling the steam to produce purified water and carbon dioxide.

Aines, Roger D.; Bourcier, William L.; Viani, Brian

2013-01-29T23:59:59.000Z

67

Definition: Coke | Open Energy Information  

Open Energy Info (EERE)

Coke A solid carbonaceous residue derived from low-ash, low-sulfur bituminous coal; used as a fuel and a reducing agent in smelting iron ore in a blast furnace. Coke from...

68

Met coke world summit 2005  

SciTech Connect

Papers are presented under the following session headings: industry overview and market outlook; coke in the Americas; the global coke industry; and new developments. All the papers (except one) only consist of a copy of the overheads/viewgraphs.

NONE

2005-07-01T23:59:59.000Z

69

Priorities in the design of chemical shops at coke plants  

SciTech Connect

Recent trends in the design of chemical equipment at coke plants are described, through the lens of experience at Giprokoks. The main priorities were to improve the removal of impurities from coke oven gas; to improve equipment design on the basis of new materials; to reduce reagent consumption; to reduce the materials and energy consumed in the construction of new equipment; and to minimize impacts on the environment and worker health. Some technological equipment is briefly characterized.

V.I. Rudyka; Y.E. Zingerman; V.V. Grabko; L.A. Kazak [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

70

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

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

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

71

Method and apparatus for selective removal of carbon monoxide  

DOE Patents (OSTI)

There is provided a method and apparatus for treatment of a hydrogen-rich gas to reduce the carbon monoxide content thereof by reacting the carbon monoxide in the gas with an amount of oxygen sufficient to oxidize at least a portion of the carbon monoxide in the presence of a catalyst in a desired temperature range without substantial reaction of hydrogen. The catalyst is an iridium-based catalyst dispersed on, and supported on, a carrier. In the presence of the catalyst, carbon monoxide in a hydrogen-rich feed gas is selectively oxidized such that a product stream is produced with a very low carbon monoxide content.

Borup, Rodney L. (East Rochester, NY); Skala, Glenn W. (Churchville, NY); Brundage, Mark A. (Pittsford, NY); LaBarge, William J. (Bay City, MI)

2000-01-01T23:59:59.000Z

72

Apparatus and method for removing solvent from carbon dioxide in resin recycling system  

SciTech Connect

A two-step resin recycling system and method solvent that produces essentially contaminant-free synthetic resin material. The system and method includes one or more solvent wash vessels to expose resin particles to a solvent, the solvent contacting the resin particles in the one or more solvent wash vessels to substantially remove contaminants on the resin particles. A separator is provided to separate the solvent from the resin particles after removal from the one or more solvent wash vessels. The resin particles are next exposed to carbon dioxide in a closed loop carbon dioxide system. The closed loop system includes a carbon dioxide vessel where the carbon dioxide is exposed to the resin, substantially removing any residual solvent remaining on the resin particles after separation. A separation vessel is also provided to separate the solvent from the solvent laden carbon dioxide. Both the carbon dioxide and the solvent are reused after separation in the separation vessel.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2009-01-06T23:59:59.000Z

73

Coking and gasification process  

DOE Patents (OSTI)

An improved coking process for normally solid carbonaceous materials wherein the yield of liquid product from the coker is increased by adding ammonia or an ammonia precursor to the coker. The invention is particularly useful in a process wherein coal liquefaction bottoms are coked to produce both a liquid and a gaseous product. Broadly, ammonia or an ammonia precursor is added to the coker ranging from about 1 to about 60 weight percent based on normally solid carbonaceous material and is preferably added in an amount from about 2 to about 15 weight percent.

Billimoria, Rustom M. (Houston, TX); Tao, Frank F. (Baytown, TX)

1986-01-01T23:59:59.000Z

74

Cyclic process for producing methane from carbon monoxide with heat removal  

DOE Patents (OSTI)

Carbon monoxide-containing gas streams are converted to methane by a cyclic, essentially two-step process in which said carbon monoxide is disproportionated to form carbon dioxide and active surface carbon deposited on the surface of a catalyst, and said carbon is reacted with steam to form product methane and by-product carbon dioxide. The exothermic heat of reaction generated in each step is effectively removed during each complete cycle so as to avoid a build up of heat from cycle-to-cycle, with particularly advantageous techniques being employed for fixed bed, tubular and fluidized bed reactor operations.

Frost, Albert C. (Congers, NY); Yang, Chang-lee (Spring Valley, NY)

1982-01-01T23:59:59.000Z

75

Intelligent control aeration and external carbon addition for improving nitrogen removal  

Science Conference Proceedings (OSTI)

Fuzzy logic can in several ways be applied to improve the control of the activated sludge system. In this paper, fuzzy logic based control strategies for external carbon flow in the anoxic zone and dissolved oxygen (DO) concentration in the aerobic zone ... Keywords: Energy saving, External carbon addition, Fuzzy control, Nitrogen removal, Predenitrification process

M. Yong; P. Yong-zhen; W. Xiao-lian; W. Shu-ying

2006-06-01T23:59:59.000Z

76

Fundamentals of Delayed Coking Joint Industry Project  

SciTech Connect

Delayed coking evolved steadily over the early to mid 1900s to enable refiners to convert high boiling, residual petroleum fractions to light products such as gasoline. Pound for pound, coking is the most energy intensive of any operation in a modern refinery. Large amounts of energy are required to heat the thick, poor-quality petroleum residuum to the 900 to 950 degrees F required to crack the heavy hydrocarbon molecules into lighter, more valuable products. One common misconception of delayed coking is that the product coke is a disadvantage. Although coke is a low valued (near zero economic value) byproduct, compared to transportation fuels, there is a significant worldwide trade and demand for coke as it is an economical fuel. Coke production has increased steadily over the last ten years, with further increases forecast for the foreseeable future. Current domestic production is near 111,000 tons per day. A major driving force behind this increase is the steady decline in crude quality available to refiners. Crude slates are expected to grow heavier with higher sulfur contents while environmental restrictions are expected to significantly reduce the demand for high-sulfur residual fuel oil. Light sweet crudes will continue to be available and in even greater demand than they are today. Refiners will be faced with the choice of purchasing light sweet crudes at a premium price, or adding bottom of the barrel upgrading capability, through additional new investments, to reduce the production of high-sulfur residual fuel oil and increase the production of low-sulfur distillate fuels. A second disadvantage is that liquid products from cokers frequently are unstable, i.e., they rapidly form gum and sediments. Because of intermediate investment and operating costs, delayed coking has increased in popularity among refiners worldwide. Based on the 2000 Worldwide Refining Survey published in the Oil and Gas, the delayed coking capacity for 101 refineries around the world is 2,937,439 barrels/calendar day. These cokers produce 154,607 tons of coke per day and delayed coking accounts for 88% of the world capacity. The delayed coking charge capacity in the United States is 1,787,860 b/cd. Despite its wide commercial use, only relatively few contractors and refiners are truly knowledgeable in delayed-coking design, so that this process carries with it a ''black art'' connotation. Until recently, the expected yield from cokers was determined by a simple laboratory test on the feedstock. As a result of Tulsa University's prior related research, a process model was developed that with additional work could be used to optimize existing delayed cokers over a wide range of potential feedstocks and operating conditions. The objectives of this research program are to: utilize the current micro, batch and pilot unit facilities at The University of Tulsa to enhance the understanding of the coking process; conduct additional micro and pilot unit tests with new and in-house resids and recycles to make current optimization models more robust; conduct focused kinetic experiments to enhance the furnace tube model and to enhance liquid production while minimizing sulfur in the products; conduct detailed foaming studies to optimize the process and minimize process upsets; quantify the parameters that affect coke morphology; and to utilize the knowledge gained from the experimental and modeling studies to enhance the computer programs developed in the previous JIP for optimization of the coking process. These refined computer models will then be tested against refinery data provided by the member companies. Novel concepts will also be explored for hydrogen sulfide removal of furnace gases as well as gas injection studies to reduce over-cracking. The following deliverables are scheduled from the two projects of the three-year JIP: (1) A novel method for enhancing liquid yields from delayed cokers and data that provide insight as to the optimum temperature to remove hydrogen sulfide from furnace gases. (2) An understanding of what causes foaming in c

Michael Volk Jr; Keith Wisecarver

2005-10-01T23:59:59.000Z

77

Summing up of discussion on improvement trends in coke-oven gas purification flowsheets  

SciTech Connect

Reference is made to a previously published article that included flowsheets for purification of coke-oven gas. It is concluded that the flowsheets for a process using arsenic-soda and vacuum-carbonate methods of sulfur removal in which the gas is cooled to 303-308/sup 0/K are seriously in error. Schemes involving minor refrigeration, sulfur removal by the circulating ammonia method and ammonia recovery as ammonia liquor are seen as promising but in need of further improvement. One scheme discussed (the VUKhIN scheme) involves ammonia recovery by the circulating phosphate method and sulfur removal by the circulating ammonia method is seen as a replacement for the minor refrigeration method. Since liquid ammonia consumption in agriculture is continually increasing, schemes that result in production of liquid ammonia rather than ammonia liquor should be seriously considered.

Zemblevskii, K.K.

1983-01-01T23:59:59.000Z

78

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

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

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

79

Coke | OpenEI  

Open Energy Info (EERE)

18 18 Varnish cache server Browse Upload data GDR 429 Throttled (bot load) Error 429 Throttled (bot load) Throttled (bot load) Guru Meditation: XID: 2142278418 Varnish cache server Coke Dataset Summary Description UK National coal (and solid fuels and gases derived from processing coal) are published in Chapter 2 (Solid Fuels and Derived Gases) of the Digest of UK Energy Statistics (DUKES). Included here are the datasets for commodity balances (1998 - 2009); supply and consumption (2005 - 2009) of coal and other fuels (e.g. coke oven gas, blast furnace gas, benzole and tars, etc). Chapter 2 of the report is available: http://www.decc.gov.uk/assets/decc/Statistics/publications/dukes/308-dukes-2010-ch2.pdf Source UK Department of Energy and Climate Change (DECC)

80

Design and construction of coke battery 1A at Radlin coke plant, Poland  

Science Conference Proceedings (OSTI)

In the design and construction of coke battery 1A at Radlin coke plant (Poland), coking of rammed coke with a stationary system was employed for the first time. The coke batteries are grouped in blocks. Safety railings are provided on the coke and machine sides of the maintenance areas.

A.M. Kravchenko; D.P. Yarmoshik; V.B. Kamenyuka; G.E. Kos'kova; N.I. Shkol'naya; V.V. Derevich; A.S. Grankin [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

Influence of Coke Calcining Parameters on Petroleum Coke ... - TMS  

Science Conference Proceedings (OSTI)

Jan 1, 1985 ... TMS Student Member price: 0.00. Product In Stock. Description All physical and chemical properties of petroleum coke are determined by three ...

82

An Experimental Study of Chemical Oxygen Demand Removal from ...  

Science Conference Proceedings (OSTI)

The experimental results showed that the refractory organics in coking wastewater can be effectively removed by this process, and COD removal efficiency was ...

83

Integration of stripping of fines slurry in a coking and gasification process  

DOE Patents (OSTI)

In an integrated fluid coking and gasification process wherein a stream of fluidized solids is passed from a fluidized bed coking zone to a second fluidized bed and wherein entrained solid fines are recovered by a wet scrubbing process and wherein the resulting solids-liquid slurry is stripped to remove acidic gases, the stripped vapors of the stripping zone are sent to the gas cleanup stage of the gasification product gas. The improved stripping integration is particularly useful in the combination coal liquefaction process, fluid coking of bottoms of the coal liquefaction zone and gasification of the product coke.

DeGeorge, Charles W. (Chester, NJ)

1980-01-01T23:59:59.000Z

84

Coke from coal and petroleum  

DOE Patents (OSTI)

A carbonaceous coke is manufactured by the delayed coking of a slurry mixture of from about 10 to about 30 weight percent of caking or non-caking coal and the remainder a petroleum resid blended at below 50.degree. C.

Wynne, Jr., Francis E. (Allison Park, PA); Lopez, Jaime (Pittsburgh, PA); Zaborowsky, Edward J. (Harwick, PA)

1981-01-01T23:59:59.000Z

85

Converting Petroleum Coke to Electricity  

E-Print Network (OSTI)

Changes in oil refining technology and economics are driving refiners to utilize thermal processes to maximize the conversion of heavy crude oil components to clean products. Since the primary unit operation to accomplish this objective is the coking unit, more cokers are being built, and existing cokers are being operated to maximum capacity utilization. SRI recently completed an assignment for a refiner interested in converting the by-product fluid coke from his unit to electricity. This paper presents the operating history of US based plants converting petroleum coke to electricity, and presents generic economics for the conversion process utilizing three primary technologies available: conventional pulverized coke combustion, atmospheric fluidized bed combustion, and coke gasification combined cycle power production.

Pavone, A.

1992-04-01T23:59:59.000Z

86

Georgia Refinery Marketable Petroleum Coke Production Capacity ...  

U.S. Energy Information Administration (EIA)

Georgia Refinery Marketable Petroleum Coke Production Capacity as of January 1 (Barrels per Stream Day)

87

Minnesota Refinery Marketable Petroleum Coke Production ...  

U.S. Energy Information Administration (EIA)

Minnesota Refinery Marketable Petroleum Coke Production Capacity as of January 1 (Barrels per Stream Day)

88

Coping with the Decline in Coke Quality – Using Onsite Blending ...  

Science Conference Proceedings (OSTI)

... coke (CPC), the blending of non-traditional cokes (NTAC's) has increased. ... Prebaked Anode from Coal - Utilization of Coal Extract as a Coke Feedstock-.

89

New coke-sorting system at OAO Koks  

SciTech Connect

A new coke-sorting system has been introduced at OAO Koks. It differs from the existing system in that it has no bunkers for all-purpose coke but only bunkers for commercial coke. In using this system with coke from battery 4, the crushing of the coke on conveyer belts, at roller screens, and in the commercial-coke bunkers is studied. After installing braking elements in the coke path, their effectiveness in reducing coke disintegration and improving coke screening is investigated. The granulometric composition and strength of the commercial coke from coke battery 3, with the new coke-sorting system, is evaluated.

B.Kh. Bulaevskii; V.S. Shved; Yu.V. Kalimin; S.D. Filippov [OAO Koks, Kemerovo (Russian Federation)

2009-05-15T23:59:59.000Z

90

Experimental study of elastoplastic mechanical properties of coke drum materials.  

E-Print Network (OSTI)

??Coke drums are vertical pressure vessels used in the delayed coking process in petroleum refineries. Significant temperature variation during the delayed coking process causes the… (more)

Chen, Jie

2010-01-01T23:59:59.000Z

91

Estimating Coke and Pepsi's Price and Advertising Strategies  

E-Print Network (OSTI)

Strategy Distributions for Coke (First Quarter 1977) a)Paper No. 789 ESTIMATING COKE AND PEPSI'S PRICE ADVERTISINGEconomics July, 1998 Estimating Coke and Pepsi’s Price and

Golan, Amos; Karp, Larry S.; Perloff, Jeffrey M.

1998-01-01T23:59:59.000Z

92

Prediction of Calcined Coke Bulk Density - Programmaster.org  

Science Conference Proceedings (OSTI)

Due to changing green coke quality, a reliable forecast of the calcined coke VBD from small green coke samples is required. The VBD can be predicted from ...

93

The use of carbonate lixiviants to remove uranium from uranium-contaminated soils  

SciTech Connect

The objective of this research was to design an extraction media and procedure that would selectively remove uranium without adversely affecting the soils` physicochemical characteristics or generating secondary waste forms difficult to manage or dispose of. Investigations centered around determining the best lixivant and how the various factors such as pH, time, and temperature influenced extraction efficiency. Other factors investigated included the influence of attrition scrubbing, the effect of oxidants and reductants and the recycling of lixiviants. Experimental data obtained at the bench- and pilot-scale levels indicated 80 to 95% of the uranium could be removed from the uranium-contaminated soils by using a carbonate lixiviant. The best treatment was three successive extractions with 0.25 M carbonate-bicarbonate (in presence of KMnO{sub 4} as an oxidant) at 40 C followed with two water rinses.

Francis, C.W.; Lee, S.Y.; Wilson, J.H. [Oak Ridge National Lab., TN (United States); Timpson, M.E.; Elless, M.P. [Oak Ridge Inst. for Science and Education, TN (United States)

1997-08-01T23:59:59.000Z

94

Coke gasification costs, economics, and commercial applications  

Science Conference Proceedings (OSTI)

The disposition of petroleum coke remains a problem for modern high conversion refineries. Market uncertainty and the price for coke can prevent the implementation of otherwise attractive projects. The commercially proven Texaco Gasification Process remains an excellent option for clean, cost effective coke disposition as demonstrated by the new coke gasification units coming on-line and under design. Previous papers, have discussed the coke market and general economics of coke gasification. This paper updates the current market situation and economics, and provide more details on cost and performance based on recent studies for commercial plants.

Jahnke, F.C.; Falsetti, J.S.; Wilson, R.F. [Texaco, Inc., White Plains, NY (United States)

1996-12-01T23:59:59.000Z

95

U.S. Imports of Petroleum Coke Marketable (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

Marketable Petroleum Coke Supply and Disposition; Petroleum Coke Imports from All Countries; U.S. Imports from All Countries ...

96

Evaluation of fly ash from co-combustion of coal and petroleum coke for use in concrete  

Science Conference Proceedings (OSTI)

An investigation of fly ash (FA) produced from various blends of coal and petroleum coke (pet coke) fired at Belledune Generating Station, New Brunswick, Canada, was conducted to establish its performance relative to FA derived from coal-only combustion and its compliance with CSA A3000. The FA samples were beneficiated by an electrostatic separation process to produce samples for testing with a range of loss-on-ignition (LOI) values. The results of these studies indicate that the combustion of pet coke results in very little inorganic residue (for example, typically less than 0.5% ash) and the main impact on FA resulting from the co-combustion of coal and up to 25% pet coke is an increase in the unburned carbon content and LOI values. The testing of FA after beneficiation indicates that FA produced from fuels with up to 25% pet coke performs as good as FA produced from the same coal without pet coke.

Scott, A.N.; Thomas, M.D.A.

2007-01-15T23:59:59.000Z

97

Advanced Green Petroleum Coke Calcination In Electrothermal ...  

Science Conference Proceedings (OSTI)

Symposium, Fluidization Technologies for the Mineral, Materials, and Energy Industries. Presentation Title, Advanced Green Petroleum Coke Calcination In ...

98

Cryogenic fractionator gas as stripping gas of fines slurry in a coking and gasification process  

DOE Patents (OSTI)

In an integrated coking and gasification process wherein a stream of fluidized solids is passed from a fluidized bed coking zone to a second fluidized bed and wherein entrained solid fines are recovered by a scrubbing process and wherein the resulting solids-liquid slurry is stripped with a stripping gas to remove acidic gases, at least a portion of the stripping gas comprises a gas comprising hydrogen, nitrogen and methane separated from the coker products.

DeGeorge, Charles W. (Chester, NJ)

1981-01-01T23:59:59.000Z

99

Trends in the automation of coke production  

SciTech Connect

Up-to-date mathematical methods, such as correlation analysis and expert systems, are employed in creating a model of the coking process. Automatic coking-control systems developed by Giprokoks rule out human error. At an existing coke battery, after introducing automatic control, the heating-gas consumption is reduced by {>=}5%.

R.I. Rudyka; Y.E. Zingerman; K.G. Lavrov [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

100

Removal of RDX and HMX from an artificial groundwater by granular activated carbon  

E-Print Network (OSTI)

Granular activated carbon (GAC) adsorption was efficient at removing high explosive contaminants such as Hexahydro-1,3,5-trinitro-1,3,5-tririne (RDX) and Octahydro-1,3,5,7-tetrritro-1,3,5,7-tetruocine (HMX) from an artificial groundwater (AGW). A completely mixed batch reactor (CMBR) system was selected for all rate and isotherm experiments. A number of rate and isotherm experiments were conducted to measure performance in the removal of RDX and HMX using GAC depending on dissolved oxygen, natural organic matter (NOM) preloading and GAC pretreatment. The investigation of competitive adsorption of RDX and Cr(VI) on GAC was conducted. In addition, IAST model predictions were made for RDX and HMX bisolute isotherms. When oxygen was excluded in the experimental system, there was enhancement in the removal of RDX from AGW using Fe[] pretreated GAC. However, in spite of this enhancement, it was still lower than the level of removal using virgin GAC as discussed below. According to the screening experiment results, dissolved Fe[]alone could not chemically reduce RDX. Despite expectations to the contrary based on the screening results, there was indeed some increase in the removal of RDX by Fe[] pretreated GAC under anaerobic conditions. It was suspected that in regard to the removal of RDX using GAC, there may have been chemical reactions occurring between RDX and the chemically reduced GAC surface under anaerobic conditions. Overall, the sorption capacity of GAC for RDX and HMX decreased as preloaded humid acid concentration increased. GAC procreated with a strong reluctant such as Fe[] or dithionite did not result in the enhancement of RDX removal from AGW compared with isotherms of virgin GAC under both aerobic and anaerobic conditions. Experimental values showed that for RDX, the single-solute isotherm data, bisolute isotherm data in the presence of Cr(VI) exhibited similar results. This suggests that the presence of Cr(VI) had negligible effect on RDX removal by GAC, indicating that competitive effects between RDX and Cr(VI) were minimal. Also, Cr(VI) removal was not significantly affected by the presence of RDX. IAST model predicted that the presence of HMX would reduce the adsorption of RDX compared to the single-solute isotherm of RDX. In the same manner, similar effects were obtained for HMX.

Im, Jeong Ran

1999-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

Clean Production of Coke from Carbonaceous Fines  

Science Conference Proceedings (OSTI)

In order to produce steel (a necessary commodity in developed nations) using conventional technologies, you must have metallurgical coke. Current coke-making technology pyrolyzes high-quality coking coals in a slot oven, but prime coking coals are becoming more expensive and slot ovens are being shut-down because of age and environmental problems. The United States typically imports about 4 million tons of coke per year, but because of a world-wide coke scarcity, metallurgical coke costs have risen from about $77 per tonne to more than $225. This coke shortage is a long-term challenge driving up the price of steel and is forcing steel makers to search for alternatives. Combustion Resources (CR) has developed a technology to produce metallurgical coke from alternative feedstocks in an environmentally clean manner. The purpose of the current project was to refine material and process requirements in order to achieve improved economic benefits and to expand upon prior work on the proposed technology through successful prototype testing of coke products. The ultimate objective of this project is commercialization of the proposed technology. During this project period, CR developed coke from over thirty different formulations that meet the strength and reactivity requirements for use as metallurgical coke. The technology has been termed CR Clean Coke because it utilizes waste materials as feedstocks and is produced in a continuous process where pollutant emissions can be significantly reduced compared to current practice. The proposed feed material and operating costs for a CR Clean Coke plant are significantly less than conventional coke plants. Even the capital costs for the proposed coke plant are about half that of current plants. The remaining barrier for CR Clean Coke to overcome prior to commercialization is full-scale testing in a blast furnace. These tests will require a significant quantity of product (tens of thousands of tons) necessitating the construction of a demonstration facility. Talks are currently underway with potential partners and investors to build a demonstration facility that will generate enough coke for meaningful blast furnace evaluation tests. If the testing is successful, CR Clean Coke could potentially eliminate the need for the United States to import any coke, effectively decreasing US Steel industry dependence on foreign nations and reducing the price of domestic steel.

Craig N. Eatough

2004-11-16T23:59:59.000Z

102

Passive CO{sub 2} removal using a carbon fiber composite molecular sieve  

SciTech Connect

Manufacture and characterization of a carbon fiber composite molecular sieve (CFCMS), and its efficacy as a CO{sub 2} gas adsorbent are reported. The CFCMS consists of an isotropic pitch derived carbon fiber and a phenolic resin derived carbon binder. Activation (selective gasification) of the CFCMS creates microporosity in the carbon fibers, yielding high micropore volumes (>0.5 cm{sup 3}/g) and BET surface areas (>1000 m{sup 2}/g). Moreover, the CFCMS material is a rigid, strong, monolith with an open structure that allows the free-flow of fluids through the material. This combination of properties provides an adsorbent material that has several distinct advantages over granular adsorbents in gas separation systems such as pressure swing adsorption (PSA) units. The results of our initial evaluations of the CO{sub 2} adsorption capacity and kinetics of CFCMS are reported. The room temperature CO{sub 2} adsorption capacity of CFCMS is >120 mg of CO{sub 2} per g of CFCMS. A proposed project is described that targets the development, over a three-year period, of a demonstration separation system based on CFCMS for the removal of CO{sub 2} from a flue gas slip stream at a coal-fired power plant. The proposed program would be conducted jointly with industrial and utility partners.

Burchell, T.D.; Judkins, R.R.

1995-12-01T23:59:59.000Z

103

Solution-reactor-produced-{sup 99}Mo using activated carbon to remove {sup 131}I  

SciTech Connect

This research explores the idea of producing {sup 99}Mo in a solution reactor. The Solution High Energy Burst Assembly (SHEBA), located at the Los Alamos Critical Assembly Facility, was used to facilitate this study. The goal of this study was to build on work previously completed and to investigate a possible mode of radioactive contaminant removal prior to a {sup 99}Mo extraction process. Prior experiments, performed using SHEBA and a single-step sorption process, showed a significant amount of {sup 131}I present along with the {sup 99}Mo on the alumina that was used to isolate the {sup 99}Mo. A high concentration of {sup 131}I and/or other contaminants present in a sample prohibits the Food and Drug Administration from approving an extraction of that nature for radiopharmaceutical use. However, if it were possible to remove the {sup 131}I and other contaminants prior to a {sup 99}Mo extraction, a simple column extraction process might be feasible. Activated charcoal was used to try to filter the {sup 131}I contaminant from an irradiated fuel solution. Gamma spectroscopy confirmed that the activated carbon trapped a significant amount of the {sup 131}I, as well as notable amounts of {sup 133}Xe, {sup 105}Rb, and {sup 140}Ba. Most importantly, the carbon traps a diminutive amount of {sup 99}Mo.

Kitten, S.; Cappiello, C. [Los Alamos National Lab., NM (United States)

1998-09-01T23:59:59.000Z

104

Thermal removal of mercury in spent powdered activated carbon from TOXECON process  

SciTech Connect

This research developed and demonstrated a technology to liberate Hg adsorbed onto powdered activated carbon (PAC) by the TOXECON process using pilot-scale high temperature air slide (HTAS) and bench-scale thermogravimetric analyzer (TGA). The HTAS removed 65, 83, and 92% of Hg captured with PAC when ran at 900{sup o}F, 1,000{sup o}F, and 1,200 {sup o}F, respectively, while the TGA removed 46 and 100% of Hg at 800 {sup o}F and 900{sup o}F, respectively. However, addition of CuO-Fe{sub 2}O{sub 3} mixture and CuCl catalysts enhanced Hg removal and PAC regeneration at lower temperatures. CuO-Fe{sub 2}O{sub 3} mixture performed better than CuCl in PAC regeneration. Scanning electron microscopy images and energy dispersive X-ray analysis show no change in PAC particle aggregation or chemical composition. Thermally treated sorbents had higher surface area and pore volume than the untreated samples indicating regeneration. The optimum temperature for PAC regeneration in the HTAS was 1,000{sup o}F. At this temperature, the regenerated sorbent had sufficient adsorption capacity similar to its virgin counterpart at 33.9% loss on ignition. Consequently, the regenerated PAC may be recycled back into the system by blending it with virgin PAC.

Okwadha, G.D.O.; Li, J.; Ramme, B.; Kollakowsky, D.; Michaud, D. [University of Wisconsin, Milwaukee, WI (United States)

2009-10-15T23:59:59.000Z

105

Coke gasification: the influence and behavior of inherent catalytic mineral matter  

Science Conference Proceedings (OSTI)

Gasification of coke contributes to its degradation in the blast furnace. In this study, the effect of gasification on the inherent catalytic minerals in cokes and their reciprocal influence on gasification are investigated. The catalytic mineral phases identified in the cokes used in this study were metallic iron, iron sulfides, and iron oxides. Metallic iron and pyrrhotite were rapidly oxidized during gasification to iron oxide. The catalysts had a strong influence on the apparent rates at the initial stages of reaction. As gasification proceeds, their effect on the reaction rate diminishes as a result of reducing the surface contact between catalyst and carbon matrix because of carbon consumption around the catalyst particles; with extended burnout the reactivity of the coke becomes increasingly dependent on surface area. The reaction rate in the initial stages was also influenced by the particle size of the catalytic minerals; for a given catalytic iron level, the cokes whose catalytic minerals were more finely dispersed had a higher apparent reaction rate than cokes containing larger catalytic particles. Iron, sodium, and potassium in the amorphous phase did not appear to affect the reaction rate. 40 refs., 16 figs., 6 tabs.

Mihaela Grigore; Richard Sakurovs; David French; Veena Sahajwalla [Commonwealth Scientific and Industrial Research Organisation (CSIRO), Bangor, NSW (Australia)

2009-04-15T23:59:59.000Z

106

Selecting the optimum coke pushing sequence  

SciTech Connect

The sequence of pushing coke ovens is one of the most important aspects of battery operation. The sequence must satisfy a number of technical and process conditions: (1) achieve maximum heating-wall life by avoiding destructive expansion pressure in freshly charged ovens and during pushing of the finished coke; (2) ensure uniform brickwork temperature and prevent overheating by compensating for the high thermal flux in freshly charged ovens due to accumulated heat in adjacent ovens that are in the second half of the coking cycle; (3) ensure the most favorable working conditions and safety for operating personnel; (4) provide additional opportunities for repair personnel to perform various types of work, such as replacing coke-machine rails, without interrupting coal production; (5) perform the maximum number of coke-machine operations simultaneously: pushing, charging, and cleaning doors, frames, and standpipe elbows; and (6) reduce electricity consumption by minimizing idle travel of coke machines.

V.T. Krivoshein; A.V. Makarov [ZAO Trest Koksokhimmontazh (Russian Federation)

2007-01-15T23:59:59.000Z

107

Coke oven gas desulphurization by the Carl Still process  

SciTech Connect

The Steubenville East Coke Plant need a desulfurization process that would desulfurize an eventual 95 million standard cubic feet per day of coke oven gas from an inlet of 450 gr/DSCF to an outlet of 45 gr/DSCF of hydrogen sulfide. The Dravo/Still plant process was selected, due to the use of ammonia which was available in the gas, as the absorbing agent. It was also a proven process. Dravo/Still also was capable of building a sulfuric acid plant. The desulfurization efficiency of the plant has consistently provided an average final gas sulfur loading below the guaranteed 45 gr/DSCF. This removal efficiency has enabled production of an average of 4615 tons per day of 66/sup 0/Be acid. Also SO/sub 2/ to SO/sub 3/ conversion has averaged 98%. 3 figures. (DP)

Knight, R.E.

1981-01-01T23:59:59.000Z

108

Electro-catalytic oxidation device for removing carbon from a fuel reformate  

SciTech Connect

An electro-catalytic oxidation device (ECOD) for the removal of contaminates, preferably carbonaceous materials, from an influent comprising an ECOD anode, an ECOD cathode, and an ECOD electrolyte. The ECOD anode is at a temperature whereby the contaminate collects on the surface of the ECOD anode as a buildup. The ECOD anode is electrically connected to the ECOD cathode, which consumes the buildup producing electricity and carbon dioxide. The ECOD anode is porous and chemically active to the electro-catalytic oxidation of the contaminate. The ECOD cathode is exposed to oxygen, and made of a material which promotes the electro-chemical reduction of oxygen to oxidized ions. The ECOD electrolyte is non-permeable to gas, electrically insulating and a conductor to oxidized. The ECOD anode is connected to the fuel reformer and the fuel cell. The ECOD electrolyte is between and in ionic contact with the ECOD anode and the ECOD cathode.

Liu, Di-Jia (Naperville, IL)

2010-02-23T23:59:59.000Z

109

Effect of thermal treatment on coke reactivity and catalytic iron mineralogy  

SciTech Connect

Iron minerals in coke can catalyze its gasification and may affect coke behavior in the blast furnace. The catalytic behavior of iron depends largely upon the nature of the iron-bearing minerals. To determine the mineralogical changes that iron could undergo in the blast furnace, cokes made from three coals containing iron present in different mineral forms (clays, carbonates, and pyrite) were examined. All coke samples were heat-treated in a horizontal furnace at 1373, 1573, and 1773 K and then gasified with CO{sub 2} at 1173 K in a fixed bed reactor (FBR). Coke mineralogy was characterized using quantitative X-ray diffraction (XRD) analysis of coke mineral matter prepared by low-temperature ashing (LTA) and field emission scanning electron microscopy combined with energy dispersive X-ray analysis (FESEM/EDS). The mineralogy of the three cokes was most notably distinguished by differing proportions of iron-bearing phases. During heat treatment and subsequent gasification, iron-containing minerals transformed to a range of minerals but predominantly iron-silicides and iron oxides, the relative amounts of which varied with heat treatment temperature and gasification conditions. The relationship between initial apparent reaction rate and the amount of catalytic iron minerals - pyrrhotite, metallic iron, and iron oxides - was linear and independent of heat treatment temperature at total catalyst levels below 1 wt %. The study showed that the coke reactivity decreased with increasing temperature of heat treatment due to decreased levels of catalytic iron minerals (largely due to formation of iron silicides) as well as increased ordering of the carbon structure. The study also showed that the importance of catalytic mineral matter in determining reactivity declines as gasification proceeds. 37 refs., 13 figs., 7 tabs.

Byong-chul Kim; Sushil Gupta; David French; Richard Sakurovs; Veena Sahajwalla [University of New South Wales, Sydney, NSW (Australia). Centre for Sustainable Materials Research and Technology

2009-07-15T23:59:59.000Z

110

Entrained Flow Gasification of Oil Sand Coke.  

E-Print Network (OSTI)

??The effect of blending woody biomass material with fluid coke and coal on the co-pyrolysis process was investigated in an entrained flow gasifier. The SEM… (more)

Vejahati, Farshid

2012-01-01T23:59:59.000Z

111

Characterization of Packing Ability of Coke Particles  

Science Conference Proceedings (OSTI)

VBD is conventionally used in anode industry to determine the required amount of pitch and fine coke. VBD may be achieved by dense particles while they do ...

112

Estimating Coke and Pepsi's price and advertising strategies  

E-Print Network (OSTI)

Working Paper No. 789 ESTIMATING COKE AND PEPSI’ PRICE S ANDand Advertising Strategies: Coke and Pepsi) by Amos Golan,Revised, March 1999 Estimating Coke and Pepsi’s Price and

Golan, Amos; Karp, Larry; Perloff, Jeffrey M.

1999-01-01T23:59:59.000Z

113

Evolution of Anode Grade Calcined Coke - Programmaster.org  

Science Conference Proceedings (OSTI)

The term "anode grade coke" has been used as a broad definition to describe delayed coke with a sponge structure containing relatively low levels of trace ...

114

New designs in the reconstruction of coke-sorting systems  

Science Conference Proceedings (OSTI)

In recent Giprokoks designs for the reconstruction of coke-sorting systems, high-productivity vibrational-inertial screens have been employed. This permits single-stage screening and reduction in capital and especially operating expenditures, without loss of coke quality. In two-stage screening, >80 mm coke (for foundry needs) is additionally separated, with significant improvement in quality of the metallurgical coke (25-80 mm). New designs for the reconstruction of coke-sorting systems employ mechanical treatment of the coke outside the furnace, which offers new scope for stabilization of coke quality and permits considerable improvement in mechanical strength and granulometric composition of the coke by mechanical crushing.

A.S. Larin; V.V. Demenko; V.L. Voitanik [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

115

Effect of Coke Particle Size on Sinter Quality  

Science Conference Proceedings (OSTI)

Abstract Scope, The effect of different Coke particle size on sinter quality has been investigated. Eight different coke particle sizes were chosen and sinter ...

116

Improving the Precision and Productivity of Green Coke VCM Analysis  

Science Conference Proceedings (OSTI)

Green cokes with high VCM (>12%) are more difficult to calcine and result in a higher porosity and lower bulk density in calcined coke. The paper will review ...

117

Observations on the Coke Air Reactivity Test - Programmaster.org  

Science Conference Proceedings (OSTI)

Coke air reactivities are strongly dependent on coke calcination levels and it is possible to drive air reactivities lower by increasing calcining temperatures.

118

Crystalline structure transformation of carbon anodes during gasification  

Science Conference Proceedings (OSTI)

The crystalline structure transformation of five carbon anodes during gasification in air and carbon dioxide was studied using quantitative X-ray diffraction (XRD) analysis and high-resolution transmission electron microscopy (HRTEM). XRD analysis and HRTEM observations confirmed that anodes have a highly ordered graphitic structure. The examination of partially gasified samples indicated that crystalline structure transformation occurred in two stages during gasification. The first stage involved the consumption of disorganized carbon matter in the initial 15% conversion. Oxygen was found to be more reactive toward disorganized carbon at this stage of the gasification process compared to carbon dioxide. Following this stage, as more carbon was consumed, especially with the removal of smaller crystallites, it was found that the crystalline structure became more ordered with increasing conversion levels. This is due to the merging of neighboring crystallites, required to maintain the minimum energy configuration. In addition, the interaction between the pitch and the coke components was found to be strongly linked to the initial coke structure. 'Stress graphitization' occurred at the pitch-coke interface, which helps to enhance the structural development of the anodes. 26 refs., 9 figs., 3 tabs.

Kien N. Tran; Adam J. Berkovich; Alan Tomsett; Suresh K. Bhatia [University of Queensland, St. Lucia, Qld. (Australia). Division of Chemical Engineering

2008-05-15T23:59:59.000Z

119

Forest Restoration Carbon Analysis of Baseline Carbon Emissions and Removal in Tropical Rainforest at La Selva Central, Peru  

DOE Green Energy (OSTI)

Conversion of tropical forest to agricultural land and pasture has reduced forest extent and the provision of ecosystem services, including watershed protection, biodiversity conservation, and carbon sequestration. Forest conservation and reforestation can restore those ecosystem services. We have assessed forest species patterns, quantified deforestation and reforestation rates, and projected future baseline carbon emissions and removal in Amazon tropical rainforest at La Selva Central, Peru. The research area is a 4800 km{sup 2} buffer zone around the Parque Nacional Yanachaga-Chemillen, Bosque de Proteccion San Matias-San Carlos, and the Reserva Comunal Yanesha. A planned project for the period 2006-2035 would conserve 4000 ha of forest in a proposed 7000 ha Area de Conservacion Municipale de Chontabamba and establish 5600 ha of natural regeneration and 1400 ha of native species plantations, laid out in fajas de enriquecimiento (contour plantings), to reforest 7000 ha of agricultural land. Forest inventories of seven sites covering 22.6 ha in primary forest and 17 sites covering 16.5 ha in secondary forest measured 17,073 trees of diameter {ge} 10 cm. The 24 sites host trees of 512 species, 267 genera, and 69 families. We could not identify the family of 7% of the trees or the scientific species of 21% of the trees. Species richness is 346 in primary forest and 257 in the secondary forest. In primary forest, 90% of aboveground biomass resides in old-growth species. Conversely, in secondary forest, 66% of aboveground biomass rests in successional species. The density of trees of diameter {ge} 10 cm is 366 trees ha{sup -1} in primary forest and 533 trees ha{sup -1} in secondary forest, although the average diameter is 24 {+-} 15 cm in primary forest and 17 {+-} 8 cm in secondary forest. Using Amazon forest biomass equations and wood densities for 117 species, aboveground biomass is 240 {+-} 30 t ha{sup -1} in the primary sites and 90 {+-} 10 t ha{sup -1} in the secondary sites. Aboveground carbon density is 120 {+-} 15 t ha{sup -1} in primary forest and 40 {+-} 5 t ha{sup -1} in secondary forest. Forest stands in the secondary forest sites range in age from 10 to 42 y. Growth in biomass (t ha{sup -1}) as a function of time (y) follows the relation: biomass = 4.09-0.017 age{sup 2} (p < 0.001). Aboveground biomass and forest species richness are positively correlated (r{sup 2} = 0.59, p < 0.001). Analyses of Landsat data show that the land cover of the 3700 km{sup 2} of non-cloud areas in 1999 was: closed forest 78%; open forest 12%, low vegetation cover 4%, sparse vegetation cover 6%. Deforestation from 1987 to 1999 claimed a net 200 km{sup 2} of forest, proceeding at a rate of 0.005 y{sup -1}. Of those areas of closed forest in 1987, only 89% remained closed forest in 1999. Consequently, closed forests experienced disruption in the time period at double the rate of net deforestation. The three protected areas experienced negligible deforestation or slight reforestation. Based on 1987 forest cover, 26,000 ha are eligible for forest carbon trading under the Clean Development Mechanism, established by the Kyoto Protocol to the United Nations Framework Convention on Climate Change. Principal components analysis showed that distance to nonforest was the factor that best explained observed patterns of deforestation while distance to forest best explained observed patterns of reforestation, more significant than elevation, distance to rivers, distance to roads, slope, and distance to towns of population > 400. Aboveground carbon in live vegetation in the project area decreased from 35 million {+-} 4 million t in 1987 to 34 million {+-} 4 million t in 1999. Projected aboveground carbon in live vegetation would fall to 33 million {+-} 4 million t in 2006, 32 million {+-} 4 million t in 2011, and 29 million {+-} 3 million t in 2035. Projected net deforestation in the research area would total 13,000 {+-} 3000 ha in the period 1999-2011, proceeding at a rate of 0.003 {+-} 0.0007 y{sup -1}, and would total 33,000 {+-} 7000

Patrick Gonzalez; Benjamin Kroll; Carlos R. Vargas

2006-01-10T23:59:59.000Z

120

Exhibitor: R&D CARBON LTD.  

Science Conference Proceedings (OSTI)

R&D Carbon Ltd. serves the petroleum coke, pitch and aluminum industries. Research and Development: Basic resarch is carried out to better understand ...

Note: This page contains sample records for the topic "remove carbon coke" 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

Colorado Refinery Marketable Petroleum Coke Production Capacity as ...  

U.S. Energy Information Administration (EIA)

Colorado Refinery Marketable Petroleum Coke Production Capacity as of January 1 (Barrels per Stream Day)

122

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

SciTech Connect

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

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

2011-10-11T23:59:59.000Z

123

Petroleum Coke: A Viable Fuel for Cogeneration  

E-Print Network (OSTI)

Petroleum coke is a by-product of the coking process which upgrades (converts) low-valued residual oils into higher-valued transportation, heating and industrial fuels. Pace forecasts that by the year 2000 petroleum coke production will increase from 36 million to 47 million short tons/year. Because the crude pool will continue to become more sour and refiners treat the coker as the "garbage can" the quality of the petroleum cokes will generally degrade- contain higher sulfur and trace metal levels. The U.S. produces nearly 70% of the total and is expected to maintain this share. Domestic markets consumed less than half of the U.S. production; 80% of the high sulfur fuel grade production from the Gulf coast is exported to Japan or Europe. Increasing environmental concerns could disrupt historic markets and threaten coker operations. This would create opportunities for alternate end-uses such as cogeneration projects. The Pace Consultants Inc. continuously monitors and reports on the petroleum coke industry-production and markets-in its multi-client publication The Pace Petroleum Coke Ouarterly. The information presented in this paper is based on this involvement and Pace's experience in single and multi client consulting activities related to the petroleum refining and petroleum coke industries. The purpose is to provide a review of the existing world petroleum coke industry with particular emphasis on the U.S. production and markets. Forecasted production levels and critical factors which could alter the historic market disposition of petroleum coke are addressed.

Dymond, R. E.

1992-04-01T23:59:59.000Z

124

Method for the wet quenching of coke  

SciTech Connect

A method and apparatus for the wet quenching of coke is disclosed wherein hot coke is sprayed from above with quenching water, the steam generated by the heat of the coke is condensed by a spray of condensation water from the top of the quenching tower, and the hot condensate-water mixture is collected at the bottom of the quenching tower and recirculated to the top of the tower where it is sprayed between quenching operations to be cooled by a counterflowing stream of air. The cooled condensate water mixture is suitable for reuse as the condensation spray water.

Blase, M.; Flockenhaus, C.; Wagener, D.

1982-03-30T23:59:59.000Z

125

Heteroatom incorporated coke for electrochemical cell electrode  

DOE Patents (OSTI)

This invention relates to an electrode for a coke/alkali metal electrochemical cell comprising: (a) calcined coke particles: (i) that contain at least 0.5 weight percent of nitrogen heteroatoms and at least 1.0 weight percent sulfur heteroatoms, and (ii) that have an average particle size from 2 microns to 40 microns with essentially no particles being greater than 50 microns. (b) a binder This invention also relates to a coke/alkali metal electrochemical cell comprising: (a) an electrode as described above, (b) a non-aqueous electrolytic solution comprising an organic aprotic solvent and an electrically conductive salt, and (c) a counterelectrode.

Lewis, Irwin Charles (Strongsville, OH); Greinke, Ronald Alfred (Medina, OH)

1997-01-01T23:59:59.000Z

126

Heteroatom incorporated coke for electrochemical cell electrode  

DOE Patents (OSTI)

This invention relates to an electrode for a coke/alkali metal electrochemical cell comprising: (a) calcined coke particles: (1) that contain at least 0.5 weight percent of nitrogen heteroatoms and at least 1.0 weight percent sulfur heteroatoms, and (2) that have an average particle size from 2 microns to 40 microns with essentially no particles being greater than 50 microns and (b) a binder. This invention also relates to a coke/alkali metal electrochemical cell comprising: (a) an electrode as described above, (b) a non-aqueous electrolytic solution comprising an organic aprotic solvent and an electrically conductive salt, and (c) a counterelectrode. 5 figs.

Lewis, I.C.; Greinke, R.A.

1997-06-17T23:59:59.000Z

127

Spatial variation of coke quality in the non-recovery beehive coke ovens.  

E-Print Network (OSTI)

??More than 50% of hot metal production worldwide takes place in blast furnaces. Coke is the most expensive raw material in the blast furnace. It… (more)

Segers, Magrieta

2006-01-01T23:59:59.000Z

128

Réactivité de l'anode et désulfuration : effet du niveau de calcination du coke.  

E-Print Network (OSTI)

??Les propriétés du coke et la performance des anodes sont affectées par le niveau de calcination du coke. Une densité de coke (VBD) élevée implique… (more)

Bergeron-Lagacé, Charles-Luc

2012-01-01T23:59:59.000Z

129

Mozambique becomes a major coking coal exporter?  

SciTech Connect

In addition to its potential role as a major international supplier of coking coal, Mozambique will also become a major source of power generation for southern Africa. 3 figs.

Ruffini, A.

2008-06-15T23:59:59.000Z

130

New and revised standards for coke production  

SciTech Connect

The need for new and revised standards for coke production in Ukraine and Russia is outlined. Such standards should address improvements in plant operation, working conditions, environmental protection, energy conservation, fire and explosion safety, and economic indices.

G.A. Kotsyuba; M.I. Alpatov; Y.G. Shapoval [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

131

Characterization of tuyere-level core-drill coke samples from blast furnace operation  

SciTech Connect

A suite of tuyere-level coke samples have been withdrawn from a working blast furnace during coal injection, using the core-drilling technique. The samples have been characterized by size exclusion chromatography (SEC), Fourier transform Raman spectroscopy (FT-RS), and X-ray powder diffraction (XRD) spectroscopy. The 1-methyl-2-pyrrolidinone (NMP) extracts of the cokes sampled from the 'bosh', the rear of the 'bird's nest', and the 'dead man' zones were found by SEC to contain heavy soot-like materials (ca. 10{sup 7}-10{sup 8} apparent mass units). In contrast, NMP extracts of cokes taken from the raceway and the front of the 'bird's nest' only contained a small amount of material of relatively lower apparent molecular mass (up to ca. 10{sup 5} u). Since the feed coke contained no materials extractable by the present method, the soot-like materials are thought to have formed during the reactions of volatile matter released from the injectant coal, probably via dehydrogenation and repolymerization of the tars. The Raman spectra of the NMP-extracted core-drilled coke samples showed variations reflecting their temperature histories. Area ratios of D-band to G-band decreased as the exposure temperature increased, while intensity ratios of D to G band and those of 2D to G bands increased with temperature. The graphitic (G), defect (D), and random (R) fractions of the carbon structure of the cokes were also derived from the Raman spectra. The R fractions decreased with increasing temperature, whereas G fractions increased, while the D fractions showed a more complex variation with temperature. These data appear to give clues regarding the graphitization mechanism of tuyere-level cokes in the blast furnace. 41 refs., 9 figs., 6 tabs.

S. Dong; N. Paterson; S.G. Kazarian; D.R. Dugwell; R. Kandiyoti [Imperial College London, London (United Kingdom). Department of Chemical Engineering

2007-12-15T23:59:59.000Z

132

Coke Gasification - A Solution to Excess Coke Capacity and High Energy Costs  

E-Print Network (OSTI)

United States crude slate is becoming heavier and generally higher in sulfur. At the same time demand of distillate products is increasing. Refiners are reworking their plans to include resid conversion via coking and approximately 230,000 BPD of new coking capacity is either under construction or announced. Even if 50 percent of the coke produced is exported, there will be an excess capacity of coke selling at less than $30/ton depending upon the sulfur content. This coke can be gasified effectively to produce medium-Btu (300 Btu/scf) gas which, in turn, can fuel the refinery furnaces to replace natural gas. Coke gasification should prove economical with natural gas price decontrol and the average price projected to rise to over $14.0 per million Btu in 1990. The paper will discuss three gasifiers - Gesellschaft fur Kohle-Technologie Gmbh (GKT), Texaco and Westinghouse which may be used for the production of medium-Btu gas from coke. The design parameters, which for coke gasification may be different from coal gasification because of the difference in physical and chemical characteristics of coke and coal, will be evaluated. Conceptual design will be performed based upon normal fuel requirements of about 20 billion Btu per day for a typical 50,000 BPD refinery. Adaptability of coke derived gas to refinery fuel systems will be discussed in terms of flame temperatures, flue gas volumes, derating and required furnace modifications. Estimates of capital and operating costs will be obtained to calculate the gas cost using the new tax laws. Finally, the GKT gasifier will be compared to the developing Texaco and Westinghouse gasifiers to assess the effect of second generation gasifiers on the economics of coke gasification.

Patel, S. S.

1982-01-01T23:59:59.000Z

133

Giprokoks proposals for improvement in air quality at coke battery 1A of Radlin coke plant  

SciTech Connect

Coke battery 1A, which uses rammed batch, has gone into production at Radlin coke plant (Poland), on the basis of Giprokoks designs. Up-to-date dust-trapping methods are used for the first time within the aspiration systems in the coal-preparation shop and in improving dust collection within the production buildings.

T.F. Trembach; A.G. Klimenko [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

134

Rapid Changes in Soil Carbon and Structural Properties Due to Stover Removal from No-Till Corn Plots  

SciTech Connect

Harvesting corn (Zea mays L.) stover for producing ethanol may be beneficial to palliate the dependence on fossil fuels and reduce CO2 emissions to the atmosphere, but stover harvesting may deplete soil organic carbon (SOC) and degrade soil structure. We investigated the impacts of variable rates of stover removal from no-till (NT) continuous corn systems on SOC and soil structural properties after 1 year of stover removal in three soils in Ohio: Rayne silt loam (fine-loamy, mixed, active, mesic Typic Hapludults) at Coshocton, Hoytville clay loam (fine, illitic, mesic Mollic Epiaqualfs) at Hoytville, and Celina silt loam (fine, mixed, active, mesic Aquic Hapludalfs) at South Charleston. This study also assessed relationships between SOC and soil structural properties as affected by stover management. Six stover treatments that consisted of removing 100, 75, 50, 25, and 0, and adding 100% of corn stover corresponding to 0 (T0), 1.25 (T1.25), 2.50 (T2.5), 3.75 (T3.75), 5.00 (T5), and 10.00 (T10) Mg haj1 of stover, respectively, were studied for their total SOC concentration, bulk density (>b), aggregate stability, and tensile strength (TS) of aggregates. Effects of stover removal on soil properties were rapid and significant in the 0- to 5-cm depth, although the magnitude of changes differed among soils after only 1 year of stover removal. The SOC concentration declined with increase in removal rates in silt loams but not in clay loam soils. It decreased by 39% at Coshocton and 30% at Charleston within 1 year of complete stover removal. At the same sites, macroaggregates contained 10% to 45% more SOC than microaggregates. Stover removal reduced 94.75-mm macroaggregates and increased microaggregates (P G 0.01). Mean weight diameter (MWD) and TS of aggregates in soils without stover (T0) were 1.7 and 3.3 times lower than those in soils with normal stover treatments (T5) across sites. The SOC concentration was negatively correlated with >b and positively with MWD and LogTS. Stover removal at rates as low as 1.25 Mg haj1 reduced SOC and degraded soil structure even within 1 year, but further monitoring is needed to establish threshold levels of stover removal in relation to changes in soil quality.

Blanco-Canqui, H; Lal, Rattan; Post, W M.; Izaurralde, R Cesar C.; Owens, L B.

2006-06-01T23:59:59.000Z

135

The carbon footprint analysis of wastewater treatment plants and nitrous oxide emissions from full-scale biological nitrogen removal processes in Spain  

E-Print Network (OSTI)

This thesis presents a general model for the carbon footprint analysis of advanced wastewater treatment plants (WWTPs) with biological nitrogen removal processes, using a life cycle assessment (LCA) approach. Literature ...

Xu, Xin, S.M. Massachusetts Institute of Technology

2013-01-01T23:59:59.000Z

136

CO2 Removal from Gas Streams Using a Carbon Fiber Composite Molecular  

E-Print Network (OSTI)

A novel adsorbent carbon monolith has been developed at Oak Ridge National Laboratory. The monolith is fabricated from isotropic-pitch-derived carbon fibers and powdered phenolic resin via a slurry molding process. The resultant green-form is dried, cured, and carbonized to convert the phenolic resin to carbon, and then activated to develop a connected network of micropores within the carbon fibers and resin-derived carbon binder. The monolith is also macroporous, exhibiting large (>50 µm) pores between the fibers. The resultant open structure allows the free flow of fluids through the monoliths such that gases can reach the micropores where they may be selectively adsorbed. This novel adsorbent has been named a “carbon fiber composite molecular sieve” (CFCMS). Several separations have been demonstrated such as the separation of hydrogen from experimental gas mixtures containing H2 and H2S or H2 and CO2; the separation of CO2 from CH4; the separation of CO2 from air; and the separation of CO2, CO, H2S, and H2O from a variety of proprietary gas mixtures. The CFCMS is being investigated as a CO2 separation and capture device in carbon mitigation strategies for natural gas processing, fuel cells, and gas turbines. The monolithic material is rigid and strong, resistant to attrition and dusting, and because of its continuous carbon skeletal structure, electrically conductive. An adsorbed gas may be quickly and efficiently desorbed by the passage of an electric current, thereby allowing for a low-energy, electrical-swing separation system. It is possible to regenerate the carbon monoliths in the absence of a temperature increase, potentially reducing swing cycle times and improving separation efficiency. The structure and properties of the adsorbent CFCMS monoliths are reported. Some information on the experimental apparatus is provided. Breakthrough plots and performance data for CO2 separation and capture are presented, and the electrical swing adsorption process is discussed

Roddie R. Judkins; Timothy D. Burchell

2001-01-01T23:59:59.000Z

137

Mechanical Properties of Submicrocrystalline 0.19%C Low Carbon ...  

Science Conference Proceedings (OSTI)

Mathematical Modeling of Coke Bed Gasification ... Mechanical Properties and Biocompatibility in-vitro and in-vivo of Plasma Sprayed Carbon Nanotube ...

138

NETL: News Release - Worldwide Carbon Capture and Storage Projects...  

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

of slagging gasifiers, where a carbon-based feedstock (such as coal, petroleum, coke, andor biomass) is converted at high temperatures in an oxygen short atmosphere into...

139

Development of coke strength after reaction (CSR) at Dofasco  

Science Conference Proceedings (OSTI)

In order to prevent coke degradation without detrimentally affecting blast furnace service life, Dofasco initiated a project to improve coke strength after reaction. The results of the program and Dofasco's prediction model are presented. 9 refs., 12 figs., 9 tabs.

T.W. Todoschuk; J.P. Price; J.F. Gransden

2004-03-01T23:59:59.000Z

140

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

By incorporating amines inside clay containing quaternary ammonium salts (organoclay) minerals, this invention has created a way to prepare sorbents that capture carbon dioxide (CO2) from low temperature and low pressure gas streams. In this process, ...

Note: This page contains sample records for the topic "remove carbon coke" 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

Carbonized material adsorbents for the removal of mercury from aqueous solutions  

SciTech Connect

Although wood has essentially been excluded as a starting material for the production of granular activated carbon because of the poor strength and friability of the products, powdered wood based activated carbons are still being used in water treatment and other liquid phase applications. However, the capability of powdered wood-based charcoal which in itself porous has not been fully known. Few studies have been conducted in harnessing its potential for adsorption purposes especially in water treatment. This study was conducted to investigate the possibility of using wood based carbonized materials from Sugi (Cryptomeria japonica D. Don) as adsorption materials in aqueous solutions of heavy metals like mercury, zinc, lead, cadmium and arsenic. However, of all the heavy metals investigated, mercury is considered to be the most toxic so this paper describes only the adsorption ability of the carbonized materials in adsorbing this metal from aqueous solutions of different concentrations.

Ishihara, S.; Pulido, L.L. [Kyoto Univ. (Japan); Kajimoto, T. [Wakayama Industrial Technology Center (Japan)

1996-12-31T23:59:59.000Z

142

Desulphurization of coke oven gas by the Stretford Process  

SciTech Connect

The Stretford process is probably the most effective means available for removing hydrogen sulphide from gas streams. For streams which do not contain hydrogen cyanide or excessive oxygen it should be nearly ideal. However, the large volume of waste liquor generated by fixation of hydrogen cyanide has prevented its widespread adoption for coke oven gas treatment. Investigations of various proposals for treating the waste liquor indicate that the only practicable way of dealing with it is by reductive incineration. Although attempts to apply the Peabody-Holmes reductive incineration process have been disappointing, significant progress in overcoming some of its deficiencies has been made. The Zimpro wet oxidation process will provide a convenient method of treating the HCN scrubber effluent at No. 1 Plant. However, it will not treat the sodium based liquor from the Stretford plant. Its application to Stretford waste treatment is limited to situations where ammonium liquors and ammonium sulphate recovery facilities are available. Commissioning of this plant has been delayed while a defect in the air compressor supplied for the plant is being remedied. When the problem of liquid effluent disposal has been overcome, and if reagent chemicals continue to be available at reasonable prices, the Stretford process will be a good choice for coke oven gas desulphurization. 8 figures.

Plenderleith, J.

1981-01-01T23:59:59.000Z

143

Innovative coke oven gas cleaning system for retrofit applications  

Science Conference Proceedings (OSTI)

Bethlehem Steel Corporation (BSC), in conjunction with the Department of Energy (DOE) is conducting a Clean Coal Technology (CCT) project at its Sparrows Point, Maryland Coke Oven Plant. This project combines several existing technologies into an integrated system for removing impurities from Coke Oven Gas (COG) to make it an acceptable fuel. DOE is providing cost-sharing under a Cooperative Agreement with BSC. This Cooperative Agreement requires BSC to develop and conduct an Environmental Monitoring Plan (EMP) for the Clean Coal Technology project and to report the status of the EMP on a quarterly basis. This report is the third quarterly status report of the EMP. It covers the Environmental Monitoring Plan activities for the full year of 1991 from January 1, 1991 through December 31, 1991, including the forth quarter. See Sections 2, 3 and 4 for status reports of the Project Installation and Commissioning, the Environmental Monitoring activities and the Compliance Monitoring results for the period. Section 5 contains a list of Compliance Reports submitted to regulatory agencies during the period. The EMP describes in detail the environmental monitoring activities to be performed during the project execution. The purpose of the EMP is to: (1) document the extent of compliance of monitoring activities, i.e. those monitoring required to meet permit requirements, (2) confirm the specific impacts predicted in the National Environmental Policy Act documentation, and (3) establish an information base for the assessment of the environmental performance of the technology demonstrated by the project.

Not Available

1992-10-16T23:59:59.000Z

144

Recycling of rubber tires in electric arc furnace steelmaking: simultaneous combustion of metallurgical coke and rubber tyres blends  

Science Conference Proceedings (OSTI)

The present study investigates the effect of addition of waste rubber tires on the combustion behavior of its blends with coke for carbon injection in electric arc furnace steelmaking. Waste rubber tires were mixed in different proportions with metallurgical coke (MC) (10:90, 20:80, 30:70) for combustion and pyrolysis at 1473 K in a drop tube furnace (DTF) and thermogravimetric analyzer (TGA), respectively. Under experimental conditions most of the rubber blends indicated higher combustion efficiencies compared to those of the constituent coke. In the early stage of combustion the weight loss rate of the blends is much faster compared to that of the raw coke due to the higher volatile yield of rubber. The presence of rubber in the blends may have had an impact upon the structure during the release and combustion of their high volatile matter (VM) and hence increased char burnout. Measurements of micropore surface area and bulk density of the chars collected after combustion support the higher combustion efficiency of the blends in comparison to coke alone. The surface morphology of the 30% rubber blend revealed pores in the residual char that might be attributed to volatile evolution during high temperature reaction in oxygen atmosphere. Physical properties and VM appear to have a major effect upon the measured combustion efficiency of rubber blends. The study demonstrates that waste rubber tires can be successfully co-injected with metallurgical coke in electric arc furnace steelmaking process to provide additional energy from combustion. 44 refs., 11 figs., 2 tabs.

Magdalena Zaharia; Veena Sahajwalla; Byong-Chul Kim; Rita Khanna; N. Saha-Chaudhury; Paul O'Kane; Jonathan Dicker; Catherine Skidmore; David Knights [University of New South Wales, Sydney, NSW (Australia). School of Materials Science and Engineering

2009-05-15T23:59:59.000Z

145

Characterization of Petroleum Coke and Butts Used in Anode ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, Materials Science & Technology 2013. Symposium, Particulate Composites. Presentation Title, Characterization of Petroleum Coke ...

146

U.S. Refinery Thermal Cracking, Fluid Coking Downstream Charge ...  

U.S. Energy Information Administration (EIA)

U.S. Refinery Thermal Cracking, Fluid Coking Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

147

U.S. Refinery Marketable Petroleum Coke Production Capacity as ...  

U.S. Energy Information Administration (EIA)

U.S. Refinery Marketable Petroleum Coke Production Capacity as of January 1 (Barrels per Stream Day)

148

Effect of Coke particle size on sinter quality  

Science Conference Proceedings (OSTI)

Meeting, 2011 TMS Annual Meeting & Exhibition. Symposium, EMPMD Technical Division Student Poster Contest. Presentation Title, Effect of Coke particle size ...

149

Effect of Trace Elements on Anaerobic Digestion of Coking Wastewater  

Science Conference Proceedings (OSTI)

The pretreatment of coking wastewater using ASBR was conducted at 35? in this paper. The addition of trace elements to the anaerobic reactor has positive effect on the anaerobic treatment of coking wastewater, but too much or too little of it will ... Keywords: trace elements, anaerobic digestion, coking wastewater

Yu-ying Li; Bing Li

2009-10-01T23:59:59.000Z

150

Financial Analysis for Developing CDM Project in the Coke Plant  

Science Conference Proceedings (OSTI)

In the coke plant, the traditional coke wet quenching method is to be used to cool down the red hot coke and waste heat is released to the atmosphere in China. There are a lot of smog, particles, cyanide, sulphide and etc. mixtures within the waste heat. ... Keywords: CDQ technology, CO2 emission reductions, financial analysis, potential calculation, recycle sustainable development

Ma Xiuqin; Huang Chao; Wu Guoning

2009-05-01T23:59:59.000Z

151

Kansas refinery starts up coke gasification unit  

SciTech Connect

Texaco Refining and Marketing Inc. has started up a gasification unit at its El Dorado, Kan., refinery. The unit gasifies delayed coke and other refinery waste products. This is the first refinery to install a coke-fueled gasification unit for power generation. Start-up of the $80-million gasification-based power plant was completed in mid-June. The gasifier produces syngas which, along with natural gas, fuels a combustion turbine. The turbine produces virtually 100% of the refinery`s electricity needs and enough heat to generate 40% of its steam requirements.

Rhodes, A.K.

1996-08-05T23:59:59.000Z

152

Fundamentals of Delayed Coking Joint Industry Project  

Science Conference Proceedings (OSTI)

The coking test facilities include three reactors (or cokers) and ten utilities. Experiments were conducted using the micro-coker, pilot-coker, and stirred-batch coker. Gas products were analyzed using an on-line gas chromatograph. Liquid properties were analyzed in-house using simulated distillation (HP 5880a), high temperature gas chromatography (6890a), detailed hydrocarbon analysis, and ASTM fractionation. Coke analyses as well as feedstock analyses and some additional liquid analyses (including elemental analyses) were done off-site.

Volk Jr., Michael; Wisecarver, Keith D.; Sheppard, Charles M.

2003-02-07T23:59:59.000Z

153

Reducing dust emissions at OAO Alchevskkoks coke battery 10A  

Science Conference Proceedings (OSTI)

Coke battery 10A with rammed batch is under construction at OAO Alchevskkoks. The design documentation developed by Giprokoks includes measures for reducing dust emissions to the atmosphere. Aspiration systems with dry dust trapping are employed in the new components of coke battery 10A and in the existing coke-sorting equipment. Two-stage purification of dusty air in cyclones and bag filters is employed for the coke-sorting equipment. This system considerably reduces coke-dust emissions to the atmosphere.

T.F. Trembach; E.N. Lanina [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

154

Innovative coke oven gas cleaning system for retrofit applications. Volume 1, Public design report  

SciTech Connect

This Public Design Report provides, in a single document, available nonproprietary design -information for the ``Innovative Coke Oven Gas Cleaning System for Retrofit Applications`` Demonstration Project at Bethlehem Steel Corporation`s Sparrows Point, Maryland coke oven by-product facilities. This project demonstrates, for the first time in the United States, the feasibility of integrating four commercially available technologies (processes) for cleaning coke oven gas. The four technologies are: Secondary Gas Cooling, Hydrogen Sulfide and Ammonia Removal, Hydrogen Sulfide and Ammonia Recovery, and Ammonia Destruction and Sulfur Recovery. In addition to the design aspects, the history of the project and the role of the US Department of,Energy are briefly discussed. Actual plant capital and projected operating costs are also presented. An overview of the integration (retrofit) of the processes into the existing plant is presented and is followed by detailed non-proprietary descriptions of the four technologies and their overall effect on reducing the emissions of ammonia, sulfur, and other pollutants from coke oven gas. Narrative process descriptions, simplified process flow diagrams, input/output stream data, operating conditions, catalyst and chemical requirements, and utility requirements are given for each unit. Plant startup provisions, environmental considerations and control monitoring, and safety considerations are also addressed for each process.

Not Available

1994-05-24T23:59:59.000Z

155

Recycling of waste polymers in electric arc furnace steelmaking: slag/carbon and steel/carbon interactions.  

E-Print Network (OSTI)

??This project is focused on utilizing polymer/coke blends as carbon resource in EAF steelmaking process. In-depth investigations were carried out on slag/carbon and steel/carbon interactions… (more)

Kongkarat, Somyote

2011-01-01T23:59:59.000Z

156

Methanation of gas streams containing carbon monoxide and hydrogen  

DOE Patents (OSTI)

Carbon monoxide-containing gas streams having a relatively high concentration of hydrogen are pretreated so as to remove the hydrogen in a recoverable form for use in the second step of a cyclic, essentially two-step process for the production of methane. The thus-treated streams are then passed over a catalyst to deposit a surface layer of active surface carbon thereon essentially without the formation of inactive coke. This active carbon is reacted with said hydrogen removed from the feed gas stream to form methane. The utilization of the CO in the feed gas stream is appreciably increased, enhancing the overall process for the production of relatively pure, low-cost methane from CO-containing waste gas streams.

Frost, Albert C. (Congers, NY)

1983-01-01T23:59:59.000Z

157

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

158

Innovative coke oven gas cleaning system for retrofit applications. Environmental Monitoring program. Volume 1 - sampling progrom report. Baseline Sampling Program report  

Science Conference Proceedings (OSTI)

Bethlehem Steel Corporation (BSC), in conjunction with the Department of Energy (DOE) is conducting a Clean Coal Technology (CCT) project at its Sparrows Point, Maryland Coke Oven Plant. This innovative coke oven gas cleaning system combines several existing technologies into an integrated system for removing impurities from Coke Oven Gas (COG) to make it an acceptable fuel. DOE provided cost-sharing under a Cooperative Agreement with BSC. This Cooperative Agreement requires BSC to develop and conduct and Environmental Monitoring Plan for the Clean Coal Technology project and to report the status of the EMP on a quarterly basis. It also requires the preparation of a final report on the results of the Baseline Compliance and Supplemental Sampling Programs that are part of the EMP and which were conducted prior to the startup of the innovative coke oven gas cleaning system. This report is the Baseline Sampling Program report.

Stuart, L.M.

1994-05-27T23:59:59.000Z

159

REDUCING POWER PRODUCTION COSTS BY UTILIZING PETROLEUM COKE  

SciTech Connect

A Powder River Basin subbituminous coal from the North Antelope mine and a petroleum shot coke were received from Northern States Power Company (NSP) for testing the effects of parent fuel properties on coal-coke blend grindability and evaluating the utility of petroleum coke blending as a strategy for improving electrostatic precipitator (ESP) particulate collection efficiency. Petroleum cokes are generally harder than coals, as indicated by Hardgrove grindability tests. Therefore, the weaker coal component may concentrate in the finer size fractions during the pulverizing of coal-coke blends. The possibility of a coal-coke size fractionation effect is being investigated because it may adversely affect combustion performance. Although the blending of petroleum coke with coal may adversely affect combustion performance, it may enhance ESP particulate collection efficiency. Petroleum cokes contain much higher concentrations of V relative to coals. Consequently, coke blending can significantly increase the V content of fly ash resulting from coal-coke combustion. Pentavalent vanadium oxide (V{sub 2}O{sub 5}) is a known catalyst for transforming gaseous sulfur dioxide (SO{sub 2}[g]) to gaseous sulfur trioxide (SO{sub 3}[g]). The presence of SO{sub 3}(g) strongly affects fly ash resistivity and, thus, ESP performance.

NONE

1998-09-01T23:59:59.000Z

160

Table 16. U.S. Coke Exports  

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

U.S. Coke Exports U.S. Coke Exports (short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Table 16. U.S. Coke Exports (short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Year to Date Continent and Country of Destination April - June 2013 January - March 2013 April - June 2012 2013 2012 Percent Change North America Total 162,796 79,217 201,795 242,013 340,944 -29.0 Canada* 73,859 17,837 112,348 91,696 161,596 -43.3 Mexico 88,535 60,517 86,721 149,052 176,163 -15.4 Other** 402 863 2,726 1,265 3,185 -60.3 South America Total 223 217 591 440 1,158 -62.0 Other** 223 217 591 440 1,158 -62.0 Europe Total 48,972 59,197 - 108,169 6 NM Other** 347 11,743 - 12,090 - - United Kingdom 48,625 47,454 - 96,079 6 NM Asia Total 317 553 633 870 4,778

Note: This page contains sample records for the topic "remove carbon coke" 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

Table 21. U.S. Coke Imports  

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

U.S. Coke Imports U.S. Coke Imports (short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Table 21. U.S. Coke Imports (short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Year to Date Continent and Country of Origin April - June 2013 January - March 2013 April - June 2012 2013 2012 Percent Change North America Total 10,284 2,293 159,462 12,577 183,712 -93.2 Canada 3,009 2,293 159,462 5,302 183,712 -97.1 Panama 7,275 - - 7,275 - - South America Total 25,267 13,030 88,424 38,297 106,612 -64.1 Brazil - - 78,595 - 78,595 - Colombia 25,267 13,030 9,829 38,297 28,017 36.7 Europe Total 6,044 40,281 165,027 46,325 485,791 -90.5 Czech Republic - 170 - 170 - - Spain 363 - - 363 - - Ukraine 5,681 40,111 5,047 45,792 53,543 -14.5 United Kingdom

162

Removal of Mercury from SBW Vitrification Off-Gas by Activated Carbon  

SciTech Connect

Radioactive, acidic waste stored at the Idaho Nuclear Technology and Engineering Center (INTEC) have been previously converted into a dry, granular solid at the New Waste Calcining Facility (NWCF). As an alternative to calcination, direct vitrification of the waste, as well as the calcined solids in an Idaho Waste Vitrification Facility (IWVF) is being considered to prepare the waste for final disposal in a federal repository. The remaining waste to be processed is Sodium-Bearing Waste (SBW). Off-gas monitoring during NWCF operations have indicated that future mercury emissions may exceed the proposed Maximum Achievable Control Technology (MACT) limit of 130 ug/dscm (micrograms/dry standard cubic meter) @ 7% O2 for existing Hazardous Waste Combustors (HWC) if modifications are not made. Carbon monoxide and hydrocarbon emissions may also exceed the MACT limits. Off-gas models have predicted that mercury levels in the off-gas from SBW vitrification will exceed the proposed MACT limit of 45 ug/dscm @ 7% O2 for new HWCs. NO2/44% H2O.

Deldebbio, John Anthony; Watson, T. T.; Kirkham, Robert John

2001-09-01T23:59:59.000Z

163

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

164

Design and economics for low pressure delayed coking  

Science Conference Proceedings (OSTI)

The current refining trend is to run heavier crudes with a growing emphasis on bottom of the barrel resid upgrading. In general, a reduction in light crude availability and a corresponding increase in the price differential between light and heavy crudes makes the processing of heavier crudes highly attractive. US Department of Energy data indicate that between 1985 and 1989 the average API gravity of crude being processed in the US dropped from 32.46 to 32.14 degrees while the average sulfur content increased 0.15 wt%. As crudes get heavier and the demand for light, clean fuels increases, expanded resid upgrading capacity is rapidly becoming a necessity for most refiners. The coking process has existed since the early 1900's, and delayed coking is still favored as a relatively low cost resid upgrading option. Consistent with the objective of maximizing resid conversion, recent trends in delayed coking include maximizing liquid yields and reducing the production of petroleum coke by operating coke drums at lower pressures. Typically, the incremental liquid gained at lower pressures is worth significantly more than coke and can be further upgraded to lighter products. In addition, the driving force to minimize coke make has been accelerated by the worsening quality of crude oils. As vacuum resid feedstocks become heavier, contaminants in coke such as sulfur and metals are increased, making the coke less marketable. In the case of an existing coker which is capacity limited by coke make, a reduction in coke yield can be quite valuable. This paper discusses the design features and presents the economics associated with building a low pressure delayed coker with a 15 psig coke drum operating pressure versus a more conventional 25 psig design.

Bansal, B.B.; Moretta, J.C.; Gentry, A.R. (M.W. Kellogg Co., Houston, TX (United States))

1993-01-01T23:59:59.000Z

165

Vibrated Bulk Density (VBD) of Calcined Petroleum Coke and ...  

Science Conference Proceedings (OSTI)

Abstract Scope, Vibrated bulk density (VBD) is a quantitative measurement used in the aluminum industry to evaluate the density of calcined petroleum coke.

166

Vibrated Bulk Density (VBD) of Calcined Petroleum Coke and ...  

Science Conference Proceedings (OSTI)

Presentation Title, Vibrated Bulk Density (VBD) of Calcined Petroleum Coke and Implications of Changes in the ASTM Method D4292. Author(s), Bill Spencer, ...

167

Coking is a refinery process that produces 19% of finished ...  

U.S. Energy Information Administration (EIA)

Financial market analysis and financial data ... hydraulically cutting the coke using water. ... to a heater as a fluidized solid where some of it is ...

168

Determination of Coke Calcination Level and Anode Baking Level  

Science Conference Proceedings (OSTI)

Presentation Title, Determination of Coke Calcination Level and Anode Baking Level – Application and Reproducibility of Lc Based Methods. Author(s), Stein ...

169

Use of Coal Tar Pitch Coke for Producing Prebaked Electrodes  

Science Conference Proceedings (OSTI)

The study was conducted in order to (1) find an alternative material to petroleum coke due to its high cost and deteriorating properties, and (2) determine the ...

170

Modélisation thermomécanique d'un piédroit de four à coke.  

E-Print Network (OSTI)

??Inscrite dans le cadre du projet européen Coke Oven Operating Limits, cette thèse porte sur la modélisation thermomécanique d'un piédroit de cokerie. Le piédroit est… (more)

Landreau, Matthieu

2009-01-01T23:59:59.000Z

171

Discrete Element Method Applied to the Vibration Process of Coke ...  

Science Conference Proceedings (OSTI)

In the present work, effects of particle shape and size distribution on vibrated bulk density (VBD) of dry coke samples have been investigated. Discrete Element ...

172

Increasing Coke Impurities – Is this Really a Problem for Metal ...  

Science Conference Proceedings (OSTI)

Abstract Scope, Increases in the Vanadium and Nickel content of anode grade coke in recent years have predictably affected smelter metal quality. This has now ...

173

Prediction of Coke Quality in Ironmaking Process: A Data Mining Approach.  

E-Print Network (OSTI)

??Coke is an indispensable material in Ironmaking process by blast furnace. To provide good and constant quality coke for stable and efficient blast furance operation… (more)

Hsieh, Hsu-huang

2006-01-01T23:59:59.000Z

174

Fossil fuel derivatives with reduced carbon. Phase I final report  

Science Conference Proceedings (OSTI)

This project involves the simultaneous production of clean fossil fuel derivatives with reduced carbon and sulfur, along with value-added carbon nanofibers. This can be accomplished because the nanofiber production process removes carbon via a catalyzed pyrolysis reaction, which also has the effect of removing 99.9% of the sulfur, which is trapped in the nanofibers. The reaction is mildly endothermic, meaning that net energy production with real reductions in greenhouse emissions are possible. In Phase I research, the feasibility of generating clean fossil fuel derivatives with reduced carbon was demonstrated by the successful design, construction and operation of a facility capable of utilizing coal as well as natural gas as an inlet feedstock. In the case of coal, for example, reductions in CO{sub 2} emissions can be as much as 70% (normalized according to kilowatts produced), with the majority of carbon safely sequestered in the form of carbon nanofibers or coke. Both of these products are value-added commodities, indicating that low-emission coal fuel can be done at a profit rather than a loss as is the case with most clean-up schemes. The main results of this project were as follows: (1) It was shown that the nanofiber production process produces hydrogen as a byproduct. (2) The hydrogen, or hydrogen-rich hydrocarbon mixture can be consumed with net release of enthalpy. (3) The greenhouse gas emissions from both coal and natural gas are significantly reduced. Because coal consumption also creates coke, the carbon emission can be reduced by 75% per kilowatt-hour of power produced.

Kennel, E.B.; Zondlo, J.W.; Cessna, T.J.

1999-06-30T23:59:59.000Z

175

Method of washing hydrogen sulfide from coke oven gas by the ammonium sulfide method  

Science Conference Proceedings (OSTI)

An improved coke oven gas washing process for removing hydrogen sulfide is proposed wherein the coke oven gas is treated in a hydrogen sulfide scrubber by counterflow with an aqueous ammonia wash water. A stream of aqueous weak ammonia liquor is cooled and sprayed through nozzles in the mid-region of the hydrogen sulfide scrubber. A quantity of aqueous ammonia liquor, corresponding to the quantity which is sprayed through the said nozzles, is withdrawn from the hydrogen sulfide scrubber at a level below the nozzles and is introduced into the top of the said hydrogen sulfide scrubber. Ammonia vapor released at the nozzles has a higher partial pressure than the ammonia partial pressure of the coke oven gas in the region of the nozzle. The aqueous ammonia liquor from the deacidifier is the source of the cooled aqueous ammonia liquor which is introduced through the nozzles. A portion of the aqueous ammonia liquor from the deacidifier is introduced directly into the top of the hydrogen sulfide scrubber as a portion of the required aqueous ammonia wash water.

Ritter, H.

1985-05-21T23:59:59.000Z

176

Co-carbonization of two anthracites with a fat coal or two pitches  

SciTech Connect

The blends of two anthracite powders (YQ and JC) with a fat coal (C4) or a petroleum pitch (PP) or a coal tar pitch (CTP) in different proportions were co-carbonized at 3{sup o}C/min up to 1000{sup o}C in an experimental 1 kg coke oven. Coke yield, coke particulate size, coke micro-strength and coke cracking strength were measured respectively. Coke optical textures were watched under a microscope. The results show that as anthracite proportion increases, coke yields of all blends improve; > 0.8 mm lump coke yields of blends with CTP or PP decline slightly, blends with C4 drop heavily; coke microstrengths do not change sharply, and coke cracking strength of blends with C4 or PP decrease more than blends with CTP. C4 produces fine-grained mosaics, and two anthracites are mainly fusinite and fragments, PP is coarse-grained mosaics, and CTP is chiefly flow or domain textures. Independent optical textures were observed in cokes. There exist evident borders between the two contact optical textures which were produced by different components, and a few phenomena that domain or flow textures penetrating into fusinite appeared in the blends. It seems that CTP is the best adhesives for blending with anthracites for producing high quality cokes.

Shen, J.; Wang, Z.Z. [Taiyuan University of Technology, Taiyuan (China). College of Chemical Engineering & Technology

2006-04-15T23:59:59.000Z

177

Form EIA-5 Users Manual Quarterly Coal Consumption and Quality - Coke Plants  

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

5 5 Users Manual Quarterly Coal Consumption and Quality - Coke Plants Document Number: 001 Version: 2.0 June 2011 i June 2011 Document History Number Date Section Description 1 2 June 2011 June 2011 Document initiation Revised screen shots and remove external user references. Primary POC: Tejasvi Raghuveer Phone: (202) 586-8926 Email: Tejasvi.Raghuveer@eia.gov Document Changes/Maintenance POC: Primary POC: Tejasvi Raghuveer Phone: (202) 586-8926 Email: Tejasvi.Raghuveer@eia.gov Project References: Coal Internet Data Collection (CIDC) User's Manual, September 2007 ii June 2011 Content 1. General System Overview ................................................................................. 1

178

U.S. Exports to Saudi Arabia of Petroleum Coke (Thousand ...  

U.S. Energy Information Administration (EIA)

Petroleum Coke Exports by Destination; Saudi Arabia Exports of Crude Oil and Petroleum Products by Destination ...

179

U.S. Exports to South Africa of Petroleum Coke (Thousand ...  

U.S. Energy Information Administration (EIA)

Petroleum Coke Exports by Destination; South Africa Exports of Crude Oil and Petroleum Products by Destination ...

180

Coke profile and effect on methane/ethylene conversion process  

E-Print Network (OSTI)

The objective of this study was to investigate the coke profile with respect to time on stream and the change of product distribution due to catalyst deactivation. A fixed bed reactor was used to conduct this investigation. A series of runs were conducted using the Engelhard catalyst with fixed operating conditions. The only variable was the time on stream of each run. Six experiments were conducted starting with one hour time on stream up to six hours with an increment of one hour. In each experiment data on product flow rate, reactor temperature, and product distribution were collected. And at the end of each run, the amount of coke deposited on the catalyst was measured. Hydrogen concentration in the product distribution decreased as a function of time on stream. On the other hand, low and high end hydrocarbons increased with time on stream. The coke deposition kinetics for the catalyst at the process operating conditions can be estimated using Voorhies' empirical formula. The coke profile inside the reactor showed that the coke reaction follows a parallel mechanism to the main reaction. Ethylene was found to be the main coke precursor; however, the participation of methane in the coke reaction could not be neglected.

Al-Solami, Bandar

2002-01-01T23:59:59.000Z

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


181

Coke mineral transformations in the experimental blast furnace  

SciTech Connect

Blast furnace efficiency may be improved by optimizing coke reactivity. Some but not all forms of mineral matter in the coke modify its reactivity, but changes in mineral matter that occur within coke while in the blast furnace have not been fully quantified. To determine changes in mineral matter forms in the blast furnace, coke samples from a dissection study in the LKAB experimental blast furnace (EBF) were characterized using SEM/EDS analysis, EPMA (microprobe), and low-temperature ashing/quantitative XRD analysis. Variations in alkali concentration, particularly potassium, dominated the compositional changes. At high concentrations of potassium, the mineral matter was largely potassium-bearing but even more potassium was diffused throughout the coke and not associated with mineral matter. There was little difference in potassium concentration between the core and surface of the coke pieces, suggesting that potassium diffused rapidly through the whole coke. Iron, calcium, silicon, and aluminum concentrations were relatively constant in comparison, although the mineralogy of all elements changed significantly with changing temperature. 23 refs., 20 figs., 9 tabs.

Kelli Kazuberns; Sushil Gupta; Mihaela Grigore; David French; Richard Sakurovs; Mats Hallin; Bo Lindblom; Veena Sahajwalla [University of New South Wales, Sydney, NSW (Australia). Cooperative Research Centre for Coal in Sustainable Development (CCSD)

2008-09-15T23:59:59.000Z

182

Variation in coke properties within the blast-furnace shop  

SciTech Connect

In active production at OAO Magnitogorskii Metallurgicheskii Kombinat (MMK), samples of melt materials were taken during shutdown and during planned repairs at furnaces 1 and 8. In particular, coke was taken from the tuyere zone at different distances from the tuyere tip. The mass of the point samples was 2-15 kg, depending on the sampling zone. The material extracted from each zone underwent magnetic separation and screening by size class. The resulting coke sample was averaged out and divided into parts: one for determining the granulometric composition and mechanical strength; and the other for technical analysis and determination of the physicochemical properties of the coke.

E.N. Stepanov; I.I. Mel'nikov; V.P. Gridasov; A.A. Stepanova [OAO Magnitogorskii Metallurgicheskii Kombinat (MMK), Magnitogorsk, (Russian Federation)

2009-04-15T23:59:59.000Z

183

An example of alkalization of SiO{sub 2} in a blast furnace coke  

SciTech Connect

Scanning electron microscopy and an electron-microprobe analysis of a sample of blast furnace (BF) coke have revealed alkalization (5.64 wt % Na{sub 2}O + K{sub 2}O) and Al saturation (17.28 wt % Al{sub 2}O{sub 3}) of SiO{sub 2} by BF gases. The K/Na{sub at} value of 1.15 in the new phase (alteration zone) reflects close atomic proportions of the elements and suggests that the abilities to incorporate K and Na during the process are almost equal. This Al saturation and alkalization of SiO{sub 2} indicates an active role for Al along with alkali metals in BF gases. The average width of the altered area in the SiO{sub 2} grain is about 10 m, which suggests that SiO{sub 2} particles of that size can be transformed fully to the new phase, provided that at least one of their faces is open to an external pore (surface of the coke) or internal pore with circulating BF gases. The grains that exceed 10 {mu}m can only be partly altered, which means that smaller SiO{sub 2} grains can incorporate more alkali metals and Al (during their transformation to the Al and alkali-bearing phase) than a similar volume of SiO{sub 2} concentrated in larger grains. Thermodynamic calculations for 100 g{sub solid}/100 g{sub gas} and temperatures 800-1800{sup o}C have shown that the BF gases have very little or no effect on the alkalization of SiO{sub 2}. If the alteration process described in this paper proves to be a generalized phenomenon in blast furnace cokes, then the addition of fine-grained quartz to the surface of the coke before charging a BF can be useful for removing of some of the Al and alkali from the BF gases and reduce coke degradation by alkalis, or at least improve its properties until the temperature reaches approximately 2000{sup o}C. 22 refs., 5 figs., 1 tab.

S.S. Gornostayev; P.A. Tanskanen; E.-P. Heikkinen; O. Kerkkonen; J.J. Haerkki [University of Oulu, Oulu (Finland). Laboratory of Process Metallurgy

2007-09-15T23:59:59.000Z

184

Gulf Coast (PADD 3) Catalyst Petroleum Coke Consumed at ...  

U.S. Energy Information Administration (EIA)

Gulf Coast (PADD 3) Catalyst Petroleum Coke Consumed at Refineries (Thousand Barrels) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 ...

185

Comprehensive Effect of Coke Breeze and Limestone Particle Size ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

186

Table 38. Coal Stocks at Coke Plants by Census Division  

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

Coal Stocks at Coke Plants by Census Division Coal Stocks at Coke Plants by Census Division (thousand short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Table 38. Coal Stocks at Coke Plants by Census Division (thousand short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Census Division June 30, 2013 March 31, 2013 June 30, 2012 Percent Change (June 30) 2013 versus 2012 Middle Atlantic w w w w East North Central 1,313 1,177 1,326 -1.0 South Atlantic w w w w East South Central w w w w U.S. Total 2,500 2,207 2,295 8.9 w = Data withheld to avoid disclosure. Note: Total may not equal sum of components because of independent rounding. Source: U.S. Energy Information Administration (EIA), Form EIA-5, 'Quarterly Coal Consumption and Quality Report - Coke Plants.'

187

U.S. Ending Stocks of Petroleum Coke (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

U.S. Ending Stocks of Petroleum Coke (Thousand Barrels) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9; 1980's: 4,502: ...

188

U.S. Exports of Petroleum Coke (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

U.S. Exports of Petroleum Coke (Thousand Barrels) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9; 1980's: 50,292: ...

189

U.S. Petroleum Coke Consumed at Refineries (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

U.S. Petroleum Coke Consumed at Refineries (Thousand Barrels) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9; 1980's: ...

190

U.S. Exports of Petroleum Coke (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

U.S. Exports of Petroleum Coke (Thousand Barrels) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec; 1981: 2,754: 4,394: 3,722: 3,995: 5,211: ...

191

U.S. Petroleum Coke Stocks at Refineries (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

U.S. Petroleum Coke Stocks at Refineries (Thousand Barrels) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec; 1993: 10,747: 11,072: 11,444: ...

192

Nippon Coke and Engineering Sumitomo Corp JV | Open Energy Information  

Open Energy Info (EERE)

and Engineering Sumitomo Corp JV Jump to: navigation, search Name Nippon Coke and Engineering & Sumitomo Corp JV Place Tokyo, Japan Zip 135-6007 Product Japan-based natural...

193

PRODUCTION OF CARBON PRODUCTS USING A COAL EXTRACTION PROCESS  

Science Conference Proceedings (OSTI)

This Department of Energy National Energy Technology Laboratory sponsored project developed carbon products, using mildly hydrogenated solvents to extract the organic portion of coal to create synthetic pitches, cokes, carbon foam and carbon fibers. The focus of this effort was on development of lower cost solvents, milder hydrogenation conditions and improved yield in order to enable practical production of these products. This technology is needed because of the long-term decline in production of domestic feedstocks such as petroleum pitch and coal tar pitch. Currently, carbon products represents a market of roughly 5 million tons domestically, and 19 million tons worldwide. Carbon products are mainly derived from feedstocks such as petroleum pitch and coal tar pitch. The domestic supply of petroleum pitch is declining because of the rising price of liquid fuels, which has caused US refineries to maximize liquid fuel production. As a consequence, the long term trend has a decline in production of petroleum pitch over the past 20 years. The production of coal tar pitch, as in the case of petroleum pitch, has likewise declined significantly over the past two decades. Coal tar pitch is a byproduct of metallurgical grade coke (metcoke) production. In this industry, modern metcoke facilities are recycling coal tar as fuel in order to enhance energy efficiency and minimize environmental emissions. Metcoke production itself is dependent upon the production requirements for domestic steel. Hence, several metcoke ovens have been decommissioned over the past two decades and have not been replaced. As a consequence sources of coal tar are being taken off line and are not being replaced. The long-term trend is a reduction in coal tar pitch production. Thus import of feedstocks, mainly from Eastern Europe and China, is on the rise despite the relatively large transportation cost. To reverse this trend, a new process for producing carbon products is needed. The process must be economically competitive with current processes, and yet be environmentally friendly as well. The solvent extraction process developed uses mild hydrogenation of low cost oils to create powerful solvents that can dissolve the organic portion of coal. The insoluble portion, consisting mainly of mineral matter and fixed carbon, is removed via centrifugation or filtration, leaving a liquid solution of coal chemicals and solvent. This solution can be further refined via distillation to meet specifications for products such as synthetic pitches, cokes, carbon foam and fibers. The most economical process recycles 85% of the solvent, which itself is obtained as a low-cost byproduct from industrial processes such as coal tar or petroleum refining. Alternatively, processes have been developed that can recycle 100% of the solvent, avoiding any need for products derived from petroleum or coal tar.

Dady Dadyburjor; Philip R. Biedler; Chong Chen; L. Mitchell Clendenin; Manoj Katakdaunde; Elliot B. Kennel; Nathan D. King; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

2004-08-31T23:59:59.000Z

194

Evaluation of active transport membranes for carbon dioxide removal from hydrogen containing streams. Approved final topical report  

SciTech Connect

Air Products and Chemicals, Inc. is developing a new class of gas separation membranes called Active Transport Membranes (ATM). ATMs are unique in that they permeate acid gas components, via a reactive pathway, to the low pressure side of the membrane while retaining lighter, non-reactive gases at near feed pressure. This feature is intuitively attractive for hydrogen and synthesis gas processes where CO{sub 2} removal is desired and the hydrogen or synthesis gas product is to be used at elevated pressure. This report provides an overview of the technology status and reports on preliminary, order of magnitude assessments of ATMs for three applications requiring CO{sub 2} removal from gas streams containing hydrogen. The end uses evaluated are: CO{sub 2} removal in the COREX{reg_sign} Steel making process--upgrading export gas for a Direct Reducing Iron (DRI) process; CO{sub 2} removal for onboard hydrogen gas generators for mobile fuel cell applications; Bulk CO{sub 2} removal from hydrogen plant synthesis gas--a plant de-bottlenecking analysis for ammonia production. For each application, an overview of the process concept, rough equipment sizing and techno-economic evaluation against competing technologies is provided. Brief descriptions of US and world market conditions are also included.

Cook, P.J.; Laciak, D.V.; Pez, G.P.; Quinn, R.

1995-11-01T23:59:59.000Z

195

Prediction of metallurgical coke strength from the petrographic composition of coal blends  

Science Conference Proceedings (OSTI)

Turkey, especially Zonguldak on the West Coast of Black Sea region, has large reserves of bituminous coal that can be used either directly or in blends with other coals for metallurgical coke production. It is possible to predict the coking properties of these coals by petrographic analysis. In this study, semi- and non-coking coals were blended with coking bituminous coals in varying proportions and an estimation was made as to their stability factors through petrographic techniques. It was established that semi- and non-coking bituminous coals could be used in the production of metallurgical coke.

Sutcu, H.; Toroglu, I.; Piskin, S. [Zonguldak Karaelmas University, Zonguldak (Turkey)

2009-07-01T23:59:59.000Z

196

Hydrodesulfurization of Fluid Catalytic Cracking Decant Oils for the Production of Low-sulfur Needle Coke Feedstocks.  

E-Print Network (OSTI)

??Needle coke, produced by the delayed coking of fluid catalytic cracking decant oils, is the primary filler used in the production of graphite electrodes. The… (more)

Wincek, Ronald

2013-01-01T23:59:59.000Z

197

Integrated Removal of NOx with Carbon Monoxide as Reductant, and Capture of Mercury in a Low Temperature Selective Catalytic and Adsorptive Reactor  

SciTech Connect

Coal will likely continue to be a dominant component of power generation in the foreseeable future. This project addresses the issue of environmental compliance for two important pollutants: NO{sub x} and mercury. Integration of emission control units is in principle possible through a Low Temperature Selective Catalytic and Adsorptive Reactor (LTSCAR) in which NO{sub x} removal is achieved in a traditional SCR mode but at low temperature, and, uniquely, using carbon monoxide as a reductant. The capture of mercury is integrated into the same process unit. Such an arrangement would reduce mercury removal costs significantly, and provide improved control for the ultimate disposal of mercury. The work completed in this project demonstrates that the use of CO as a reductant in LTSCR is technically feasible using supported manganese oxide catalysts, that the simultaneous warm-gas capture of elemental and oxidized mercury is technically feasible using both nanostructured chelating adsorbents and ceria-titania-based materials, and that integrated removal of mercury and NO{sub x} is technically feasible using ceria-titania-based materials.

Neville Pinto; Panagiotis Smirniotis; Stephen Thiel

2010-08-31T23:59:59.000Z

198

Urinary 1-hydroxypyrene in nonsmokers: a biomarker for coke smoke exposure and general urban PAH exposure.  

E-Print Network (OSTI)

??This dissertation research examined the validity of urinary 1-OHP as a biomarker of PAH for coke production workers and non-coke oven workers in Anshan City,… (more)

Han, In-Kyu

2008-01-01T23:59:59.000Z

199

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

200

The Iron Age & Coal-based Coke: A Neglected Case of Fossil-fuel Dependence  

E-Print Network (OSTI)

The Iron Age & Coal-based Coke: A Neglected Case of Fossil-fuel Dependence by Vaclav Smil September share of their primary energies from renewable sources. Steel & Coal-Derived Coke Here is another important: steel's fundamental dependence on coal-derived coke with no practical substitutes on any rational

Smil, Vaclav

Note: This page contains sample records for the topic "remove carbon coke" 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

Co-combustion Character of Oil Shale and Its Semi-coke on CFB Bench  

Science Conference Proceedings (OSTI)

Semi-coke is by-product from oil shale retorts and it is important to burn it in CFB furnace. But limited to the inflammable combustion traits, co-combustion of semi-coke with raw oil shale would be meaningful. Experimental research on co-combustion ... Keywords: combustion, distribution, semi-coke, temperature

Sun Baizhong; Huang Zhirong

2011-08-01T23:59:59.000Z

202

Cracking of simulated oil refinery off-gas over a coal char, petroleum coke, and quartz  

Science Conference Proceedings (OSTI)

The cracking of oil refinery off-gas, simulated with a gas mixture containing methane (51%), ethylene (21.4%), ethane (21.1%), and propane (6.5%), over a coal char, petroleum coke, and quartz, respectively, has been studied in a fixed bed reactor. The experiments were performed at temperatures between 850 and 1000{sup o}C and at atmospheric pressure. The results show that the conversions of all species considered increased with increasing temperature. Ethane and propane completely decomposed over all three bed materials in the temperature range investigated. However, the higher initial conversion rates of methane and ethylene cracking at all temperatures were observed only over the coal char and not on the petroleum coke and quartz, indicating a significant catalytic effect of the coal char on methane and ethylene cracking. Methane and ethylene conversions decreased with reaction time due to deactivation of the coal char by carbon deposition on the char surface and, in the later stage of a cracking experiment, became negative, suggesting that methane and ethylene had been formed during the cracking of ethane and propane. 16 refs., 13 figs., 2 tabs.

Yuan Zhang; Jin-hu Wu; Dong-ke Zhang [Chinese Academy of Sciences, Taiyuan (China). Institute of Coal Chemistry

2008-03-15T23:59:59.000Z

203

Process for separating, especially in multiple stages, acid components such as CO/sub 2/, HCN and specifically H/sub 2/S, from gases, especially from coke oven gases, by means of ammonia recirculation scrubbing  

SciTech Connect

A process of separating in multiple stages acid components in coke oven gas such as CO/sub 2/, HCN and particularly H/sub 2/S by ammonia scrubbing wherein the ammonia used in scrubbing is deacidified to remove the acid components and is recirculated to the scrubbing process at least in part as substantially pure liquid ammonia.

Bauer, H.K.; Otte, E.A.W.

1984-10-16T23:59:59.000Z

204

Theoretical and experimental foundations for preparing coke for blast-furnace smelting  

SciTech Connect

This article examines the preparation of coke for blast-furnace smelting by a method that most fully meets the requirements of blast-furnace technology: screening of the -36 mm fraction, the separation of nut coke of the 15-36 mm fraction, and its charging into the furnace in a mixture with the iron-ore-bearing charge components. An analysis is made of trial use of coke of the Premium class on blast furnace No. 5 at the Enakievo Metallurgical Plant. Use of this coke makes it possible to reduce the consumption of skip coke by 3.2-4.1%.

A.L. Podkorytov; A.M. Kuznetsov; E.N. Dymchenko; V.P. Padalka; S.L. Yaroshevskii; A.V. Kuzin [Enakievo Metallurgical Plant, Enakievo (Ukraine)

2009-05-15T23:59:59.000Z

205

Coke battery with 51-m{sup 3} furnace chambers and lateral supply of mixed gas  

SciTech Connect

The basic approaches employed in the construction of coke battery 11A at OAO Magnitogorskii Metallurgicheskii Kombinat are outlined. This battery includes 51.0-m{sup 3} furnaces and a dust-free coke-supply system designed by Giprokoks with lateral gas supply; it is heated exclusively by low-calorific mixed gas consisting of blast-furnace gas with added coke-oven gas. The 82 furnaces in the coke battery are divided into two blocks of 41. The gross coke output of the battery (6% moisture content) is 1140000 t/yr.

V.I. Rudyka; N.Y. Chebotarev; O.N. Surenskii; V.V. Derevich [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

206

Temperature-programmed decomposition desorption of mercury species over activated carbon sorbents for mercury removal from coal-derived fuel gas  

Science Conference Proceedings (OSTI)

The mercury (Hg{sup 0}) removal process for coal-derived fuel gas in the integrated gasification combined cycle (IGCC) process will be one of the important issues for the development of a clean and highly efficient coal power generation system. Recently, iron-based sorbents, such as iron oxide (Fe{sub 2}O{sub 3}), supported iron oxides on TiO{sub 2}, and iron sulfides, were proposed as active mercury sorbents. The H{sub 2}S is one of the main impurity compounds in coal-derived fuel gas; therefore, H{sub 2}S injection is not necessary in this system. HCl is also another impurity in coal-derived fuel gas. In this study, the contribution of HCl to the mercury removal from coal-derived fuel gas by a commercial activated carbon (AC) was studied using a temperature-programmed decomposition desorption (TPDD) technique. The TPDD technique was applied to understand the decomposition characteristics of the mercury species on the sorbents. The Hg{sup 0}-removal experiments were carried out in a laboratory-scale fixed-bed reactor at 80-300{sup o}C using simulated fuel gas and a commercial AC, and the TPDD experiments were carried out in a U-tube reactor in an inert carrier gas (He or N{sub 2}) after mercury removal. The following results were obtained from this study: (1) HCl contributed to the mercury removal from the coal-derived fuel gas by the AC. (2) The mercury species captured on the AC in the HCl{sup -} and H{sub 2}S-presence system was more stable than that of the H{sub 2}S-presence system. (3) The stability of the mercury surface species formed on the AC in the H{sub 2}S-absence and HCl-presence system was similar to that of mercury chloride (HgClx) species. 25 refs., 12 figs., 1 tab.

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

2009-09-15T23:59:59.000Z

207

Process for converting coal into liquid fuel and metallurgical coke  

DOE Patents (OSTI)

A method of recovering coal liquids and producing metallurgical coke utilizes low ash, low sulfur coal as a parent for a coal char formed by pyrolysis with a volatile content of less than 8%. The char is briquetted and heated in an inert gas over a prescribed heat history to yield a high strength briquette with less than 2% volatile content.

Wolfe, Richard A. (Abingdon, VA); Im, Chang J. (Abingdon, VA); Wright, Robert E. (Bristol, TN)

1994-01-01T23:59:59.000Z

208

Fuel gas main replacement at Acme Steel's coke plant  

SciTech Connect

ACME Steel's Chicago coke plant consists of two 4-meter, 50-oven Wilputte underjet coke-oven batteries. These batteries were constructed in 1956--1957. The use of blast furnace gas was discontinued in the late 1960's. In 1977--1978, the oven walls in both batteries were reconstructed. Reconstruction of the underfire system was limited to rebuilding the coke-oven gas reversing cocks and meter in orifices. By the early 1980's, the 24-in. diameter underfire fuel gas mains of both batteries developed leaks at the Dresser expansion joints. These leaks were a result of pipe loss due to corrosion. Leaks also developed along the bottoms and sides of both mains. A method is described that permitted pushing temperatures to be maintained during replacement of underfire fuel gas mains. Each of Acme's two, 50-oven, 4-metric Wilputte coke-oven, gas-fired batteries were heated by converting 10-in. diameter decarbonizing air mains into temporary fuel gas mains. Replacement was made one battery at a time, with the temporary 10-in. mains in service for five to eight weeks.

Trevino, O. (Acme Steel Co., Chicago, IL (United States). Chicago Coke Plant)

1994-09-01T23:59:59.000Z

209

Table 23. Coal Receipts at Coke Plants by Census Division  

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

Receipts at Coke Plants by Census Division Receipts at Coke Plants by Census Division (thousand short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Table 23. Coal Receipts at Coke Plants by Census Division (thousand short tons) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Year to Date Census Division April - June 2013 January - March 2013 April - June 2012 2013 2012 Percent Change Middle Atlantic w w w w w w East North Central 3,189 2,679 3,225 5,867 5,993 -2.1 South Atlantic w w w w w w East South Central w w w w w w U.S. Total 5,770 4,962 5,370 10,732 10,440 2.8 w = Data withheld to avoid disclosure. Note: Total may not equal sum of components because of independent rounding. Source: U.S. Energy Information Administration (EIA), Form EIA-5, 'Quarterly Coal Consumption and Quality Report - Coke Plants

210

Coke quality for blast furnaces with coal-dust fuel  

SciTech Connect

Recently, plans have been developed for the introduction of pulverized coal injection (PCI) at various Russian metallurgical enterprises. The main incentive for switching to PCI is the recent price rises for Russian natural gas. The paper discusses the quality of coke for PCI into blast furnaces.

Y.A. Zolotukhin; N.S. Andreichikov [Eastern Coal-Chemistry Institute, Yekaterinburg (Russian Federation)

2009-07-01T23:59:59.000Z

211

The development of coke smelting and the industrial revolution  

E-Print Network (OSTI)

Abraham Darby and the origins of the industrial revolution in Britain. Alan Macfarlane talks to John about the reasons for the area near Birmingham becoming the epi-centre of the industrial development, and the development of coke furnaces and iron...

Macfarlane, Alan

2004-08-05T23:59:59.000Z

212

U.S. Refinery Yield of Petroleum Coke (Percent)  

U.S. Energy Information Administration (EIA)

U.S. Refinery Yield of Petroleum Coke (Percent) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9; 1990's: 4.3: 4.3: 4.3: ...

213

U.S. Refinery Yield of Petroleum Coke (Percent)  

U.S. Energy Information Administration (EIA)

U.S. Refinery Yield of Petroleum Coke (Percent) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec; 1993: 4.4: 4.6: 4.5: 4.3: 4.1: 4.2: 4.4: 4.3: ...

214

Vacuum carbonate desulfurization and claus sulfur recovery system at No. 11 battery  

Science Conference Proceedings (OSTI)

The vacuum carbonate process functions above 90% efficiency and satisfactorily removes the HCN and sulfur compounds from the coke oven gas generated at No. 11 Battery. It has been noted that a large quantity of energy is required for the operation of the vacuum carbonate system. Normally 544,617 kg (1.2 million lbs of steam) and 5.4 thousand kWh of electricity are used per day to maintain the system's temperatures and pressures. The processed coke oven gases from the system satisfy industrial and environmental standards as a combustible fuel. The HCN destruction unit reduces the corrosive HCN to concentrations below .07% of the acid gas stream and offers the necessary protection to the downstream modified Claus unit. The Claus unit at No. 11 Battery operates at 98% efficiency and produces 5896 kg (6.5 tons) of sulfur per day. The liquid sulfur generated in the Claus unit is a high quality product of 99% purity. 7 figures, 3 tables.

Ellis, A.

1981-01-01T23:59:59.000Z

215

A Different Strategy to Use Low Sulfur Cokes at Alumar Coke ...  

Science Conference Proceedings (OSTI)

This paper presents an alternative strategy to Alumar's blending facility. ... from Coal (3) - Carbonization Properties of Hypercoal Blended with Coal-Tar Pitch.

216

Understanding the Adsorption of Polycyclic Aromatic Hydrocarbons from Aqueous Phase onto Activated Carbon.  

E-Print Network (OSTI)

??Non-competitive adsorption of polycyclic aromatic hydrocarbons (PAHs) from water onto activated carbon was studied alongside the performance of CO2-activated petroleum coke as a low-cost adsorbent.… (more)

Awoyemi, Ayodeji

2011-01-01T23:59:59.000Z

217

Coke County, Texas: Energy Resources | Open Energy Information  

Open Energy Info (EERE)

Coke County, Texas: Energy Resources Coke County, Texas: Energy Resources Jump to: navigation, search Equivalent URI DBpedia Coordinates 31.8277663°, -100.5296115° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":31.8277663,"lon":-100.5296115,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

218

Development of Load Tap Changer Monitoring Technique: Mechanism of Coking  

Science Conference Proceedings (OSTI)

Load tap changers (LTCs) play a major role in the reliable delivery of electric power. They are the single biggest contributors to transformer outages. To improve reliability and extend their service interval, utilities are adopting proactive maintenance practices using monitoring devices and seeking new diagnostic techniques. As part of an ongoing EPRI project, EPRI and cosponsor Consolidated Edison Co. of New York, Inc. engaged in a study of contact coking, one of the biggest problems in LTCs. This EPR...

2001-11-27T23:59:59.000Z

219

New environmental concepts in the chemical and coke industries  

Science Conference Proceedings (OSTI)

We know that environmentally pure technologies do not exist. Coke production is no exception to the rule. The article considers the logic of environmental decision making. Attention focuses on a new bank of ecologically appropriate materials whose release to the biosphere must be considered solely in quantititative terms. Qualitativily all these materials are familiar; they are assimilated by populations of microorganisms and tar thus compatible with the biosphere.

A.Yu. Naletov; V.A. Naletov [Mendeleev Russian Chemical-Engineering University (Russian Federation)

2007-05-15T23:59:59.000Z

220

Table 17. Average Price of U.S. Coke Exports  

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

Average Price of U.S. Coke Exports Average Price of U.S. Coke Exports (dollars per short ton) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Table 17. Average Price of U.S. Coke Exports (dollars per short ton) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Year to Date Continent and Country of Destination April - June 2013 January - March 2013 April - June 2012 2013 2012 Percent Change North America Total 240.59 241.38 218.40 240.85 225.80 6.7 Canada* 147.49 330.47 243.04 183.08 286.56 -36.1 Mexico 316.57 211.63 189.12 273.97 171.71 59.6 Other** 612.42 485.63 134.48 525.92 135.04 289.5 South America Total 140.65 156.15 322.70 148.29 250.36 -40.8 Other** 140.65 156.15 322.70 148.29 250.36 -40.8 Europe Total 259.26 255.24 - 257.06 427.83 -39.9 Other**

Note: This page contains sample records for the topic "remove carbon coke" 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

Table 22. Average Price of U.S. Coke Imports  

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

Average Price of U.S. Coke Imports Average Price of U.S. Coke Imports (dollars per short ton) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Table 22. Average Price of U.S. Coke Imports (dollars per short ton) U.S. Energy Information Administration | Quarterly Coal Report, April - June 2013 Year to Date Continent and Country of Origin April - June 2013 January - March 2013 April - June 2012 2013 2012 Percent Change North America Total 263.21 252.66 353.05 261.29 356.01 -26.6 Canada 263.51 252.66 353.05 258.82 356.01 -27.3 Panama 263.09 - - 263.09 - - South America Total 196.86 194.14 175.88 195.94 181.01 8.2 Brazil - - 157.60 - 157.60 - Colombia 196.86 194.14 322.06 195.94 246.68 -20.6 Europe Total 181.55 232.13 385.65 225.53 384.96 -41.4 Czech Republic - 475.91 - 475.91 - - Spain 360.51

222

The Vertical Ball Mill for the Grinding of Calcined Petroleum Coke to ...  

Science Conference Proceedings (OSTI)

A new vertical ball ring mill concept has been developed based on the results of research on the grinding of calcined petroleum coke. Industrial vertical mills are ...

223

Development Of Reclamation Substrates For Alberta Oil Sands Using Mature Fine Tailings And Coke.  

E-Print Network (OSTI)

??Mature fine tailings and coke are waste products of the oil sands industry with potential for reclamation. A greenhouse study assessed whether substrates of various… (more)

Luna-Wolter, Gabriela L.

2012-01-01T23:59:59.000Z

224

Lignin as Both Fuel and Fusing Binder in Briquetted Anthracite Fines for Foundry Coke Substitute.  

E-Print Network (OSTI)

??Lignin that had been extracted from Kraft black liquor was investigated as a fusing binder in briquetted anthracite fines for a foundry coke substitute. Cupola… (more)

Lumadue, Matthew

2012-01-01T23:59:59.000Z

225

Coke yield and transport processes in agglomerates of bitumen and solids.  

E-Print Network (OSTI)

??Agglomerate formation is a common phenomenon that can cause operating problems in the fluid coking reactor. When agglomerates form they provide longer diffusion paths of… (more)

Ali, Mohamed Ali Hassan

2010-01-01T23:59:59.000Z

226

The Effect of Coke Particle Size on Thermal Profile of Sintering ...  

Science Conference Proceedings (OSTI)

Baking process and sinter production was performed for different ranges of coke particle size while other parameter like, iron ore, lime and sintering mixture ...

227

U.S. Exports to Belarus of Petroleum Coke (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

U.S. Exports to Belarus of Petroleum Coke (Thousand Barrels) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec; 2004: 17

228

Co-gasification of biomass with coal and oil sands coke in a drop tube furnace.  

E-Print Network (OSTI)

??Chars were obtained from individual fuels and blends with different blend ratios of coal, coke and biomass in Drop Tube Furnace at different temperatures. Based… (more)

Gao, Chen

2010-01-01T23:59:59.000Z

229

Pyrolysis behavior of coal and petroleum coke at high temperature and high pressure.  

E-Print Network (OSTI)

??While pyrolysis of coal is a well-studied thermal process, little is known about pressurized pyrolysis of coal and petroleum coke. This study aims to interpret… (more)

Wagner, David Ray

2011-01-01T23:59:59.000Z

230

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

231

Determination of the effect of different additives in coking blends using a combination of in situ high-temperature {sup 1}H NMR and rheometry  

SciTech Connect

High-temperature {sup 1}H NMR and rheometry measurements were carried out on 4:1 wt/wt blends of a medium volatile bituminous coal with two anthracites, two petroleum cokes, charcoal, wood, a low-temperature coke breeze, tyre crumb, and active carbon to determine the effects on fluidity development to identify the parameters responsible for these effects during pyrolysis and to study possible relationships among the parameters derived from these techniques. Positive, negative, and neutral effects were identified on the concentration of fluid material. Small positive effects (ca. 5-6%) were caused by blending the coal with petroleum cokes. Charcoal, wood, and active carbon all exerted negative effects on concentration (18-27% reduction) and mobility (12-25% reduction in T2) of the fluid phase, which have been associated with the inert character and high surface areas of these additives that adsorb the fluid phase of the coal. One of the anthracites and the low-temperature coke breeze caused deleterious effects to a lesser extent on the concentration (7-12%) and mobility (13-17%) of the fluid material, possibly due to the high concentration of metals in these additives (ca. 11% ash). Despite the high fluid character of tyre crumb at the temperature of maximum fluidity of the coal (73%), the mobility of the fluid phase of the blend was lower than expected. The comparison of {sup 1}H NMR and rheometry results indicated that to account for the variations in minimum complex viscosity for all the blends, both the maximum concentration of fluid phase and the maximum mobility of the fluid material had to be considered. For individual blends, two exponential relationships have been found between the complex viscosity and the concentration of solid phase in both the softening and resolidification stages but the parameters are different for each blend. 30 refs., 8 figs., 5 tabs.

Miguel C. Diaz; Karen M. Steel; Trevor C. Drage; John W. Patrick; Colin E. Snape [Nottingham University, Nottingham (United Kingdom). Nottingham Fuel and Energy Centre, School of Chemical, Environmental and Mining Engineering

2005-12-01T23:59:59.000Z

232

Developing indicators for the assessment and proper management of the different levels of exposure to polycyclic aromatic hydrocarbons (PAH)s generally associated with coke-oven workers.  

E-Print Network (OSTI)

??Coke ovens may occur in the aluminium, steel, graphite, electrical, and construction industries. In the work area coke-oven workers may be exposed to various chemical… (more)

Wang, Tianyuan

2011-01-01T23:59:59.000Z

233

Enhanced carbon monoxide utilization in methanation process  

DOE Green Energy (OSTI)

Carbon monoxide - containing gas streams are passed over a catalyst to deposit a surface layer of active surface carbon thereon essentially without the formation of inactive coke. The active carbon is subsequently reacted with steam or hydrogen to form methane. Surprisingly, hydrogen and water vapor present in the feed gas do not adversely affect CO utilization significantly, and such hydrogen actually results in a significant increase in CO utilization.

Elek, Louis F. (Peekskill, NY); Frost, Albert C. (Congers, NY)

1984-01-01T23:59:59.000Z

234

Process for producing methane from gas streams containing carbon monoxide and hydrogen  

DOE Patents (OSTI)

Carbon monoxide-containing gas streams are passed over a catalyst capable of catalyzing the disproportionation of carbon monoxide so as to deposit a surface layer of active surface carbon on the catalyst essentially without formation of inactive coke thereon. The surface layer is contacted with steam and is thus converted to methane and CO.sub.2, from which a relatively pure methane product may be obtained. While carbon monoxide-containing gas streams having hydrogen or water present therein can be used only the carbon monoxide available after reaction with said hydrogen or water is decomposed to form said active surface carbon. Although hydrogen or water will be converted, partially or completely, to methane that can be utilized in a combustion zone to generate heat for steam production or other energy recovery purposes, said hydrogen is selectively removed from a CO--H.sub.2 -containing feed stream by partial oxidation thereof prior to disproportionation of the CO content of said stream.

Frost, Albert C. (Congers, NY)

1980-01-01T23:59:59.000Z

235

The effects of petroleum coke amendments on macrophytes and aquatic invertebrates in northern Alberta, Canada constructed wetlands.  

E-Print Network (OSTI)

??Oil-sands operators of Fort McMurray, Alberta produce six million t/y of petroleum coke. The use of coke to stabilize clay-dominated mine tailings in constructed wetlands… (more)

Baker, Leanne F.

2007-01-01T23:59:59.000Z

236

Industrial Carbon Management Initiative (ICMI)  

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

Industrial Carbon Management Initiative Industrial Carbon Management Initiative (ICMI) Background The ICMI project is part of a larger program called Carbon Capture Simulation and Storage Initiative (C2S2I). The C2S2I has a goal of expanding the DOE's focus on Carbon Capture Utilization and Storage (CCUS) for advanced coal power systems and other applications, including the use of petroleum coke as a feedstock for the industrial sector. The American Recovery and Re-Investment Act (ARRA)-funded

237

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

238

Short Survey: Intelligent switching expert system for delayed coking unit based on iterative learning strategy  

Science Conference Proceedings (OSTI)

Delayed coking is the most effective process to decarbonize and demetallize heavy petroleum residues. However, it relies much on the field engineers' experiences and expertise in practice for operating the controllers effectively and compatibly in delayed ... Keywords: Delayed coking, Expert system, Intelligent control, Iterative learning

Xiaodong Yu; Yujie Wei; Dexian Huang; Yongheng Jiang; Bo Liu; Yihui Jin

2011-07-01T23:59:59.000Z

239

Study on Further Treatment of Coal Coking Wastewater by Ultrasound Wave, Fenton's Reagent and Coagulation  

Science Conference Proceedings (OSTI)

The study on further treatment of coal coking wastewater by ultrasound wave, Fenton's reagent and coagulation was carried out in this paper at the first time, Furthermore, this paper discussed the optimum cooperative reaction condition of their combined ... Keywords: ultrasound wave, coke plant wastewater, Fenton reagent, coagulation

Jun Shi; Liangbo Zhang

2009-10-01T23:59:59.000Z

240

Organic Sulphur Transfers in Coke Oven Gas via Noncatalytic Partial Oxidation  

Science Conference Proceedings (OSTI)

The organic sulfur transformation was studied during coke oven gas to produce syngas via noncatalytic partial oxidation. The concentration of CS2 and thiophene was examined in syngas by sulfide detector. For comparison, the sulfur transfer was also studied ... Keywords: Organic sulfur transfer, Coke oven gas, CS2, thiophene

Guojie Zhang; Yongfa Zhang; Xianglan Li; Hongcheng Cao

2009-10-01T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

Analytical input-output and supply chain study of China's coke and steel sectors  

E-Print Network (OSTI)

I design an input-output model to investigate the energy supply chain of coal-coke-steel in China. To study the demand, supply, and energy-intensity issues for coal and coke from a macroeconomic perspective, I apply the ...

Li, Yu, 1976-

2004-01-01T23:59:59.000Z

242

Influence of coal on coke properties and blast-furnace operation  

SciTech Connect

With unstable coal supplies and properties and a fluctuating content of coking coal in the batch at OAO Zapadno-Sibirskii Metallurgicheskii Kombinat (ZSMK) and of bituminous coal at Kuznetskaya enrichment facility, it is important to optimize the rank composition of the batch for coke production.

G.R. Gainieva; L.D. Nikitin [OAO Zapadno-Sibirskii Metallurgicheskii Kombinat (Russian Federation)

2007-07-01T23:59:59.000Z

243

Analytical input-output and supply chain study of China's coke and steel sectors; Analytical I/O and supply chain study of China's coke and steel sectors.  

E-Print Network (OSTI)

??I design an input-output model to investigate the energy supply chain of coal-coke-steel in China. To study the demand, supply, and energy-intensity issues for coal… (more)

Li, Yu, 1976-

2004-01-01T23:59:59.000Z

244

Bethlehem Steel announces plans to control coke oven air and water pollution  

Science Conference Proceedings (OSTI)

Bethlehem Steel Corporation and the Maryland Department of the Environment have announced an agreement under which Bethlehem will spend an estimated $92-million at its Sparrows Points, Md., plant for technologically-advanced controls to further reduce air and water pollution, mainly from the plant's coke ovens. The two major systems include one to treat by-product coke oven gas and chemicals, and another to upgrade existing pushing emission controls on two older coke oven batteries. One of the new systems will replace most of the existing equipment that cleans gas and treats chemicals created by the coking process at the plant's three coke oven batteries. Because this system has the potential to greatly reduce sulfur dioxide and other pollutants, the United States Department of Energy (DOE) in September announced that its installation qualified for funding as part of the nationwide Innovative Clean Coal Technology Program.

Not Available

1989-08-01T23:59:59.000Z

245

Spring 2009 Vol.33, No.1 Nearly beardless V. A. sp. nor., with spotted spur (petal removed)  

E-Print Network (OSTI)

Clarke Susan Coale Janice M. Cockren Barbara Coe Dale Coke Madelene Coke Sharon Cooper Barbara Cordes

California at Santa Cruz, University of

246

JV Task 90 - Activated Carbon Production from North Dakota Lignite  

Science Conference Proceedings (OSTI)

The Energy & Environmental Research Center (EERC) has pursued a research program for producing activated carbon from North Dakota lignite that can be competitive with commercial-grade activated carbon. As part of this effort, small-scale production of activated carbon was produced from Fort Union lignite. A conceptual design of a commercial activated carbon production plant was drawn, and a market assessment was performed to determine likely revenue streams for the produced carbon. Activated carbon was produced from lignite coal in both laboratory-scale fixed-bed reactors and in a small pilot-scale rotary kiln. The EERC was successfully able to upgrade the laboratory-scale activated carbon production system to a pilot-scale rotary kiln system. The activated carbon produced from North Dakota lignite was superior to commercial grade DARCO{reg_sign} FGD and Rheinbraun's HOK activated coke product with respect to iodine number. The iodine number of North Dakota lignite-derived activated carbon was between 600 and 800 mg I{sub 2}/g, whereas the iodine number of DARCO FGD was between 500 and 600 mg I{sub 2}/g, and the iodine number of Rheinbraun's HOK activated coke product was around 275 mg I{sub 2}/g. The EERC performed both bench-scale and pilot-scale mercury capture tests using the activated carbon made under various optimization process conditions. For comparison, the mercury capture capability of commercial DARCO FGD was also tested. The lab-scale apparatus is a thin fixed-bed mercury-screening system, which has been used by the EERC for many mercury capture screen tests. The pilot-scale systems included two combustion units, both equipped with an electrostatic precipitator (ESP). Activated carbons were also tested in a slipstream baghouse at a Texas power plant. The results indicated that the activated carbon produced from North Dakota lignite coal is capable of removing mercury from flue gas. The tests showed that activated carbon with the greatest iodine number was superior to commercial DARCO FGD for mercury capture. The results of the activated carbon market assessment indicate an existing market for water treatment and an emerging application for mercury control. That market will involve both existing and new coal-fired plants. It is expected that 20% of the existing coal-fired plants will implement activated carbon injection by 2015, representing about 200,000 tons of annual demand. The potential annual demand by new plants is even greater. In the mercury control market, two characteristics are going to dominate the customer's buying habit-performance and price. As continued demonstration testing of activated carbon injection at the various coal-fired power plants progresses, the importance of fuel type and plant configuration on the type of activated carbon best suited is being identified.

Steven Benson; Charlene Crocker; Rokan Zaman; Mark Musich; Edwin Olson

2008-03-31T23:59:59.000Z

247

Ion Removal  

INL’s ion removal technology leverages the ability of phosphazene polymers discriminate between water and metal ions, which allows water to pass ...

248

Innovative coke oven gas cleaning system for retrofit applications: Environmental Monitoring Program. Volume 3, Appendix sections 8--14: Baseline Sampling Program report  

Science Conference Proceedings (OSTI)

This report contains no text. It consists entirely of numerical data: Coke oven wastewater treatment performance; Ammonia still effluents to equalization tank; Stack gas analysis of coke oven batteries; CoaL consumption; Coke production; Supplemental OSHA employee exposure monitoring(hydrocarbons,ammonia, hydrogen sulfide); operating data; chemical products and coke oven gas production.

Stuart, L.M.

1994-05-27T23:59:59.000Z

249

Annual book of ASTM Standards 2008. Section Five. Petroleum products, lubricants, and fossil fuels. Volume 05.06. Gaseous fuels; coal and coke  

SciTech Connect

The first part covers standards for gaseous fuels. The second part covers standards on coal and coke including the classification of coals, determination of major elements in coal ash and trace elements in coal, metallurgical properties of coal and coke, methods of analysis of coal and coke, petrogrpahic analysis of coal and coke, physical characteristics of coal, quality assurance and sampling.

NONE

2008-09-15T23:59:59.000Z

250

Laser ultrasonic furnace tube coke monitor. Quarterly technical progress report No. 1, May 1--August 1, 1998  

Science Conference Proceedings (OSTI)

The overall aim of the project is to demonstrate the performance and practical use of a laser ultrasonic probe for measuring the thickness of coke deposits located within the high temperature tubes of a thermal cracking furnace. This aim will be met by constructing an optical probe that will be tested using simulated coke deposits that are positioned inside of a bench-scale furnace. Successful development of the optical coke detector will provide industry with the only available method for on-line measurement of coke deposits. The optical coke detector will have numerous uses in the refining and petrochemical sectors including monitoring of visbreakers, hydrotreaters, delayed coking units, vacuum tower heaters, and various other heavy oil heating applications where coke formation is a problem. The coke detector will particularly benefit the olefins industry where high temperature thermal crackers are used to produce ethylene, propylene, butylene and other important olefin intermediates. The ethylene industry requires development of an on-line method for gauging the thickness of coke deposits in cracking furnaces because the current lack of detailed knowledge of coke deposition profiles introduces the single greatest uncertainty in the simulation and control of modern cracking furnaces. The laser ultrasonic coke detector will provide operators with valuable new information allowing them to better optimize the decoking turnaround schedule and therefore maximize production capacity.

NONE

1998-08-15T23:59:59.000Z

251

Characterization of liquids derived from laboratory coking of decant oil and co-coking of Pittsburgh seam bituminous coal with decant oil  

Science Conference Proceedings (OSTI)

In this study, decant oil and a blend of Pittsburgh seam bituminous coal with decant oil were subjected to coking and co-coking in a laboratory-scale delayed coker. Higher yields of coke and gas were obtained from co-coking than from coking. Coal addition into the feedstock resulted in lighter overhead liquid. GC/MS analyses of gasoline, jet fuel, and diesel show that co-coking of coal/decant oil gave higher quantity aromatic components than that of coking of decant oil alone. Simulated distillation gas chromatography analyses of overhead liquids and GC/MS analyses of vacuum fractions show that when coal was reacted with a decant oil, the coal constituents contributed to the distillable liquids. To address the reproducibility of the liquid products, overhead liquid samples collected at the first, third, and fifth hours of experiments of 6 h duration were evaluated using simulated distillation gas chromatography and {sup 1}H and {sup 13}C NMR. NMR analyses of the liquid products showed that, even though there were slight changes in the {sup 1}H and {sup 13}C spectra, the standard deviation was low for the time-dependent samples. Simulated distillation gas chromatography showed that the yields of refinery boiling range materials (i.e., gasoline, jet fuel, diesel, and fuel oil cuts) were reproducible between runs. Fractionation of the overhead liquids into refinery boiling range materials (gasoline, jet fuel, diesel, fuel oil fractions) showed that the boiling range materials and chemical compositions of fractions were found to be reproducible. 54 refs., 17 tabs.

Omer Gul; Caroline Clifford; Leslie R. Rudnick; Harold H. Schobert [Pennsylvania State University, University Park, PA (United States)

2009-05-15T23:59:59.000Z

252

Effects of HyperCoal addition on coke strength and thermoplasticity of coal blends  

SciTech Connect

Ashless coal, also known as HyperCoal (HPC), was produced by thermal extraction of three coals of different ranks (Gregory caking coal, Warkworth steam coal, and Pasir subbituminous coal) with 1-methylnaphthalene (1-MN) at 360, 380, and 400{sup o}C. The effects of blending these HPCs into standard coal blends were investigated. Blending HPCs as 5-10% of a standard blend (Kouryusho:Goonyella:K9) enhanced the thermoplasticity over a wide temperature range. For blends made with the Pasir-HPC, produced from a noncaking coal, increasing the extraction temperature from 360 to 400{sup o}C increased the thermoplasticity significantly. Blends containing Warkworth-HPC, produced from a slightly caking coal, had a higher tensile strength than the standard blend in semicoke strength tests. The addition of 10% Pasir-HPC, extracted at 400{sup o}C, increased the tensile strength of the semicokes to the same degree as those made with Gregory-HPC. Furthermore, all HPC blends had a higher tensile strength and smaller weight loss during carbonization. These results suggest that the HPC became integrated into the coke matrix, interacting strongly with the other raw coals. 14 refs., 11 figs., 1 tab.

Toshimasa Takanohashi; Takahiro Shishido; Ikuo Saito [National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba (Japan). Energy Technology Research Institute

2008-05-15T23:59:59.000Z

253

Energy efficiency of alternative coke-free metallurgical technologies  

SciTech Connect

Energy analysis is undertaken for the blast-furnace process, for liquid-phase processes (Corex, Hismelt, Romelt), for solid-phase pellet reduction (Midrex, HYL III, LP-V in a shaft furnace), for steel production in systems consisting of a blast furnace and a converter, a Midrex unit and an arc furnace, or a Romelt unit and an arc furnace, and for scrap processing in an arc furnace or in an LP-V shaft furnace. Three blast-furnace processes with sinter and coke are adopted as the basis of comparison, as in: the standard blast-furnace process used in Russia; the improved blast-furnace process with coal-dust injection; and the production of vanadium hot metal from vanadium-bearing titanomagnetite ore (with a subsequent duplex process, ferrovanadium production, and its use in the arc furnace).

V.G. Lisienko; A.V. Lapteva; A.E. Paren'kov [Ural State Technical University - Ural Polytechnic Institute, Yekaterinburg (Russian Federation)

2009-02-15T23:59:59.000Z

254

Cogeneration Waste Heat Recovery at a Coke Calcining Facility  

E-Print Network (OSTI)

PSE Inc. recently completed the design, construction and start-up of a cogeneration plant in which waste heat in the high temperature flue gases of three existing coke calcining kilns is recovered to produce process steam and electrical energy. The heat previously exhausted to the atmosphere is now converted to steam by waste heat recovery boilers. Eighty percent of the steam produced is metered for sale to a major oil refinery, while the remainder passes through a steam turbine generator and is used for deaeration and feedwater heating. The electricity produced is used for the plant auxiliaries and sold to the local utility. Many design concepts were incorporated into the plant which provided for high plant availability, reliability and energy efficiency. This paper will show how these concepts were implemented and incorporated into the detailed design of the plant while making cogeneration a cost effective way to save conventional fuels. Operating data since plant start-up will also be presented.

Coles, R. L.

1986-06-01T23:59:59.000Z

255

Method of removing contaminants from plastic resins  

DOE Patents (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee' s Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-11-18T23:59:59.000Z

256

Method for removing contaminants from plastic resin  

Science Conference Proceedings (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-12-30T23:59:59.000Z

257

Method of removing contaminants from plastic resins  

Science Conference Proceedings (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert,George W. (Harrisonville, MO); Hand,Thomas E. (Lee's Summit, MO); Delaurentiis,Gary M. (Jamestown, CA)

2007-08-07T23:59:59.000Z

258

Co-Gasification Behavior of Metallurgical Coke with High and Low ...  

Science Conference Proceedings (OSTI)

The co-gasification behavior of highly and lowly reactive coke for blast furnace is investigated. ... Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy .... Thermal Plasma Torches for Metallurgical Applications.

259

Current developments at Giprokoks for coke-battery construction and reconstruction  

Science Conference Proceedings (OSTI)

Approaches developed at Giprokoks for coke-battery construction and reconstruction are considered. Recommendations regarding furnace construction and reconstruction are made on the basis of Ukrainian and world experience.

V.I. Rudyka; Y.E. Zingerman; V.B. Kamenyuka; O.N. Surenskii; G.E. Kos'kova; V.V. Derevich; V.A. Gushchin [Giprokoks, the State Institute for the Design of Coke-Industry Enterprises, Kharkov (Ukraine)

2009-07-15T23:59:59.000Z

260

Guide to ASTM test methods for the analysis of coal and coke  

Science Conference Proceedings (OSTI)

The guide includes brief descriptions of all 56 ASTM test methods that cover the physical, chemical, and spectroscopic analytical techniques to qualitatively and quantitatively identify over 40 chemical and physical properties of coal, coke, their products, and by-products.

R.A. Kishore Nadkarni (ed.)

2008-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

U.S. Exports to South Africa of Petroleum Coke (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

U.S. Exports to South Africa of Petroleum Coke (Thousand Barrels) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9; ...

262

Study of ways of reducing coke use at non-integrated metallurgical plants  

SciTech Connect

To reduce the costs of blast-furnace smelting, the Svobodnyi Sokol plant has devised a comprehensive program of organizational-technical measures that include study of ways of reducing coke consumption. To do this, the plant began operating its blast furnaces with schungite when making foundry and conversion pig irons. Using schungite in the charge employed to make foundry iron makes it possible to save a significant (10-15%) amount of coke. The value of the coefficient that characterizes the replacement of coke by schungite varies broadly and can reach 1.0 or more, depending on the grade of iron being made and the furnace operating regime. The same coefficient has a value of 0.57 kg coke/kg schungite when 12-15 kg schungite/ton pig is used to make conversion pig iron.

S.A. Feshchenko; V.I. Pleshkov; I.N. Shishchuk; A.V. Buev [Svobodnyi Sokol (Russian Federation). Lipetsk Metallurgical Plant

2006-03-15T23:59:59.000Z

263

U.S. Exports to Cameroon of Petroleum Coke (Thousand Barrels)  

U.S. Energy Information Administration (EIA)

U.S. Exports to Cameroon of Petroleum Coke (Thousand Barrels) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec; 1995: 0: 0: 0: 35: 0: 0: 0: 36: ...

264

Experimental study on the effects of blast-cap configurations and charge patterns on coke descending in CDQ cooling shaft  

SciTech Connect

The coke descending behavior in a CDQ cooling shaft is studied experimentally by means of a tracing method with a digital camera. For three different blast-caps, the law of coke flow is studied under five conditions of coke charge. The experimental results show that, for the sake of the uniformity of the coke burden descending, a blast-cap with elliptical cross-section is a better choice than that with circular cross-section regardless of high or low placement. A coke charge pattern with a flat top burden surface is preferable to that with peak-valley surface, a double-peak superior to a one-peak. Trajectory and average velocity distribution of coke behavior depend weakly on whether the coke is continuously fed or not as the discharging began. The blast-caps have local effects on the descending coke and hardly affect whether the cokes flow smoothly or not in the case of coke burden with enough depth.

Y.H. Feng; X.X. Zhang; M.L. Wu [University of Science & Technology, Beijing (China). School of Mechanical Engineering

2008-08-15T23:59:59.000Z

265

Development of Continuous Solvent Extraction Processes For Coal Derived Carbon Products  

DOE Green Energy (OSTI)

In this reporting period, tonnage quantities of coal extract were produced but solid separation was not accomplished in a timely manner. It became clear that the originally selected filtration process would not be effective enough for a serious commercial process. Accordingly, centrifugation was investigated as a superior means for removing solids from the extract. Results show acceptable performance. Petrographic analysis of filtered solids was carried out by R and D Carbon Petrography under the auspices of Koppers and consultant Ken Krupinski. The general conclusion is that the material appears to be amenable to centrifugation. Filtered solids shows a substantial pitch component as well as some mesophase, resulting in increased viscosity. This is likely a contributing reason for the difficulty in filtering the material. Cost estimates were made for the hydotreatment and digestion reactors that would be needed for a 20,000 ton per year demonstration plants, with the aid of ChemTech Inc. The estimates show that the costs of scaling up the existing tank reactors are acceptable. However, a strong recommendation was made to consider pipe reactors, which are thought to be more cost effective and potentially higher performance in large scale systems. The alternate feedstocks for coke and carbon products were used to fabricate carbon electrodes as described in the last quarterly report. Gregory Hackett successfully defended his MS Thesis on the use of these electrodes in Direct Carbon Fuel Cell (DCFC), which is excerpted in Section 2.4 of this quarterly report.

Elliot B. Kennel; Dady B. Dadyburjor; Gregory W. Hackett; Manoj Katakdaunde; Liviu Magean; Alfred H. Stiller; Robert C. Svensson; John W. Zondlo

2006-09-30T23:59:59.000Z

266

Metals removal from spent salts  

DOE Patents (OSTI)

A method and apparatus for removing metal contaminants from the spent salt of a molten salt oxidation (MSO) reactor is described. Spent salt is removed from the reactor and analyzed to determine the contaminants present and the carbonate concentration. The salt is dissolved in water, and one or more reagents may be added to precipitate the metal oxide and/or the metal as either metal oxide, metal hydroxide, or as a salt. The precipitated materials are filtered, dried and packaged for disposal as waste or can be immobilized as ceramic pellets. More than about 90% of the metals and mineral residues (ashes) present are removed by filtration. After filtration, salt solutions having a carbonate concentration >20% can be spray-dried and returned to the reactor for re-use. Salt solutions containing a carbonate concentration <20% require further clean-up using an ion exchange column, which yields salt solutions that contain less than 1.0 ppm of contaminants.

Hsu, Peter C. (Pleasanton, CA); Von Holtz, Erica H. (Livermore, CA); Hipple, David L. (Livermore, CA); Summers, Leslie J. (Livermore, CA); Brummond, William A. (Livermore, CA); Adamson, Martyn G. (Danville, CA)

2002-01-01T23:59:59.000Z

267

Actinide removal from spent salts  

DOE Patents (OSTI)

A method for removing actinide contaminants (uranium and thorium) from the spent salt of a molten salt oxidation (MSO) reactor is described. Spent salt is removed from the reactor and analyzed to determine the contaminants present and the carbonate concentration. The salt is dissolved in water, and one or more reagents are added to precipitate the thorium as thorium oxide and/or the uranium as either uranium oxide or as a diuranate salt. The precipitated materials are filtered, dried and packaged for disposal as radioactive waste. About 90% of the thorium and/or uranium present is removed by filtration. After filtration, salt solutions having a carbonate concentration >20% can be dried and returned to the reactor for re-use. Salt solutions containing a carbonate concentration <20% require further clean-up using an ion exchange column, which yields salt solutions that contain less than 0.1 ppm of thorium or uranium.

Hsu, Peter C. (Pleasanton, CA); von Holtz, Erica H. (Livermore, CA); Hipple, David L. (Livermore, CA); Summers, Leslie J. (Livermore, CA); Adamson, Martyn G. (Danville, CA)

2002-01-01T23:59:59.000Z

268

Development of an impedance-based sensor for the detection of catalyst coking in fuel-reforming systems.  

E-Print Network (OSTI)

??A novel sensor for detecting the early stages of catalyst coking in fuel reforming systems has been developed. The sensor was manufactured by inkjet printing… (more)

Wheeler, Jeffrey L.

2013-01-01T23:59:59.000Z

269

The Woodland Carbon Code  

E-Print Network (OSTI)

The Woodland Carbon Code While society must continue to make every effort to reduce greenhouse gas a role by removing carbon dioxide from the atmosphere. The potential of woodlands to soak up carbon to help compensate for their carbon emissions. But before investing in such projects, people want to know

270

Use of under Calcined Coke to Produce Baked Anodes for ...  

Science Conference Proceedings (OSTI)

Studies on Impact of Calcined Petroleum from Different Sources on Anode Quality · Study on Graphitization of Cathode Carbon Blocks for Aluminum Electrolysis.

271

China's Energy and Carbon Emissions Outlook to 2050  

E-Print Network (OSTI)

products such as electricity, coke, and petroleum products.efficiency levels for coke, oil refining and electricitythe energy input to producing coke dropped dramatically from

Zhou, Nan

2011-01-01T23:59:59.000Z

272

Dale Coke: Coke Farm  

E-Print Network (OSTI)

to Alice Waters’ Chez Panisse Restaurant in Berkeley, andlater other high-end restaurants across the country. Cokemostly geared toward the restaurant trade, because that’s

Farmer, Ellen

2010-01-01T23:59:59.000Z

273

Dale Coke: Coke Farm  

E-Print Network (OSTI)

the right place to get compost, or how you get the beststerilized or pasteurized our compost before we put it out.

Farmer, Ellen

2010-01-01T23:59:59.000Z

274

Innovative coke oven gas cleaning system for retrofit applications. Quarterly environmental monitoring report No. 3, January 1, 1991--December 31, 1991  

Science Conference Proceedings (OSTI)

Bethlehem Steel Corporation (BSC), in conjunction with the Department of Energy (DOE) is conducting a Clean Coal Technology (CCT) project at its Sparrows Point, Maryland Coke Oven Plant. This project combines several existing technologies into an integrated system for removing impurities from Coke Oven Gas (COG) to make it an acceptable fuel. DOE is providing cost-sharing under a Cooperative Agreement with BSC. This Cooperative Agreement requires BSC to develop and conduct an Environmental Monitoring Plan (EMP) for the Clean Coal Technology project and to report the status of the EMP on a quarterly basis. This report is the third quarterly status report of the EMP. It covers the Environmental Monitoring Plan activities for the full year of 1991 from January 1, 1991 through December 31, 1991, including the forth quarter. See Sections 2, 3 and 4 for status reports of the Project Installation and Commissioning, the Environmental Monitoring activities and the Compliance Monitoring results for the period. Section 5 contains a list of Compliance Reports submitted to regulatory agencies during the period. The EMP describes in detail the environmental monitoring activities to be performed during the project execution. The purpose of the EMP is to: (1) document the extent of compliance of monitoring activities, i.e. those monitoring required to meet permit requirements, (2) confirm the specific impacts predicted in the National Environmental Policy Act documentation, and (3) establish an information base for the assessment of the environmental performance of the technology demonstrated by the project.

Not Available

1992-10-16T23:59:59.000Z

275

What's Happening to Our Body after Drinking Coke? The Characteristic of the Blood Pressure Wave in Radial Artery  

Science Conference Proceedings (OSTI)

Previous literature has suggested that psychological state may be changed via drinking coke, however, studies empirically documenting the link between coke and blood pressure wave (BPW) are scant. Therefore, the current article attempts to explore how ... Keywords: Blood pressure wave (BPW), spectrum analysis, Sphygmogram, Traditional Chinese medicine (TCM)

Sheng-Chieh Huang; Yung-Pin Lee; Min-Hua Hsieh; Hui-Min Wang; Mark C. Hou; Shih-Chun Chao; Cheng-Lung Tseng; Wei-Ta Hsiao; Chung-Hung Hong; Kai-Yu Shao; Shi-Han Luo; Wei-Chun Chiu; Wei-Yu Chen

2011-12-01T23:59:59.000Z

276

Mechanism of physical transformations of mineral matter in the blast furnace coke with reference to its reactivity and strength  

SciTech Connect

Examinations of polished and dry cut sections of feed and tuyere coke revealed some possible mechanisms for the physical influence of mineral compounds on the reactivity and strength of coke. It was observed that rounded particles of mineral phases that are exposed to the pore walls and surface of coke at high temperature create an inorganic cover, thus reducing the surface available for gas-solid reactions. The particles of mineral matter that have a low melting point and viscosity can affect the coke at earlier stages in the blast furnace process, acting in the upper parts of the blast furnace (BF). The temperature-driven redistribution of mineral phases within the coke matrix probably leads to the creation of weak spots and in general to anisotropy in its properties, thus reducing its strength. 9 refs., 2 figs., 1 tab.

Stanislav S. Gornostayev; Jouko J. Haerkki [University of Oulu, Oulu (Finland). Laboratory of Process Metallurgy

2006-12-15T23:59:59.000Z

277

Design, construction and start-up of a modern coke plant  

Science Conference Proceedings (OSTI)

The planning and design of a 60-oven, 6m replacement coke battery and associated by-products plant for Republic Steel Corp, Chicago, are described together with the constructional methods used and problems experienced through start-up of the facility. Pushing emission control is achieved with a Mitsubishi-type land-based system and changing emission control with a Nippon Steel combination car and land-based system. A Takahax-Hirohax coke-oven gas desulphurization unit is included in the by-product plant. Construction began in March 1979 with the first push in December 1981.

Williams, A.E.

1983-05-01T23:59:59.000Z

278

NETL: News Release - NETL Patented CO2-Removal Sorbents Promise...  

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

Power and Cost Savings DOE Laboratory Signs License Agreement Incorporating Sorbents in HVAC Add-on Technology Washington, DC - Carbon dioxide removal sorbents developed by the...

279

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

280

Fabricating solid carbon porous electrodes from powders  

DOE Patents (OSTI)

Fabrication of conductive solid porous carbon electrodes for use in batteries, double layer capacitors, fuel cells, capacitive dionization, and waste treatment. Electrodes fabricated from low surface area (<50 m.sup.2 /gm) graphite and cokes exhibit excellent reversible lithium intercalation characteristics, making them ideal for use as anodes in high voltage lithium insertion (lithium-ion) batteries. Electrodes having a higher surface area, fabricated from powdered carbon blacks, such as carbon aerogel powder, carbon aerogel microspheres, activated carbons, etc. yield high conductivity carbon compositives with excellent double layer capacity, and can be used in double layer capacitors, or for capacitive deionization and/or waste treatment of liquid streams. By adding metallic catalysts to be high surface area carbons, fuel cell electrodes can be produced.

Kaschmitter, James L. (Pleasanton, CA); Tran, Tri D. (Livermore, CA); Feikert, John H. (Livermore, CA); Mayer, Steven T. (San Leandro, CA)

1997-01-01T23:59:59.000Z

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


281

Fabricating solid carbon porous electrodes from powders  

DOE Patents (OSTI)

Fabrication is described for conductive solid porous carbon electrodes for use in batteries, double layer capacitors, fuel cells, capacitive deionization, and waste treatment. Electrodes fabricated from low surface area (<50 m{sup 2}/gm) graphite and cokes exhibit excellent reversible lithium intercalation characteristics, making them ideal for use as anodes in high voltage lithium insertion (lithium-ion) batteries. Electrodes having a higher surface area, fabricated from powdered carbon blacks, such as carbon aerogel powder, carbon aerogel microspheres, activated carbons, etc. yield high conductivity carbon composites with excellent double layer capacity, and can be used in double layer capacitors, or for capacitive deionization and/or waste treatment of liquid streams. By adding metallic catalysts to high surface area carbons, fuel cell electrodes can be produced. 1 fig.

Kaschmitter, J.L.; Tran, T.D.; Feikert, J.H.; Mayer, S.T.

1997-06-10T23:59:59.000Z

282

Performance evaluation of granular activated carbon system at Pantex: Rapid small-scale column tests to simulate removal of high explosives from contaminated groundwater  

Science Conference Proceedings (OSTI)

A granular activated carbon (GAC) system is now in operation at Pantex to treat groundwater from the perched aquifer that is contaminated with high explosives. The main chemicals of concern are RDX and HMX. The system consists of two GAC columns in series. Each column is charged with 10,000 pounds of Northwestern LB-830 GAC. At the design flow rate of 325 gpm, the hydraulic loading is 6.47 gpm/ft{sup 2}, and the empty bed contact time is 8.2 minutes per column. Currently, the system is operating at less than 10% of its design flow rate, although flow rate increases are expected in the relatively near future. This study had several objectives: Estimate the service life of the GAC now in use at Pantex; Screen several GACs to provide a recommendation on the best GAC for use at Pantex when the current GAC is exhausted and is replaced; Determine the extent to which natural organic matter in the Pantex groundwater fouls GAC adsorption sites, thereby decreasing the adsorption capacity for high explosives; and Determine if computer simulation models could match the experimental results, thereby providing another tool to follow system performance.

Henke, J.L.; Speitel, G.E. [Univ. of Texas, Austin, TX (United States). Dept. of Civil Engineering] [Univ. of Texas, Austin, TX (United States). Dept. of Civil Engineering

1998-08-01T23:59:59.000Z

283

Who lives near coke plants and oil refineries An exploration of the environmental inequity hypothesis  

SciTech Connect

Facility-specific information on pollution was obtained for 36 coke plants and 46 oil refineries in the US and matched with information on populations surrounding these 82 facilities. These data were analyzed to determine whether environmental inequities were present, whether they were more economic or racial in nature, and whether the racial composition of nearby communities has changed significantly since plants began operations. The Census tracts near coke plants have a disproportionate share of poor and nonwhite residents. Multivariate analyses suggest that existing inequities are primarily economic in nature. The findings for oil refineries are not strongly supportive of the environmental inequity hypothesis. Rank ordering of facilities by race, poverty, and pollution produces limited (although not consistent) evidence that the more risky facilities tend to be operating in communities with above-median proportions of nonwhite residents (near coke plants) and Hispanic residents (near oil refineries). Over time, the radical makeup of many communities near facilities has changed significantly, particularly in the case of coke plants sited in the early 1900s. Further risk-oriented studies of multiple manufacturing facilities in various industrial sectors of the economy are recommended.

Graham, J.D.; Beaulieu, N.D.; Sussman, D.; Sadowitz, M.; Li, Y.C. (Harvard Center for Risk Analysis, Boston, MA (United States))

1999-04-01T23:59:59.000Z

284

Coal flow aids reduce coke plant operating costs and improve production rates  

Science Conference Proceedings (OSTI)

Chemical coal flow aids can provide many benefits to coke plants, including improved production rates, reduced maintenance and lower cleaning costs. This article discusses the mechanisms by which coal flow aids function and analyzes several successful case histories. 2 refs., 10 figs., 1 tab.

Bedard, R.A.; Bradacs, D.J.; Kluck, R.W.; Roe, D.C.; Ventresca, B.P.

2005-06-01T23:59:59.000Z

285

Does EIA publish coking coal prices? - FAQ - U.S. Energy ...  

U.S. Energy Information Administration (EIA)

Search EIA.gov. A-Z Index; A-Z Index A B C D E F G H I J K L M N O P Q R S T U V W XYZ. Frequently Asked Questions. Does EIA publish coking coal ...

286

Carbon Emissions: Iron and Steel Industry  

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

Iron and Steel Industry Iron and Steel Industry Carbon Emissions in the Iron and Steel Industry The Industry at a Glance, 1994 (SIC Code: 3312) Total Energy-Related Emissions: 39.9 million metric tons of carbon (MMTC) -- Pct. of All Manufacturers: 10.7% -- Nonfuel Emissions: 22.2 MMTC Total First Use of Energy: 1,649 trillion Btu -- Pct. of All Manufacturers: 7.6% Nonfuel Use of Energy: 886 trillion Btu (53.7%) -- Coal: 858 trillion Btu (used to make coke) Carbon Intensity: 24.19 MMTC per quadrillion Btu Energy Information Administration, "1994 Manufacturing Energy Consumption Survey" and Emissions of Greenhouse Gases in the United States 1998 Energy-Related Carbon Emissions, 1994 Source of Carbon Carbon Emissions (million metric tons) All Energy Sources 39.9 Coal 22.7

287

Catalyst regeneration process including metal contaminants removal  

DOE Patents (OSTI)

Spent catalysts removed from a catalytic hydrogenation process for hydrocarbon feedstocks, and containing undesired metals contaminants deposits, are regenerated. Following solvent washing to remove process oils, the catalyst is treated either with chemicals which form sulfate or oxysulfate compounds with the metals contaminants, or with acids which remove the metal contaminants, such as 5-50 W % sulfuric acid in aqueous solution and 0-10 W % ammonium ion solutions to substantially remove the metals deposits. The acid treating occurs within the temperature range of 60.degree.-250.degree. F. for 5-120 minutes at substantially atmospheric pressure. Carbon deposits are removed from the treated catalyst by carbon burnoff at 800.degree.-900.degree. F. temperature, using 1-6 V % oxygen in an inert gas mixture, after which the regenerated catalyst can be effectively reused in the catalytic process.

Ganguli, Partha S. (Lawrenceville, NJ)

1984-01-01T23:59:59.000Z

288

METHOD OF REMOVING STRONTIUM IONS  

DOE Patents (OSTI)

A method is given for removing trace amounts of Sr/sup 90/ from solutions. Phosphate ion is added to the solution and it is then brought into contact with a solid salt such as calcium carbonate which will react methathetically with the phosphate ion to form a salt such as calcium phosphate. During this reaction, strontium will be absorbed to a high degree within the newly formed lattice. (AEC)

Rhodes, D.W.; McHenry, J.R.; Ames, L.L. Jr.

1962-05-01T23:59:59.000Z

289

Spectroscopic studies on the formation of coke on individual Fluid Catalytic Cracking particles: the effect of poisoning metal compounds.  

E-Print Network (OSTI)

??The formation of coke on individual Fluid Catalytic Cracking (FCC) catalyst particles was studied using UV/Vis microspectroscopy and confocal fluorescence microscopy, with n-hexane cracking as… (more)

Goetze, J.G.

2013-01-01T23:59:59.000Z

290

Influence of the batch's coke-ore ratio and distribution on the porosity of the melting zone  

SciTech Connect

The variation in gas permeability in the melting zone is considered as a function of the height and configuration of the coke packing and the ore component of the batch.

V.P. Tarasov; L.V. Bykov; P.V. Tarasov [Priazovsk State Technical University, Mariupol (Ukraine)

2008-09-15T23:59:59.000Z

291

Air pollution from a large steel factory: polycyclic aromatic hydrocarbon emissions from coke-oven batteries  

SciTech Connect

A systematic investigation of solid and gaseous atmospheric emissions from some coke-oven batteries of one of Europe's largest integrated steel factory (Taranto, Italy) has been carried out. These emissions, predominantly diffuse, originate from oven leakages, as well as from cyclic operations of coal loading and coke unloading. In air monitoring samples, polycyclic aromatic hydrocarbons (PAHs) were consistently detected at concentrations largely exceeding threshold limit values. By means of PAHs speciation profile and benzo-(a)pyrene (BaP) equivalent dispersion modeling from diffuse sources, the study indicated that serious health risks exist not only in working areas, but also in a densely populated residential district near the factory. 30 refs., 5 figs., 3 tabs.

Lorenzo Liberti; Michele Notarnicola; Roberto Primerano; Paolo Zannetti [Technical University of Bari, Bari (Italy). Department of Environmental Engineering and Sustainable Development

2006-03-15T23:59:59.000Z

292

Hydroprocessing Bio-oil and Products Separation for Coke Production  

Science Conference Proceedings (OSTI)

Fast pyrolysis of biomass can be used to produce a raw bio-oil product, which can be upgraded by catalytic hydroprocessing to hydrocarbon liquid products. In this study the upgraded products were distilled to recover light naphtha and oils and to produce a distillation resid with useful properties for coker processing and production of renewable, low-sulfur electrode carbon. For this hydroprocessing work, phase separation of the bio-oil was applied as a preparatory step to concentrate the heavier, more phenolic components thus generating a more amenable feedstock for resid production. Low residual oxygen content products were produced by continuous-flow, catalytic hydroprocessing of the phase separated bio-oil.

Elliott, Douglas C.; Neuenschwander, Gary G.; Hart, Todd R.

2013-04-01T23:59:59.000Z

293

Direct Conversion of Carbon Fuels in a Molten Carbonate Fuel Cell  

DOE Green Energy (OSTI)

Anodes of elemental carbon may be discharged in a galvanic cell using a molten carbonate electrolyte, a nickel-foam anode-current collector, and a porous nickel air cathode to achieve power densities of 40-100 mW/cm{sup 2}. We report cell and anode polarization, surface area, primary particle size and a crystallization index for nine particulate carbon samples derived from fuel oil, methane, coal, charred biological material and petroleum coke. At 800 C, current densities of 50-125 mA/cm{sup 2} were measured at a representative cell voltage of 0.8 V. Power densities for cells with two carbon-anode materials were found to be nearly the same on scales of 2.8- and 60 cm{sup 2} active area. Constant current operation of a small cell was accompanied by constant voltage during multiple tests of 10-30 hour duration. Cell voltage fell off after the carbon inventory was consumed. Three different cathode structures are compared, indicating that an LLNL fabricated porous nickel electrode with <10 {micro}m pores provides improved rates compared with nickel foam with 100-300 {micro}m pores. Petroleum coke containing substantial sulfur and ash discharges at a slightly lower rate than purified petroleum coke. The sulfur leads to degradation of the anode current collector over time. A conceptual model for electrochemical reactivity of carbon is presented which indicates the importance of (1) bulk lattice disorder, which continually provides surface reactive sites during anodic dissolution and (2) electrical conductivity, which lowers the ohmic component of anode polarization.

Cherepy, N J; Fiet, K J; Krueger, R; Jankowski, A F; Cooper, J F

2004-01-28T23:59:59.000Z

294

Production and screening of carbon products precursors from coal. Quarterly technical report, October 1, 1996--December 31, 1996  

Science Conference Proceedings (OSTI)

The technical work during this past quarter has focused on enhancing equipment and instrumentation in the WVU Carbon Products Laboratory. Development work on coal-based precursors for carbon foams, pitches, cokes, and fibers continues. The effects of carbon powders and chopped fibers as additives to the foam precursor are being evaluated. Extensive coordination and technology transfer activities have been undertaken and are described in Section 5 of this report.

Irwin, C.L.

1997-02-01T23:59:59.000Z

295

Usiing NovoCOS cleaning equipment in repairing the furnace-chamber lining in coke batteries 4 & 5 at OAO Koks  

SciTech Connect

Experience with a new surface-preparation technology for the ceramic resurfacing of the refractory furnace-chamber lining in coke batteries is described.

S.G. Protasov; R. Linden; A. Gross [OAO Koks, Kemerovo (Russian Federation)

2009-05-15T23:59:59.000Z

296

COST OF MERCURY REMOVAL IN IGCC PLANTS  

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

Cost of Mercury Removal Cost of Mercury Removal in an IGCC Plant Final Report September 2002 Prepared for: The United States Department of Energy National Energy Technology Laboratory By: Parsons Infrastructure and Technology Group Inc. Reading, Pennsylvania Pittsburgh, Pennsylvania DOE Product Manager: Gary J. Stiegel DOE Task Manager: James R. Longanbach Principal Investigators: Michael G. Klett Russell C. Maxwell Michael D. Rutkowski PARSONS The Cost of Mercury Removal in an IGCC Plant Final Report i September 2002 TABLE OF CONTENTS Section Title Page 1 Summary 1 2 Introduction 3 3 Background 4 3.1 Regulatory Initiatives 4 3.2 Mercury Removal for Conventional Coal-Fired Plants 4 3.3 Mercury Removal Experience in Gasification 5 3.4 Variability of Mercury Content in Coal 6 4 Design Considerations 7 4.1 Carbon Bed Location

297

Proposal of a novel multifunctional energy system for cogeneration of coke, hydrogen, and power - article no. 052001  

SciTech Connect

This paper proposes a novel multifunctional energy system (MES), which cogenerates coke, hydrogen, and power, through the use of coal and coke oven gas (COG). In this system, a new type of coke oven, firing coal instead of COG as heating resource for coking, is adopted. The COG rich in H{sub 2} is sent to a pressure swing adsorption (PSA) unit to separate about 80% of hydrogen first, and then the PSA purge gas is fed to a combined cycle as fuel. The new system combines the chemical processes and power generation system, along with the integration of chemical conversion and thermal energy utilization. In this manner, both the chemical energy of fuel and thermal energy can be used more effectively. With the same inputs of fuel and the same output of coking heat, the new system can produce about 65% more hydrogen than that of individual systems. As a result, the thermal efficiency of the new system is about 70%, and the exergy efficiency is about 66%. Compared with individual systems, the primary energy saving ratio can reach as high as 12.5%. Based on the graphical exergy analyses, we disclose that the integration of synthetic utilization of COG and coal plays a significant role in decreasing the exergy destruction of the MES system. The promising results obtained may lead to a clean coal technology that will utilize COG and coal more efficiently and economically.

Jin, H.G.; Sun, S.; Han, W.; Gao, L. [Chinese Academy of Sciences, Beijing (China)

2009-09-15T23:59:59.000Z

298

China's Industrial Carbon Dioxide Emissions in Manufacturing Subsectors and in Selected Provinces  

E-Print Network (OSTI)

for some fuels, such as coke oven gas and other gas, NBSby Fuel Fuel Type Raw Coal Cleaned Coal Washed Coal CokeCoke Oven Gas Other Gas Other Coking Products Crude Oil

Lu, Hongyou

2013-01-01T23:59:59.000Z

299

Energy efficiency and carbon dioxide emissions reduction opportunities in the U.S. Iron and Steel sector  

E-Print Network (OSTI)

constant heating of the coke ovens ensures optimization ofProgrammed heating Variable speed drive coke oven gasheating Eccentric bottom tapping (EBT) Variable speed drive on coke oven

Worrell, Ernst; Martin, N.; Price, L.

1999-01-01T23:59:59.000Z

300

Reduction of NO[sub x] emissions coke oven gas combustion process  

SciTech Connect

The paper describes by-product processing at Clairton Works which uses a unique cryogenic technology. Modifications to the desulfurization facility, nitrogen oxide formation in combustion processes (both thermal and fuel NO[sub x]), and the boilers plants are described. Boilers were used to study the contribution of fuel NO[sub x] formation during the combustion of coke oven gas. Results are summarized. The modifications made to the desulfurization facility resulted in the overall H[sub 2]S emission being reduced by 2-4 grains/100scf and the NO[sub x] emission being reduced by 21-42% in the boiler stacks.

Terza, R.R. (USS Clairton Works, PA (United States)); Sardesai, U.V. (Westfield Engineering and Services, Inc., Houston, TX (United States))

1993-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

Use of resin-bearing wastes from coke and coal chemicals production at the Novokuznetsk Metallurgical Combine  

SciTech Connect

The coke and coal chemicals plant at the Novokuznetsk Metallurgical Combine is making trial use of a technology that recycles waste products in 'tar ponds.' Specialists from the Ekomash company have installed a recycling unit in one area of the plant's dump, the unit including an inclined conveyor with a steam heater and a receiving hopper The coal preparation shop receives the wastes in a heated bin, where a screw mixes the wastes with pail of the charge for the coking ovens. The mixture subsequently travels along a moving conveyor belt together with the rest of the charge materials. The addition of up to 2% resin-bearing waste materials to the coal charge has not had any significant effect on the strength properties of the coke.

Kul'kova, T.N.; Yablochkin, N.V.; Gal'chenko, A.I.; Karyakina, E.A.; Litvinova, V.A.; Gorbach, D.A.

2007-03-15T23:59:59.000Z

302

Turbomachinery debris remover  

DOE Patents (OSTI)

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

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

1988-01-01T23:59:59.000Z

303

Process for removing thorium and recovering vanadium from titanium chlorinator waste  

DOE Patents (OSTI)

A process for removal of thorium from titanium chlorinator waste comprising: (a) leaching an anhydrous titanium chlorinator waste in water or dilute hydrochloric acid solution and filtering to separate insoluble minerals and coke fractions from soluble metal chlorides; (b) beneficiating the insoluble fractions from step (a) on shaking tables to recover recyclable or otherwise useful TiO.sub.2 minerals and coke; and (c) treating filtrate from step (a) with reagents to precipitate and remove thorium by filtration along with acid metals of Ti, Zr, Nb, and Ta by the addition of the filtrate (a), a base and a precipitant to a boiling slurry of reaction products (d); treating filtrate from step (c) with reagents to precipitate and recover an iron vanadate product by the addition of the filtrate (c), a base and an oxidizing agent to a boiling slurry of reaction products; and (e) treating filtrate from step (d) to remove any remaining cations except Na by addition of Na.sub.2 CO.sub.3 and boiling.

Olsen, Richard S. (Albany, OR); Banks, John T. (Corvallis, OR)

1996-01-01T23:59:59.000Z

304

Graphitic packing removal tool  

DOE Patents (OSTI)

Graphitic packing removal tools are described for removal of the seal rings in one piece from valves and pumps. The packing removal tool has a cylindrical base ring the same size as the packing ring with a surface finish, perforations, knurling or threads for adhesion to the seal ring. Elongated leg shanks are mounted axially along the circumferential center. A slit or slits permit insertion around shafts. A removal tool follower stabilizes the upper portion of the legs to allow a spanner wrench to be used for insertion and removal.

Meyers, K.E.; Kolsun, G.J.

1996-12-31T23:59:59.000Z

305

A new technology for producing hydrogen and adjustable ratio syngas from coke oven gas  

Science Conference Proceedings (OSTI)

About 15 billion Nm{sup 3} coke oven gas (COG) is emitted into the air in Shanxi Province in China as air pollutants. It is also a waste of precious chemical resources. In this study, COG was purified respectively by four methods including refrigeration, fiberglass, silica gel, and molecular sieve. Purified COG was separated by a prism membrane into two gas products. One consists mainly of H{sub 2} ({gt}90 vol %) and the other is rich in CH{sub 4} ({gt}60 vol %) with their exact compositions to vary with the membrane separation pressure and outlet gas flow ratio. The gas rich in CH{sub 4} was partially oxidized with oxygen in a high-temperature fixed-bed quartz reactor charged with coke particles of 10 mm size. At 1200-1300{sup o}C, a CH{sub 4} conversion of {gt}99% could be obtained. The H{sub 2}/CO ratio in the synthesis product gas can be adjusted in the range 0.3-1.4, very favorable for further C1 synthesis. 10 refs., 17 figs., 1t ab.

Jun Shen; Zhi-zhong Wang; Huai-wang Yang; Run-sheng Yao [Taiyuan University of Technology, Taiyuan (China). Department of Chemical Engineering

2007-12-15T23:59:59.000Z

306

Carbon Sequestration  

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

Technology Technology Laboratory 626 Cochrans Mill Road P.O. Box 10940 Pittsburgh, PA 15236-0940 412-386-4966 jose.figueroa@netl.doe.gov Kevin o'Brien Principal Investigator SRI International Materials Research Laboratory 333 Ravenswood Avenue Menlo Park, AK 94025 650-859-3528 kevin.obrien@sri.com Fabrication and Scale-Up oF polybenzimidazole - baSed membrane SyStem For pre - combUStion captUre oF carbon dioxide Background In order to effectively sequester carbon dioxide (CO 2 ) from a gasification plant, there must be an economically viable method for removing the CO 2 from other gases. While CO 2 separation technologies currently exist, their effectiveness is limited. Amine-based separation technologies work only at low temperatures, while pressure-swing absorption and cryogenic distillation consume significantly

307

Compacted carbon for electrochemical cells  

DOE Patents (OSTI)

This invention provides compacted carbon that is useful in the electrode of an alkali metal/carbon electrochemical cell of improved capacity selected from the group consisting of: (a) coke having the following properties: (i) an x-ray density of at least 2.00 grams per cubic centimeters, (ii) a closed porosity of no greater than 5%, and (iii) an open porosity of no greater than 47%; and (b) graphite having the following properties: (i) an x-ray density of at least 2.20 grams per cubic centimeters, (ii) a closed porosity of no greater than 5%, and (iii) an open porosity of no greater than 25%. This invention also relates to an electrode for an alkali metal/carbon electrochemical cell comprising compacted carbon as described above and a binder. This invention further provides an alkali metal/carbon electrochemical cell comprising: (a) an electrode as described above, (b) a non-aqueous electrolytic solution comprising an organic aprotic solvent and an electrolytically conductive salt and an alkali metal, and (c) a counterelectrode.

Greinke, Ronald Alfred (Medina, OH); Lewis, Irwin Charles (Strongsville, OH)

1997-01-01T23:59:59.000Z

308

Compacted carbon for electrochemical cells  

DOE Patents (OSTI)

This invention provides compacted carbon that is useful in the electrode of an alkali metal/carbon electrochemical cell of improved capacity selected from the group consisting of: (a) coke having the following properties: (1) an x-ray density of at least 2.00 grams per cubic centimeters, (2) a closed porosity of no greater than 5%, and (3) an open porosity of no greater than 47%; and (b) graphite having the following properties: (1) an x-ray density of at least 2.20 grams per cubic centimeters, (2) a closed porosity of no greater than 5%, and (3) an open porosity of no greater than 25%. This invention also relates to an electrode for an alkali metal/carbon electrochemical cell comprising compacted carbon as described above and a binder. This invention further provides an alkali metal/carbon electrochemical cell comprising: (a) an electrode as described above, (b) a non-aqueous electrolytic solution comprising an organic aprotic solvent and an electrolytically conductive salt and an alkali metal, and (c) a counter electrode. 10 figs.

Greinke, R.A.; Lewis, I.C.

1997-10-14T23:59:59.000Z

309

Delayed Coking  

U.S. Energy Information Administration (EIA)

-No Data Reported; --= Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Notes: See Definitions ...

310

Petroleum Coke  

U.S. Energy Information Administration (EIA)

-No Data Reported; --= Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Notes: Includes volumes uses as ...

311

Petroleum Coke  

Annual Energy Outlook 2012 (EIA)

88,015 81,811 82,516 82,971 84,053 85,190 1986-2012 East Coast (PADD 1) 11,973 12,198 10,887 9,316 9,766 9,003 1986-2012 Midwest (PADD 2) 15,701 15,005 15,507 16,480 16,834 17,611...

312

Urinary 1-hydroxypyrene concentrations in Chinese coke oven workers relative to job category, respirator usage, and cigarette smoking  

SciTech Connect

1-Hydroxypyrene (1-OHP) is a biomarker of recent exposure to polycyclic aromatic hydrocarbons (PAHs). We investigated whether urinary 1-OHP concentrations in Chinese coke oven workers (COWs) are modulated by job category, respirator usage, and cigarette smoking. The present cross-sectional study measured urinary 1-OHP concentrations in 197 COWs from Coking plant I and 250 COWs from Coking plant II, as well as 220 unexposed referents from Control plant I and 56 referents from Control plant II. Urinary 1-OHP concentrations (geometric mean, {mu}mol/mol creatinine) were 5.18 and 4.21 in workers from Coking plants I and II, respectively. The highest 1-OHP levels in urine were found among topside workers including lidmen, tar chasers, and whistlers. Benchmen had higher 1-OHP levels than other workers at the sideoven. Above 75% of the COWs exceeded the recommended occupational exposure limit of 2.3 {mu}mol/mol creatinine. Respirator usage and increased body mass index (BMI) slightly reduced 1-OHP levels in COWs. Cigarette smoking significantly increased urinary 1-OHP levels in unexposed referents but had no effect in COWs. Chinese COWs, especially topside workers and benchmen, are exposed to high levels of PAHs. Urinary 1-OHP concentrations appear to be modulated by respirator usage and BMI in COWs, as well as by smoking in unexposed referents.

Bo Chen; Yunping Hu; Lixing Zheng; Qiangyi Wang; Yuanfen Zhou; Taiyi Jin [Fudan University, Shanghai (China). School of Public Health

2007-09-15T23:59:59.000Z

313

PRODUCTION AND SCREENING OF CARBON PRODUCTS PRECURSORS FROM COAL  

DOE Green Energy (OSTI)

The authors have examined effects of blending a raw coal extract (EXT) with an extracted coal-tar pitch (ECTP). Previous reports were concerned with the addition of 15 wt% EXT, or less, on the physical characteristics of the blend and on the development of optical texture following carbonization. Two additional blends of ECTP and EXT were prepared at the 30 and 50 wt% EXT content using a procedure already described. The characteristics of the blends are presented. The density for these blended materials is not much different than the density for the blends reported earlier. The softening point temperature for the 30 wt% EXT increased to over 200 C while the softening point temperature for the 50 wt% EXT blend was too high to be determined by the Mettler method. Coke yields approximately follow the law of mixtures. The optical texture of the green cokes for the 30 and 50 wt% EXT blends is shown. Though the optical texture of the green cokes was not significantly affected where the level of EXT is 15 wt% or less, larger proportions of EXT exert a marked reduction in anisotropy. The co-processing of coal with petroleum residues or other heavy hydrocarbons at elevated temperature and pressure has received considerable attention in the research community as a means to upgrade simultaneously coal and byproducts. Heavy hydrocarbons can function as sources of hydrogen, as well as performing as a medium for dissolution and dispersion of coal fragments. However, the focus of much of the prior research has been on developing fuels, distillable liquids, or synthetic crudes. Comparatively little effort has been deliberately directed toward the production of heavier, non-distillable materials which could perform as binder and extender pitches, impregnants, or feedstocks for cokes and other carbons.

Caulton L. Irwin

2001-05-31T23:59:59.000Z

314

Iron Ore Sinter Produced with Charcoal Aiming Diminish the Carbon ...  

Science Conference Proceedings (OSTI)

Sources of coke are scarce and consequently the price of this fuel is increasing. Thus, this work aims at ... Economical Desulfurization of Petroleum Coke.

315

Method of recovering sulfur from the hydrogen sulfide contained in coke oven gases  

SciTech Connect

Ammonia and hydrogen sulfide are washed out of the coke oven gas and stripped from the wash liquor in the form of gases and fumes or vapors. The ammonia is decomposed in a nickel catalyzer and a small part of the decomposition gases is supplied directly to a combustion furnace, while the larger part of the combustion gases is first cooled and freed from condensate, and only then supplied to the combustion furnace. In the combustion furnace, the proportion of H/sub 2/S/SO/sub 2/ needed for the Claus process is adjusted by a partial combustion of the decomposition gases. The gases from the combustion furnace are then processed in the Claus plant to sulfur.

Laufhutte, D.

1985-04-30T23:59:59.000Z

316

Device for removing blackheads  

DOE Patents (OSTI)

A device for removing blackheads from pores in the skin having a elongated handle with a spoon shaped portion mounted on one end thereof, the spoon having multiple small holes piercing therethrough. Also covered is method for using the device to remove blackheads.

Berkovich, Tamara (116 N. Wetherly Dr., Suite 115, Los Angeles, CA)

1995-03-07T23:59:59.000Z

317

Silica Scaling Removal Process  

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

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

318

Removal of arsenic compounds from petroliferous liquids  

DOE Patents (OSTI)

Described is a process for removing arsenic from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic bound to it from contacting petroliferous liquid as described above and involves: a. treating said spent catecholated polystyrene, at a temperature in the range of about 20.degree. to 100.degree. C. with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10 and, b. separating the solids and liquids from each other. Preferably the regeneration treatment is in two steps wherein step (a) is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, steps (a) and (b) are repeated using a bicarbonate.

Fish, Richard H. (Berkeley, CA)

1985-01-01T23:59:59.000Z

319

Carbon dioxide emission index as a mean for assessing fuel quality  

Science Conference Proceedings (OSTI)

Carbon dioxide emission index, defined as the amount of CO{sub 2} released per unit of energy value, was used to rate gaseous, liquid and solid fuels. The direct utilization of natural gas is the most efficient option. The conversion of natural gas to synthesis gas for production of liquid fuels represents a significant decrease in fuel value of the former. The fuel value of liquids, such as gasoline, diesel oil, etc. is lower than that of natural gas. Blending gasoline with ethanol obtained either from bio-mass or via synthesis may decrease fuel value of the blend when CO{sub 2} emissions produced during the production of ethanol are included in total emissions. The introduction of liquid fuels produced by pyrolysis and liquefaction of biomass would result in the increase in the CO{sub 2} emissions. The CO{sub 2} emissions from the utilization of coal and petroleum coke are much higher than those from gaseous and liquid fuels. However, for petroleum coke, this is offset by the high value gaseous and liquid fuels that are simultaneously produced during coking. Conversion of low value fuels such as coal and petroleum coke to a high value chemicals via synthesis gas should be assessed as means for replacing natural gas and making it available for fuel applications.

Furimsky, E. [IMAF Group, Ottawa, ON (Canada)

2008-07-01T23:59:59.000Z

320

Continuous sulfur removal process  

DOE Patents (OSTI)

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

Jalan, V.; Ryu, J.

1994-04-26T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

IMPACCT: Carbon Capture Technology  

Science Conference Proceedings (OSTI)

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

None

2012-01-01T23:59:59.000Z

322

Removable feedwater sparger assembly  

DOE Patents (OSTI)

A removable feedwater sparger assembly includes a sparger having an inlet pipe disposed in flow communication with the outlet end of a supply pipe. A tubular coupling includes an annular band fixedly joined to the sparger inlet pipe and a plurality of fingers extending from the band which are removably joined to a retention flange extending from the supply pipe for maintaining the sparger inlet pipe in flow communication with the supply pipe. The fingers are elastically deflectable for allowing engagement of the sparger inlet pipe with the supply pipe and for disengagement therewith. 8 figs.

Challberg, R.C.

1994-10-04T23:59:59.000Z

323

Hydrogen production from simulated hot coke oven gas by using oxygen-permeable ceramics  

SciTech Connect

Hydrogen production from simulated hot coke oven gas (HCOG) was investigated in a BaCo{sub 0.7}Fe{sub 0.2}Nb{sub 0.1}O{sub 3-{delta}} (BCFNO) membrane reactor combined with a Ni/Mg(Al)O catalyst by the partial oxidation with toluene as a model tar compound under atmospheric pressure. The reaction results indicated that toluene was completely converted to H{sub 2} and CO in the catalytic reforming of the simulated HCOG in the temperature range from 825 to 875{sup o}C. Both thermodynamically predicated values and experimental data showed that the selective oxidation of toluene took precedence over that of CH{sub 4} in the reforming reaction. At optimized reaction conditions, the dense oxygen-permeable membrane has an oxygen permeation flux around 12.3 mL cm{sup -2} min{sup -1}, and a CH{sub 4} conversion of 86%, a CO{sub 2} conversion of 99%, a H{sub 2} yield of 88%, and a CO yield of 87% have been achieved. When the toluene and methane were reformed, the amount of H{sub 2} in the reaction effluent gas was about 2 times more than that of original H{sub 2} in simulated HCOG. The results reveal that it is feasible for hydrogen production from HCOG by reforming hydrocarbon compounds in a ceramic oxygen-permeable membrane reactor. 27 refs., 10 figs., 3 abs.

Hongwei Cheng; Yuwen Zhang; Xionggang Lu; Weizhong Ding; Qian Li [Shanghai University, Shanghai (China). Shanghai Key Laboratory of Modern Metallurgy and Materials Processing

2009-01-15T23:59:59.000Z

324

Non-oxidative conversion of methane with continuous hydorgen removal  

SciTech Connect

The objective is to overcome the restrictions of non-oxidative methane pyrolysis and oxidative coupling of methane by transferring hydrogen across a selective inorganic membrane between methane and air streams, without simultaneous transport of hydrocarbon reactants or products. This will make the overall reaction system exothermic, remove the thermodynamic barrier to high conversion, and eliminate the formation of carbon oxides. Our approach is to couple C-H bond activation and hydrogen removal by passage of hydrogen atoms through a dense ceramic membrane. In our membrane reactor, catalytic methane pyrolysis produces C2+ hydrogen carbons and aromatics on the one side of the membrane and hydrogen is removed through an oxide film and combusted with air on the opposite side. This process leads to a net reaction with the stoichiometry and thermodynamic properties of oxidative coupling, but without contact between the carbon atoms and oxygen species.

Borry, R.W. III [California Univ., Berkeley, CA (United States). Dept. of Chemical Engineering; Iglesia, E. [California Univ., Berkeley, CA (United States). Lawrence Berkeley Lab.

1997-12-31T23:59:59.000Z

325

Polyaniline-Based Membranes for Separating Carbon Dioxide and Methane  

Berkeley Lab researchers have optimized polymer membrane technology to more efficiently remove carbon dioxide (CO2) from natural gas. The invention ...

326

Pre-Combustion Carbon Capture Research | Department of Energy  

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

Pre-Combustion Carbon Capture Research Pre-combustion capture refers to removing CO2 from fossil fuels before combustion is completed. For example, in gasification processes a...

327

Solid materials for removing arsenic and method thereof  

Science Conference Proceedings (OSTI)

Solid materials have been developed to remove arsenic compounds from aqueous media. The arsenic is removed by passing the aqueous phase through the solid materials which can be in molded, granular, or powder form. The solid materials adsorb the arsenic leaving a purified aqueous stream. The materials are aerogels or xerogels and aerogels or xerogels and solid support structure, e.g., granulated activated carbon (GAC), mixtures. The species-specific adsorption occurs through specific chemical modifications of the solids tailored towards arsenic.

Coronado, Paul R. (Livermore, CA); Coleman, Sabre J. (Oakland, CA); Sanner, Robert D. (Livermore, CA); Dias, Victoria L. (Livermore, CA); Reynolds, John G. (San Ramon, CA)

2010-09-28T23:59:59.000Z

328

Solid materials for removing arsenic and method thereof  

DOE Patents (OSTI)

Solid materials have been developed to remove arsenic compounds from aqueous media. The arsenic is removed by passing the aqueous phase through the solid materials which can be in molded, granular, or powder form. The solid materials adsorb the arsenic leaving a purified aqueous stream. The materials are aerogels or xerogels and aerogels or xerogels and solid support structure, e.g., granulated activated carbon (GAC), mixtures. The species-specific adsorption occurs through specific chemical modifications of the solids tailored towards arsenic.

Coronado, Paul R. (Livermore, CA); Coleman, Sabre J. (Oakland, CA); Sanner, Robert D. (Livermore, CA); Dias, Victoria L. (Livermore, CA); Reynolds, John G. (San Ramon, CA)

2008-07-01T23:59:59.000Z

329

DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS  

DOE Green Energy (OSTI)

The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. The largest applications are those which support metals smelting, such as anodes for aluminum smelting and electrodes for arc furnaces. Other carbon products include materials used in creating fuels for the Direct Carbon Fuel Cell, and porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, hydrotreatment of solvent was completed in preparation for pitch fabrication for graphite electrodes. Coal digestion has lagged but is expected to be complete by next quarter. Studies are reported on coal dissolution, pitch production, foam synthesis using physical blowing agents, and alternate coking techniques.

Dady B. Dadyburjor; Mark E. Heavner; Manoj Katakdaunde; Liviu Magean; J. Joshua Maybury; Alfred H. Stiller; Joseph M. Stoffa; John W. Zondlo

2006-08-01T23:59:59.000Z

330

Sorbents for the oxidation and removal of mercury  

DOE Patents (OSTI)

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

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

2012-05-01T23:59:59.000Z

331

Sorbents for the oxidation and removal of mercury  

DOE Patents (OSTI)

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

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

2008-10-14T23:59:59.000Z

332

Improving the Carbon Dioxide Emission Estimates from the Combustion of Fossil Fuels in California  

E-Print Network (OSTI)

residual fuel oil, petroleum coke, and waste and other oil)residual fuel oil, petroleum coke, and waste and other oil22 CHP plants. For petroleum coke, CALEB only reports final

de la Rue du Can, Stephane

2010-01-01T23:59:59.000Z

333

Strategies for Low Carbon Growth In India: Industry and Non Residential Sectors  

E-Print Network (OSTI)

in the India Iron and Steel ISF Coke- Making a. b. c. d.and Stamp Charging). Maximum Recovery of Coke OvenGas Using Coke Oven Gas for achieving higher blast

Sathaye, Jayant

2011-01-01T23:59:59.000Z

334

DOE Removes Brookhaven Contractor  

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

DOE Removes DOE Removes Brookhaven Contractor Peña sends a message to DOE facilities nationwide INSIDE 2 Accelerator Rx 4 FermiKids 6 Spring at Fermilab Photos courtesy of Brookhaven National Laboratory by Judy Jackson, Office of Public Affairs Secretary of Energy Federico Peña announced on Thursday, May 1, that the Department of Energy would immediately terminate the current management contract with Associated Universities, Inc. at Brookhaven National Laboratory in Upton, New York. Peña said that he made the decision after receiving the results of a laboratory safety management review conducted by the independent oversight arm of DOE's Office of Environment, Safety and Health. In addition, the Secretary said he found unacceptable "the continued on page 8 Volume 20 Friday, May 16, 1997

335

Pneumatic soil removal tool  

DOE Patents (OSTI)

A soil removal tool is provided for removing radioactive soil, rock and other debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder mounted on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably mounted on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator valve mounted on the handle, to provide movement of the movable jaw.

Neuhaus, John E. (Newport News, VA)

1992-01-01T23:59:59.000Z

336

Pneumatic soil removal tool  

Science Conference Proceedings (OSTI)

A soil removal tool is provided for removing radioactive soil, rock and other debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder mounted on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably mounted on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator valve mounted on the handle, to provide movement of the movable jaw. 3 figs.

Neuhaus, J.E.

1992-10-13T23:59:59.000Z

337

Capturing carbon and saving coal  

SciTech Connect

Electric utilities face a tangle of choices when figuring how to pull CO{sub 2} from coal-fired plants. The article explains the three basic approaches to capturing CO{sub 2} - post-combustion, oxyfuel combustion and pre-combustion. Researchers at US DOE labs and utilities are investigating new solvents that capture CO{sub 2} more efficiently than amines and take less energy. Ammonium carbonate has been identified by EPRI as one suitable solvent. Field research projects on this are underway in the USA. Oxyfuel combustion trials are also being planned. Pre-combustion, or gasification is a completely different way of pulling energy from coal and, for electricity generation, this means IGCC systems. AEP, Southern Cinergy and Xcel are considering IGCC plants but none will capture CO{sub 2}. Rio Tinto and BP are planning a 500 MW facility to gasify coke waste from petroleum refining and collect and sequester CO{sub 2}. However, TECO recently dropped a project to build a 789 MW IGCC coal fired plant even though it was to receive a tax credit to encourage advanced coal technologies. The plant would not have captured CO{sub 2}. The company said that 'with uncertainty of carbon capture and sequestration regulations being discussed at the federal and state levels, the timing was not right'. 4 figs.

Johnson, J.

2007-10-15T23:59:59.000Z

338

Direct electrochemical conversion of carbon anode fuels in molton salt media  

DOE Green Energy (OSTI)

We are conducting research into the direct electrochemical conversion of reactive carbons into electricity--with experimental evidence of total efficiencies exceeding 80% of the heat of combustion of carbon. Together with technologies for extraction of reactive carbons from broad based fossil fuels, direct carbon conversion addresses the objectives of DOE's ''21st Century Fuel Cell'' with exceptionally high efficiency (>70% based on standard heat of reaction, {Delta}H{sub std}), as well as broader objectives of managing CO{sub 2} emissions. We are exploring the reactivity of a wide range of carbons derived from diverse sources, including pyrolyzed hydrocarbons, petroleum cokes, purified coals and biochars, and relating their electrochemical reactivity to nano/microstructural characteristics.

Cherepy, N; Krueger, R; Cooper, J F

2001-01-17T23:59:59.000Z

339

Process for removal of sulfur oxides from waste gases  

Science Conference Proceedings (OSTI)

A process for removing sulfur oxides from waste gas is provided. The gas is contacted with a sorbent selected from sodium bicarbonate, trona and activated sodium carbonate and, utilizing an alkaline liquor containing borate ion so as to reduce flow rates and loss of alkalinity, the spent sorbent is regenerated with an alkaline earth metal oxide or hydroxide.

Lowell, P.S.; Phillips, J.L.

1983-05-24T23:59:59.000Z

340

Utilization of Partially Gasified Coal for Mercury Removal  

Science Conference Proceedings (OSTI)

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

Chris Samuelson; Peter Maly; David Moyeda

2008-09-09T23:59:59.000Z

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


341

Cyclic process for producing methane in a tubular reactor with effective heat removal  

DOE Patents (OSTI)

Carbon monoxide-containing gas streams are converted to methane by a cyclic, essentially two-step process in which said carbon monoxide is disproportionated to form carbon dioxide and active surface carbon deposited on the surface of a catalyst, and said carbon is reacted with steam to form product methane and by-product carbon dioxide. The exothermic heat of reaction generated in each step is effectively removed during each complete cycle so as to avoid a build up of heat from cycle-to-cycle, with particularly advantageous techniques being employed for fixed bed, tubular and fluidized bed reactor operations.

Frost, Albert C. (Congers, NY); Yang, Chang-Lee (Spring Valley, NY)

1986-01-01T23:59:59.000Z

342

Engine Removal Projection Tool  

DOE Green Energy (OSTI)

The US Navy has over 3500 gas turbine engines used throughout the surface fleet for propulsion and the generation of electrical power. Past data is used to forecast the number of engine removals for the next ten years and determine engine down times between removals. Currently this is done via a FORTRAN program created in the early 1970s. This paper presents results of R&D associated with creating a new algorithm and software program. We tested over 60 techniques on data spanning 20 years from over 3100 engines and 120 ships. Investigated techniques for the forecast basis including moving averages, empirical negative binomial, generalized linear models, Cox regression, and Kaplan Meier survival curves, most of which are documented in engineering, medical and scientific research literature. We applied those techniques to the data, and chose the best algorithm based on its performance on real-world data. The software uses the best algorithm in combination with user-friendly interfaces and intuitively understandable displays. The user can select a specific engine type, forecast time period, and op-tempo. Graphical displays and numerical tables present forecasts and uncertainty intervals. The technology developed for the project is applicable to other logistic forecasting challenges.

Ferryman, Thomas A.; Matzke, Brett D.; Wilson, John E.; Sharp, Julia L.; Greitzer, Frank L.

2005-06-02T23:59:59.000Z

343

CARBON-CARBON COMPOSITE ALLCOMP Carbon-Carbon Composite  

E-Print Network (OSTI)

strength 4340 steel, carbon-carbon composite, and Carbon-Silicon Carbide composite were tested to examine-C composite containing continuous PAN T300 fibers · SWB: Chopped Fiber Composite containing SWB fibers Crush

Rollins, Andrew M.

344

Agricultural Carbon Mitigation in Europe  

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

Agricultural Carbon Mitigation in Europe Agricultural Carbon Mitigation in Europe Agricultural Carbon Mitigation in Europe Smith P, Powlson DS, Smith JU, Falloon P, and Coleman K. 2000. Meeting Europe's climate change commitments: Quantitative estimates of the potential for carbon mitigation by agriculture. Global Climate Change 6:525-539. Abstract Under the Kyoto Protocol, the European Union is committed to a reduction in CO2 emissions to 92% of baseline (1990) levels during the first commitment period (2008-2012). The Kyoto Protocol allows carbon emissions to be offset by demonstrable removal of carbon from the atmosphere. Thus, land-use / land-management change and forestry activities that are shown to reduce atmospheric CO2 levels can be included in the Kyoto targets. These activities include afforestation, reforestation and deforestation (article

345

Removal of arsenic compounds from petroliferous liquids  

DOE Patents (OSTI)

The present invention in one aspect comprises a process for removing arsenic from petroliferous-derived liquids by contacting said liquid with a divinylbenzene-crosslinked polystyrene polymer (i.e. PS-DVB) having catechol ligands anchored to said polymer, said contacting being at an elevated temperature. In another aspect, the invention is a process for regenerating spent catecholated polystyrene polymer by removal of the arsenic bound to it from contacting petroliferous liquid in accordance with the aspect described above which regenerating process comprises: (a) treating said spent catecholated polystyrene polymer with an aqueous solution of at least one member selected from the group consisting of carbonates and bicarbonates of ammonium, alkali metals, and alkaline earth metals, said solution having a pH between about 8 and 10, and said treating being at a temperature in the range of about 20/sup 0/ to 100/sup 0/C; (b) separating the solids and liquids from each other. In a preferred embodiment the regeneration treatment is in two steps wherein step: (a) is carried out with an aqueous alcoholic carbonate solution which includes at least one lower alkyl alcohol, and, steps (c) and (d) are added. Steps (c) and (d) comprise: (c) treating the solids with an aqueous alcoholic solution of at least one ammonium, alkali or alkaline earth metal bicarbonate at a temperature in the range of about 20 to 100/sup 0/C; and (d) separating the solids from the liquids.

Fish, R.H.

1984-04-06T23:59:59.000Z

346

Geothermal hydrogen sulfide removal  

DOE Green Energy (OSTI)

UOP Sulfox technology successfully removed 500 ppM hydrogen sulfide from simulated mixed phase geothermal waters. The Sulfox process involves air oxidation of hydrogen sulfide using a fixed catalyst bed. The catalyst activity remained stable throughout the life of the program. The product stream composition was selected by controlling pH; low pH favored elemental sulfur, while high pH favored water soluble sulfate and thiosulfate. Operation with liquid water present assured full catalytic activity. Dissolved salts reduced catalyst activity somewhat. Application of Sulfox technology to geothermal waters resulted in a straightforward process. There were no requirements for auxiliary processes such as a chemical plant. Application of the process to various types of geothermal waters is discussed and plans for a field test pilot plant and a schedule for commercialization are outlined.

Urban, P.

1981-04-01T23:59:59.000Z

347

Pneumatic soil removal tool  

Science Conference Proceedings (OSTI)

A soil tool is provided for removing radioactive soil, rock and debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator value mounted on the handle, to provide movement of the movable jaw.

Neuhaus, J.F.

1991-01-23T23:59:59.000Z

348

Forming foam structures with carbon foam substrates  

Science Conference Proceedings (OSTI)

The invention provides foams of desired cell sizes formed from metal or ceramic materials that coat the surfaces of carbon foams which are subsequently removed. For example, metal is located over a sol-gel foam monolith. The metal is melted to produce a metal/sol-gel composition. The sol-gel foam monolith is removed, leaving a metal foam.

Landingham, Richard L.; Satcher, Jr., Joe H.; Coronado, Paul R.; Baumann, Theodore F.

2012-11-06T23:59:59.000Z

349

DOE Manual Studies Terrestrial Carbon Sequestration | Department of Energy  

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

Manual Studies Terrestrial Carbon Sequestration Manual Studies Terrestrial Carbon Sequestration DOE Manual Studies Terrestrial Carbon Sequestration January 18, 2011 - 12:00pm Addthis Washington, DC - There is considerable opportunity and growing technical sophistication to make terrestrial carbon sequestration both practical and effective, according to the latest carbon capture and storage (CCS) "best practices" manual issued by the U.S. Department of Energy. Best Practices for Terrestrial Sequestration of Carbon Dioxide details the most suitable operational approaches and techniques for terrestrial sequestration, a carbon dioxide (CO2) mitigation strategy capable of removing CO2 already in the air. Consequently, terrestrial sequestration, which uses photosynthesis - part of the natural carbon cycle - to create

350

Nitrogen Removal From Low Quality Natural Gas  

SciTech Connect

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

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

1997-10-01T23:59:59.000Z

351

Ab Initio Studies of Coke Formation on Ni Catalysts During Methane Reforming  

SciTech Connect

The atomic-scale processes that control the formation of carbon deposits on Ni catalysts in reforming applications are poorly understood. Ab initio Density Functional Theory calculations have been used to examine several key elementary steps in the complex network of chemical reactions that precedes carbon formation on practical catalysts. Attention has been focused on the disproportionation of CO. A comparative study of this reaction on flat and stepped crystal planes of Ni has provided the first direct evidence that surface carbon formation is driven by elementary reactions occurring at defect sites on Ni catalysts. The adsorption and diffusion of atomic H on several flat and stepped Ni surfaces has also been characterized experimentally.

David S. Sholl

2006-03-05T23:59:59.000Z

352

AB INITIO STUDIES OF COKE FORMATION ON NI CATALYSTS DURING METHANE REFORMING  

SciTech Connect

The atomic-scale processes that control the formation of carbon deposits on Ni catalysts in reforming applications are poorly understood. Ab initio Density Functional Theory calculations have been used to examine several key elementary steps in the complex network of chemical reactions that precedes carbon formation on practical catalysts. Attention has been focused on the disproportionation of CO. A comparative study of this reaction on flat and stepped crystal planes of Ni has provided the first direct evidence that surface carbon formation is driven by elementary reactions occurring at defect sites on Ni catalysts. The adsorption and diffusion of atomic H on several flat and stepped Ni surfaces has also been characterized experimentally.

David S. Sholl

2004-09-25T23:59:59.000Z

353

,,,,,,"Coal Components",,,"Coke",,,"Electricity Components",,,,,,,,,,,,,,"Natural Gas Components",,,"Steam Components"  

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

2 Relative Standard Errors for Table 7.2;" 2 Relative Standard Errors for Table 7.2;" " Unit: Percents." ,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,"Selected Wood and Other Biomass Components" ,,,,,,"Coal Components",,,"Coke",,,"Electricity Components",,,,,,,,,,,,,,"Natural Gas Components",,,"Steam Components" " "," ",,,,,,,,,,,,,"Total",,,,,,,,,,,,,,,,,,,,,,,"Wood Residues",,,," " " "," "," ",,,,,"Bituminous",,,,,,"Electricity","Diesel Fuel",,,,,,"Motor",,,,,,,"Natural Gas",,,"Steam",,,," ",,,"and","Wood-Related","All"

354

Development of a mathematical description of catalytic reforming taking into account changes of the individual components of the feedstock and catalyst coking  

Science Conference Proceedings (OSTI)

This paper presents an approach for modeling petroleum and petrochemical processing. Based on this approach a mathematical model has been developed for catalytic reforming taking into account changes of individual feedstock components and catalyst coking. Examples are given of calculations and optimization of industrial equipment.

Rabinovich, G.B.; Dynkina, N.E.

1985-12-01T23:59:59.000Z

355

,,,,,,"Coal Components",,,"Coke",,,"Electricity Components",,,,,,,,,,,,,,"Natural Gas Components",,,"Steam Components"  

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

Relative Standard Errors for Table 7.1;" Relative Standard Errors for Table 7.1;" " Unit: Percents." ,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,"Selected Wood and Other Biomass Components" ,,,,,,"Coal Components",,,"Coke",,,"Electricity Components",,,,,,,,,,,,,,"Natural Gas Components",,,"Steam Components" " "," ",,,,,,,,,,,,,"Total",,,,,,,,,,,,,,,,,,,,,,,"Wood Residues",,,," " " "," "," ",,,,,"Bituminous",,,,,,"Electricity","Diesel Fuel",,,,,,"Motor",,,,,,,"Natural Gas",,,"Steam",,,," ",,,"and","Wood-Related","All"

356

CARBON TETRACHLORIDE  

E-Print Network (OSTI)

This fact sheet answers the most frequently asked health questions (FAQs) about carbon tetrachloride.

unknown authors

2005-01-01T23:59:59.000Z

357

DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS  

DOE Green Energy (OSTI)

This NETL sponsored effort seeks to develop continuous technologies for the production of carbon products, which may be thought of as the heavier products currently produced from refining of crude petroleum and coal tars obtained from metallurgical grade coke ovens. This effort took binder grade pitch, produced from liquefaction of West Virginia bituminous grade coal, all the way to commercial demonstration in a state of the art arc furnace. Other products, such as crude oil, anode grade coke and metallurgical grade coke were demonstrated successfully at the bench scale. The technology developed herein diverged from the previous state of the art in direct liquefaction (also referred to as the Bergius process), in two major respects. First, direct liquefaction was accomplished with less than a percent of hydrogen per unit mass of product, or about 3 pound per barrel or less. By contrast, other variants of the Bergius process require the use of 15 pounds or more of hydrogen per barrel, resulting in an inherent materials cost. Second, the conventional Bergius process requires high pressure, in the range of 1500 psig to 3000 psig. The WVU process variant has been carried out at pressures below 400 psig, a significant difference. Thanks mainly to DOE sponsorship, the WVU process has been licensed to a Canadian Company, Quantex Energy Inc, with a commercial demonstration unit plant scheduled to be erected in 2011.

Elliot Kennel; Chong Chen; Dady Dadyburjor; Mark Heavner; Manoj Katakdaunde; Liviu Magean; James Mayberry; Alfred Stiller; Joseph Stoffa; Christopher Yurchick; John Zondlo

2009-12-31T23:59:59.000Z

358

Carbon dioxide capture process with regenerable sorbents  

DOE Patents (OSTI)

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

Pennline, Henry W. (Bethel Park, PA); Hoffman, James S. (Library, PA)

2002-05-14T23:59:59.000Z

359

NETL: Carbon Storage  

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

Carbon Sequestration Partnerships Regional Carbon Sequestration Partnership (RCSP) Programmatic Points of Contact Carbon Storage Program Infrastructure Coordinator Carbon Storage...

360

Removal to Maximum Extent Practical  

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

Summary Notes from 1 November 2007 Generic Technical Issue Discussion on Removal of Highly Radioactive Radionuclides/Key Radionuclides to the Maximum Extent Practical

Note: This page contains sample records for the topic "remove carbon coke" 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

Influence of technological factors on statics of hydrogen sulfide absorption from coke-oven gas by the ammonia process  

SciTech Connect

The basic technological factors that determine the effectiveness of hydrogen sulfide absorption from coke-oven gas by the cyclic ammonia process are the initial H/sub 2/S content of the gas, the degree of purification, the absorption temperature and the NH/sub 3/ and CO/sub 2/ contents of the absorbent solution. The effects of these factors on the statics of hydrogen sulfide absorption are studied. The investigation is based on the phase-equilibrium distributions of components in the absorption-desorption gas-cleaning cycle. The mathematical model is presented which includes the solution of a system of chemical equilibrium equations for reactions in the solution, material balances, and electrical neutrality. 4 references, 5 figures, 1 table.

Nazarov, V.G.; Kamennykh, B.M.; Rus'yanov, N.D.

1983-01-01T23:59:59.000Z

362

Executive summary: Technical and economic feasibility study. Trigeneration project, Shanghai Coking and Chemical Plant. Export trade information  

SciTech Connect

The study, conducted by Bechtel, Inc., was funded by the U.S. Trade and Development Agency. The purpose of the study is to assess the feasibility of establishing a new coal-based Trigeneration Complex as an addition to the existing Shanghai Coking and Chemical Plant. The complex would produce gas for the city of Shanghai, chemicals for domestic consumption and foreign export, and utilities for use within the complex and for export to other facilities. The report presents an in-depth study of the economic and technical aspects of the project, as well as an outline of project implementation phases. The study is divided into the following sections: (1) Introduction; (2) Summary; (3) Study Bases; (4) Process Selection and Rationale; (5) Chemical Selection and Marketing; (6) Definition of Facilities; (7) Site and Plot Plan.

NONE

1987-01-01T23:59:59.000Z

363

SEPARATION OF HEAVY METALS: REMOVAL FROM INDUSTRIAL WASTEWATERS  

Office of Scientific and Technical Information (OSTI)

SEPARATION SEPARATION OF HEAVY METALS: REMOVAL FROM INDUSTRIAL WASTEWATERS AND CONTAMINATED SOIL* Robert W. Peters + and Linda Shem Energy Systems Division Argonne National Laboratory 9700 South Cass Avenue Argonne, Illinois 60439 Abstract This paper reviews the applicable separation technologies relating to removal of heavy metals from solution and from soils in order to present the state-of-the-art in the field. Each technology is briefly described and typical operating conditions and technology performance are presented. Technologies described include chemical precipitation (including hydroxide, carbonate, or sulfide reagents), coagulation/flocculation, ion exchange, solvent extraction, extraction with chelating agents, complexation, electrochemical operation, cementation, membrane operations, evaporation, adsorption, solidification/stabilization, and

364

Energy Savings for CO2 Removal in Ammonia Plants  

E-Print Network (OSTI)

An exergy analysis of carbonate solution C02 removal systems which use solution flashing shows that there is no energy saving by using a mechanical thermocompressor instead of a steam-jet ejector. In a 1000 ShT/D ammonia plant an energy saving of approx. 27 GJ/h (GHV) of natural gas is possible by using exhaust steam from a back pressure turbine instead of L.T. shift gas as the heat supply source for a Carsol C02 removal system.

Pouilliart, R.; Van Hecke, F. C.

1981-01-01T23:59:59.000Z

365

Ozone Removal by Filters Containing Activated Carbon: A Pilot Study  

E-Print Network (OSTI)

organic compounds. IAQ'92, ASHRAE, Atlanta: 233-241.Indoor Air 18(2): 156-70. ASHRAE (1992). Gravimetric andparticulate matter. ANSI/ASHRAE standard 52.1-1992 Atlanta,

Fisk, William

2012-01-01T23:59:59.000Z

366

Carbon Nanotube Membranes: Carbon Nanotube Membranes for Energy-Efficient Carbon Sequestration  

SciTech Connect

Broad Funding Opportunity Announcement Project: Porifera is developing carbon nanotube membranes that allow more efficient removal of CO2 from coal plant exhaust. Most of today’s carbon capture methods use chemical solvents, but capture methods that use membranes to draw CO2 out of exhaust gas are potentially more efficient and cost effective. Traditionally, membranes are limited by the rate at which they allow gas to flow through them and the amount of CO2 they can attract from the gas. Smooth support pores and the unique structure of Porifera’s carbon nanotube membranes allows them to be more permeable than other polymeric membranes, yet still selective enough for CO2 removal. This approach could overcome the barriers facing membrane-based approaches for capturing CO2 from coal plant exhausts.

None

2010-03-01T23:59:59.000Z

367

Bead and Process for Removing Dissolved Metal Contaminants  

DOE Patents (OSTI)

A bead is provided which comprises or consists essentially of activated carbon immobilized by crosslinked poly (carboxylic acid) binder, sodium silicate binder, or polyamine binder. The bead is effective to remove metal and other ionic contaminants from dilute aqueous solutions. A method of making metal-ion sorbing beads is provided, comprising combining activated carbon, and binder solution (preferably in a pin mixer where it is whipped), forming wet beads, and heating and drying the beads. The binder solution is preferably poly(acrylic acid) and glycerol dissolved in water and the wet beads formed from such binder solution are preferably heated and crosslinked in a convection oven.

Summers, Bobby L., Jr.; Bennett, Karen L.; Foster, Scott A.

2005-01-18T23:59:59.000Z

368

It's Elemental - The Element Carbon  

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

it does occur naturally, most commercial graphite is produced by treating petroleum coke, a black tar residue remaining after the refinement of crude oil, in an oxygen-free...

369

"1. Carbon Dioxide Emission Factors for Stationary Combustion1"  

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

Fuel Emission Factors" Fuel Emission Factors" "(From Appendix H of the instructions to Form EIA-1605)" "1. Carbon Dioxide Emission Factors for Stationary Combustion1" "Fuel ",,"Emission Factor ",,"Units" "Coal2" "Anthracite",,103.69,,"kg CO2 / MMBtu" "Bituminous",,93.28,,"kg CO2 / MMBtu" "Sub-bituminous",,97.17,,"kg CO2 / MMBtu" "Lignite",,97.72,,"kg CO2 / MMBtu" "Electric Power Sector",,95.52,,"kg CO2 / MMBtu" "Industrial Coking",,93.71,,"kg CO2 / MMBtu" "Other Industrial",,93.98,,"kg CO2 / MMBtu" "Residential/Commercial",,95.35,,"kg CO2 / MMBtu" "Natural Gas3"

370

Failing Drop CO2 Deposition (Desublimation) Heat Exchanger for the Cryogenic Carbon Capture Process.  

E-Print Network (OSTI)

??Cryogenic carbon capture removes CO2 and other pollutants from flue and waste stream gases produced from the combustion of fossil fuels such as coal, natural… (more)

James, David William

2011-01-01T23:59:59.000Z

371

NETL: Carbon Sequestration Atlas of the U.S. and Canada  

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

the first and second editions of the United States Carbon Utilization and Storage Atlas (Atlas I and Atlas II, respectively) have been removed from the NETL website. Atlas...

372

CRBRP decay heat removal systems  

SciTech Connect

The Decay Heat Removal Systems for the Clinch River Breeder Reactor Plant (CRBRP) are designed to adequately remove sensible and decay heat from the reactor following normal shutdown, operational occurrences, and postulated accidents on both a short term and a long term basis. The Decay Heat Removal Systems are composed of the Main Heat Transport System, the Main Condenser and Feedwater System, the Steam Generator Auxiliary Heat Removal System (SGAHRS), and the Direct Heat Removal Service (DHRS). The overall design of the CRBRP Decay Heat Removal Systems and the operation under normal and off-normal conditions is examined. The redundancies of the system design, such as the four decay heat removal paths, the emergency diesel power supplies, and the auxiliary feedwater pumps, and the diversities of the design such as forced circulation/natural circulation and AC Power/DC Power are presented. In addition to overall design and system capabilities, the detailed designs for the Protected Air Cooled Condensers (PACC) and the Air Blast Heat Exchangers (ABHX) are presented.

Hottel, R.E.; Louison, R.; Boardman, C.E.; Kiley, M.J.

1977-01-01T23:59:59.000Z

373

Removal of arsenic compounds from spent catecholated polymer  

DOE Patents (OSTI)

Described is a process for removing arsenic from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic bound to it from contacting petroliferous liquid as described above and involves: a. treating said spent catecholated polystyrene, at a temperature in the range of about 20.degree. to 100.degree. C. with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10 and, b. separating the solids and liquids from each other. Preferably the regeneration treatment is in two steps wherein step (a) is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, steps (a) and (b) are repeated using a bicarbonate.

Fish, Richard H. (Berkeley, CA)

1985-01-01T23:59:59.000Z

374

Carbon Cycle  

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

Carbon Cycle Carbon Cycle Latest Global Carbon Budget Estimates Including CDIAC Estimates Terrestrial Carbon Management Data Sets and Analyses Carbon Dioxide Emissions from Fossil-Fuel Consumption and Cement Manufacture, (2011) Annual Fossil-Fuel CO2 Emissions: Mass of Emissions Gridded by One Degree Latitude by One Degree Longitude (2012) Monthly Fossil-Fuel CO2 Emissions: Mass of Emissions Gridded by One Degree Latitude by One Degree Longitude (2012) Annual Fossil-Fuel CO2 Emissions: Global Stable Carbon Isotopic Signature (2012) Monthly Fossil-Fuel CO2 Emissions: Isomass (δ 13C) of Emissions Gridded by One Degree Latitude by One Degree Longitude (2012) AmeriFlux - Terrestrial Carbon Dioxide, Water Vapor, and Energy Balance Measurements Estimates of Monthly CO2 Emissions and Associated 13C/12C Values

375

Carbon Isotopes  

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

Atmospheric Trace Gases » Carbon Isotopes Atmospheric Trace Gases » Carbon Isotopes Carbon Isotopes Gateway Pages to Isotopes Data Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and Carbon-13 in Methane 800,000 Deuterium Record and Shorter Records of Various Isotopic Species from Ice Cores Carbon-13 13C in CO Measurements from Niwot Ridge, Colorado and Montana de Oro, California (Tyler) 13C in CO2 NOAA/CMDL Flask Network (White and Vaughn) CSIRO GASLAB Flask Network (Allison, Francey, and Krummel) CSIRO in situ measurements at Cape Grim, Tasmania (Francey and Allison) Scripps Institution of Oceanography (Keeling et al.) 13C in CH4 NOAA/CMDL Flask Network (Miller and White) Northern & Southern Hemisphere Sites (Quay and Stutsman) Northern & Southern Hemisphere Sites (Stevens)

376

Metal chelate process to remove pollutants from fluids  

DOE Patents (OSTI)

The present invention relates to improved methods using an organic iron chelate to remove pollutants from fluids, such as flue gas. Specifically, the present invention relates to a process to remove NO[sub x] and optionally SO[sub 2] from a fluid using a metal ion (Fe[sup 2+]) chelate wherein the ligand is a dimercapto compound wherein the --SH groups are attached to adjacent carbon atoms (HS--C--C--SH) or (SH--C--CCSH) and contain a polar functional group so that the ligand of DMC chelate is water soluble. Alternatively, the DMC is covalently attached to a water insoluble substrate such as a polymer or resin, e.g., polystyrene. The chelate is regenerated using electroreduction or a chemical additive. The dimercapto compound bonded to a water insoluble substrate is also useful to lower the concentration or remove hazardous metal ions from an aqueous solution. 26 figures.

Chang, S.G.T.

1994-12-06T23:59:59.000Z

377

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

378

Further investigation of the impact of the co-combustion of tire-derived fuel and petroleum coke on the petrology and chemistry of coal combustion products  

Science Conference Proceedings (OSTI)

A Kentucky cyclone-fired unit burns coal and tire-derived fuel, sometimes in combination with petroleum coke. A parallel pulverized combustion (pc) unit at the same plant burns the same coal, without the added fuels. The petrology, chemistry, and sulfur isotope distribution in the fuel and resulting combustion products was investigated for several configurations of the fuel blend. Zinc and Cd in the combustion products are primarily contributed from the tire-derived fuel, the V and Ni are primarily from the petroleum coke, and the As and Hg are probably largely from the coal. The sulfur isotope distribution in the cyclone unit is complicated due to the varying fuel sources. The electrostatic precipitator (ESP) array in the pc unit shows a subtle trend towards heavier S isotopic ratios in the cooler end of the ESP.

Hower, J.C.; Robertson, J.D.; Elswick, E.R.; Roberts, J.M.; Brandsteder, K.; Trimble, A.S.; Mardon, S.M. [University of Kentucky, Lexington, KY (United States). Center for Applied Energy Research

2007-07-01T23:59:59.000Z

379

Article removal device for glovebox  

DOE Patents (OSTI)

An article removal device for a glovebox is described comprising a conduit extending through a glovebox wall which may be closed by a plug within the glovebox, and a fire-resistant container closing the outer end of the conduit and housing a removable container for receiving pyrophoric or otherwise hazardous material without disturbing the interior environment of the glovebox or adversely affecting the environment outside of the glovebox. (Official Gazette)

Guyer, R.H.; Leebl, R.G.

1973-12-01T23:59:59.000Z

380

Biofuels Science and Facilities (Carbon Cycle 2.0)  

DOE Green Energy (OSTI)

Jay D. Keasling speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/

Keasling, Jay D.

2010-02-04T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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

A Multi-Factor Analysis of Sustainable Agricultural Residue Removal Potential  

Science Conference Proceedings (OSTI)

Agricultural residues have significant potential as a near term source of cellulosic biomass for bioenergy production, but sustainable removal of agricultural residues requires consideration of the critical roles that residues play in the agronomic system. Previous work has developed an integrated model to evaluate sustainable agricultural residue removal potential considering soil erosion, soil organic carbon, greenhouse gas emission, and long-term yield impacts of residue removal practices. The integrated model couples the environmental process models WEPS, RUSLE2, SCI, and DAYCENT. This study uses the integrated model to investigate the impact of interval removal practices in Boone County, Iowa, US. Residue removal of 4.5 Mg/ha was performed annually, bi-annually, and tri-annually and were compared to no residue removal. The study is performed at the soil type scale using a national soil survey database assuming a continuous corn rotation with reduced tillage. Results are aggregated across soil types to provide county level estimates of soil organic carbon changes and individual soil type soil organic matter content if interval residue removal were implemented. Results show interval residue removal is possible while improving soil organic matter. Implementation of interval removal practices provide greater increases in soil organic matter while still providing substantial residue for bioenergy production.

Jared Abodeely; David Muth; Paul Adler; Eleanor Campbell; Kenneth Mark Bryden

2012-10-01T23:59:59.000Z

382

Effects of polymerization and briquetting parameters on the tensile strength of briquettes formed from coal coke and aniline-formaldehyde resin  

SciTech Connect

In this work, the utilization of aniline (C{sub 6}H{sub 7}N) formaldehyde (HCHO) resins as a binding agent of coke briquetting was investigated. Aniline (AN) formaldehyde (F) resins are a family of thermoplastics synthesized by condensing AN and F in an acid solution exhibiting high dielectric strength. The tensile strength sharply increases as the ratio of F to AN from 0.5 to 1.6, and it reaches the highest values between 1.6 and 2.2 F/AN ratio; it then slightly decreases. The highest tensile strength of F-AN resin-coke briquette (23.66 MN/m{sup 2}) was obtained from the run with 1.5 of F/AN ratio by using (NH4){sub 2}S{sub 2}O{sub 8} catalyst at 310 K briquetting temperature. The tensile strength of F-AN resin-coke briquette slightly decreased with increasing the catalyst percent to 0.10%, and then it sharply decreased to zero with increasing the catalyst percent to 0.2%. The effect of pH on the tensile strength is irregular. As the pH of the mixture increases from 9.0 to 9.2, the tensile strength shows a sharp increase, and the curve reaches a plateau value between pH 9.3 and 9.9; then the tensile strength shows a slight increase after pH = 9.9.

Demirbas, A.; Simsek, T. [Selcuk University, Konya (Turkey)

2006-10-15T23:59:59.000Z

383

Soil organic carbon – A Western Australian perspective Soil organic carbon A Western Australian perspective  

E-Print Network (OSTI)

Sequestering carbon in soils is being investigated worldwide as a way to remove carbon dioxide from the atmosphere and provide land managers with extra income from the sale of carbon offsets or credits. In theory, the opportunity exists for farmers and other land managers to be paid via voluntary trades or carbon trading schemes to implement land management changes that sequester soil carbon, with additional benefits gained in improving the biological, chemical and physical health of their soils. The concept of increasing soil organic carbon is very attractive because it seemingly provides a ‘win-win’ situation in which farmers earn extra income for removing greenhouse gas emissions from the atmosphere while simultaneously lifting the productivity of arable soils. But how realistic is this concept and what opportunities and risks does it present to farmers? Soil organic carbon is part of the global carbon cycle The soil can either represent an enormous ‘source’ or ‘sink ’ of carbon – with more carbon contained in the soil than in the world’s vegetation and atmosphere combined. Soil organic carbon represents a critical component

Janet Paterson; Dr. Fran Hoyle; Department Of Agriculture

2011-01-01T23:59:59.000Z

384

Method for removing cesium from a nuclear reactor coolant  

DOE Patents (OSTI)

A method of and system for removing cesium from a liquid metal reactor coolant including a carbon packing trap in the primary coolant system for absorbing a major portion of the radioactive cesium from the coolant flowing therethrough at a reduced temperature. A regeneration subloop system having a secondary carbon packing trap is selectively connected to the primary system for isolating the main trap therefrom and connecting it to the regeneration system. Increasing the temperature of the sodium flowing through the primary trap diffuses a portion of the cesium inventory thereof further into the carbon matrix while simultaneously redispersing a portion into the regeneration system for absorption at a reduced temperature by the secondary trap.

Colburn, R.P.

1983-08-10T23:59:59.000Z

385

High removal rate laser-based coating removal system  

DOE Patents (OSTI)

A compact laser system that removes surface coatings (such as paint, dirt, etc.) at a removal rate as high as 1000 ft.sup.2 /hr or more without damaging the surface. A high repetition rate laser with multiple amplification passes propagating through at least one optical amplifier is used, along with a delivery system consisting of a telescoping and articulating tube which also contains an evacuation system for simultaneously sweeping up the debris produced in the process. The amplified beam can be converted to an output beam by passively switching the polarization of at least one amplified beam. The system also has a personal safety system which protects against accidental exposures.

Matthews, Dennis L. (Moss Beach, CA); Celliers, Peter M. (Berkeley, CA); Hackel, Lloyd (Livermore, CA); Da Silva, Luiz B. (Danville, CA); Dane, C. Brent (Livermore, CA); Mrowka, Stanley (Richmond, CA)

1999-11-16T23:59:59.000Z

386

Irradiation Stability of Carbon Nanotubes  

E-Print Network (OSTI)

Ion irradiation of carbon nanotubes is a tool that can be used to achieve modification of the structure. Irradiation stability of carbon nanotubes was studied by ion and electron bombardment of the samples. Different ion species at various energies were used in experiments, and several defect characterization techniques were applied to characterize the damage. Development of dimensional changes of carbon nanotubes in microscopes operated at accelerating voltages of 30 keV revealed that binding energy of carbon atoms in CNs is much lower than in bulk materials. Resistivity measurements during irradiation demonstrated existence of a quasi state of defect creation. Linear relationship between ID/IG ratio and increasing irradiation fluence was revealed by Raman spectroscopy study of irradiated carbon buckypapers. The deviations from linear relationship were observed for the samples irradiated to very high fluence values. Annealing of irradiated samples was able to reduce the value of ID/IG ratio and remove defects. However, annealing could not affect ID/IG ratio and remove defects in amorphized samples. The extracted value of activation energy for irradiated sample was 0.36 ±0.05 eV. The value of activation energy was in good agreement with theoretical studies.

Aitkaliyeva, Assel

2009-08-01T23:59:59.000Z

387

Carbon Nanotubes  

Science Conference Proceedings (OSTI)

Carbon Nanotubes. Sponsored by: TMS Electronic, Magnetic and Photonic Materials Division Date and Time: Sunday, February 13, 2005 ~ 8:30 am-5:00 pm

388

Carbon Nanomaterials  

Science Conference Proceedings (OSTI)

Mar 12, 2012 ... The graphene film was spin-coated using carbon nanotubes to form the cathode of the field emission device. A phosphor coated graphene-PET ...

389

Removal - An alternative to clearance  

SciTech Connect

This presentation shows the differences between the application of clearance and removal, both being procedures for materials leaving radiation protection areas permanently. The differentiation will be done on the basis of the German legislation but may be also applicable for other national legislation. For clearance in Germany two basic requirements must be given, i.e. that the materials are activated or contaminated and that they result from the licensed use or can be assigned to the scope of the license. Clearance needs not to be applied to objects in Germany which are to be removed only temporarily from controlled areas with the purpose of repair or reuse in other controlled areas. In these cases only the requirements of contamination control apply. In the case of removal it must either be proved by measurements that the relevant materials are neither activated nor contaminated or that the materials result from areas where activation or contamination is impossible due to the operational history considering operational procedures and events. If the material is considered neither activated nor contaminated there is no need for a clearance procedure. Therefore, these materials can be removed from radiation protection areas and the removal is in the responsibility of the licensee. Nevertheless, the removal procedure and the measuring techniques to be applied for the different types of materials need an agreement from the competent authority. In Germany a maximum value of 10% of the clearance values has been established in different licenses as a criterion for the application of removal. As approximately 2/3 of the total mass of a nuclear power plant is not expected to be contaminated or activated there is a need for such a procedure of removal for this non contaminated material without any regulatory control especially in the case of decommissioning. A remarkable example is NPP Stade where in the last three years more than 8600 Mg were disposed of by removal and only 315 Mg were released by clearance, even before the decommissioning licensing procedure was finished. (authors)

Feinhals, J.; Kelch, A. [TUV NORD SysTec GmbH and Co. KG, Hamburg (Germany); Kunze, V. [Federal Office for Radiation Protection, Salzgitter (Germany)

2007-07-01T23:59:59.000Z

390

Health Consultation Assessment of Soil Exposures in Communities Adjacent to the Walter Coke, Inc. Site  

E-Print Network (OSTI)

A health consultation is a verbal or written response from ATSDR or ATSDR’s Cooperative Agreement Partners to a specific request for information about health risks related to a specific site, a chemical release, or the presence of hazardous material. In order to prevent or mitigate exposures, a consultation may lead to specific actions, such as restricting use of or replacing water supplies; intensifying environmental sampling; restricting site access; or removing the contaminated material. In addition, consultations may recommend additional public health actions, such as conducting health surveillance activities to evaluate exposure or trends in adverse health outcomes; conducting biological indicators of exposure studies to assess exposure; and providing health education for health care providers and community members. This concludes the health consultation process for this site, unless additional information is obtained by ATSDR or ATSDR’s Cooperative Agreement Partner which, in the Agency’s opinion, indicates a need to revise or append the conclusions previously issued. You May Contact ATSDR Toll Free at

Birmingham Al

2013-01-01T23:59:59.000Z

391

Carbons for battery anodes prepared using inorganic templates  

DOE Green Energy (OSTI)

Unique carbons with demonstrated utility as anodes for lithium secondary batteries have been prepared by heating hydrocarbons within an inorganic template. Disordered carbons with novel and desirable molecular porosity were synthesized by the pyrolysis of pyrene at 700 C within a pillared clay. The clay was removed by treatment with acid, leaving behind carbons with 15 to 50 {angstrom} holes. These holey carbons, when converted into electrodes, allow rapid diffusion of the lithium into and out of a carbon. Favorable results have been obtained in several tests, for example, a reversible capacity of 825 mAh/g has been achieved, about four times greater than commercial batteries using convention pyrolytic carbon.

Winans, R.E.; Carrado, K.A.; Sandi, G. [Argonne National Lab., IL (United States). Chemistry Div.

1997-07-01T23:59:59.000Z

392

Large Component Removal/Disposal  

Science Conference Proceedings (OSTI)

This paper describes the removal and disposal of the large components from Maine Yankee Atomic Power Plant. The large components discussed include the three steam generators, pressurizer, and reactor pressure vessel. Two separate Exemption Requests, which included radiological characterizations, shielding evaluations, structural evaluations and transportation plans, were prepared and issued to the DOT for approval to ship these components; the first was for the three steam generators and one pressurizer, the second was for the reactor pressure vessel. Both Exemption Requests were submitted to the DOT in November 1999. The DOT approved the Exemption Requests in May and July of 2000, respectively. The steam generators and pressurizer have been removed from Maine Yankee and shipped to the processing facility. They were removed from Maine Yankee's Containment Building, loaded onto specially designed skid assemblies, transported onto two separate barges, tied down to the barges, th en shipped 2750 miles to Memphis, Tennessee for processing. The Reactor Pressure Vessel Removal Project is currently under way and scheduled to be completed by Fall of 2002. The planning, preparation and removal of these large components has required extensive efforts in planning and implementation on the part of all parties involved.

Wheeler, D. M.

2002-02-27T23:59:59.000Z

393

Multipollutant Removal with WOWClean® System  

E-Print Network (OSTI)

WOW Energy built and tested its multipollutant removal WOWClean® system in a development program with the Texas Commission on Environmental Quality (TCEQ). A 2,500 ACFM mobile unit was built to field test the removal of air pollution constituents from the flue gas of a power plant and demonstrate the technology. The system integrates proven emission reduction techniques into a single, multi-pollutant reduction system and is designed to remove Mercury, SOx, NOx, particulates, heavy metals and other pollutants from low temperature flue gases. Its advantages include robust operation, lower investment, lower operating cost and high removal rates. The WOWClean® system has been tested on flue gases resulting from the combustion of diverse fuels such as petcoke, coal, wood, diesel and natural gas. In addition to significant removal of CO2, test results demonstrate the capability to reduce 99.5% SOx (from levels as high as 2200 ppm), 90% reduction of NOx, and > 90% heavy metals. The paper will include details of the multi-pollutant system along with test results.

Romero, M.

2010-01-01T23:59:59.000Z

394

Vietnam HEU Removal | National Nuclear Security Administration  

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

Removal NNSANews posted a photo: Vietnam HEU Removal A truck carrying the last highly enriched uranium in Vietnam winds through the Vietnamese countryside. Facebook Twitter Youtube...

395

NETL: News Release - DOE Asks Regional Partners to Validate Carbon...  

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

given to a family of methods for removing greenhouse gases, especially carbon dioxide (CO2), from power plant emissions or from the air itself, and securely storing the gases in...

396

NETL: Carbon Storage - Carbon Sequestration Leadership Forum  

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

CSLF Carbon Storage Carbon Sequestration Leadership Forum CSLF Logo The Carbon Sequestration Leadership Forum (CSLF) is a voluntary climate initiative of industrially developed and...

397

Method of immobilizing carbon dioxide from gas streams  

DOE Patents (OSTI)

This invention is a method for rapidly and continuously immobilizing carbon dioxide contained in various industrial off-gas streams, the carbon dioxide being immobilized as dry, stable, and substantially water-insoluble particulates. Briefly, the method comprises passing the gas stream through a fixed or fluidized bed of hydrated barium hydroxide to remove and immobilize the carbon dioxide by converting the bed to barium carbonate. The method has several important advantages: it can be conducted effectively at ambient temperature; it provides a very rapid reaction rate over a wide range of carbon dioxide concentrations; it provides high decontamination factors; and it has a high capacity for carbon dioxide. The invention is especially well suited for the removal of radioactive carbon dioxide from off-gases generated by nuclear-fuel reprocessing facilities and nuclear power plants.

Holladay, David W. (Knoxville, TN); Haag, Gary L. (Oliver Springs, TN)

1979-01-01T23:59:59.000Z

398

RESEARCH ON CARBON PRODUCTS FROM COAL USING AN EXTRACTIVE PROCESS  

SciTech Connect

This report presents the results of a one-year effort directed at the exploration of the use of coal as a feedstock for a variety of industrially-relevant carbon products. The work was basically divided into three focus areas. The first area dealt with the acquisition of laboratory equipment to aid in the analysis and characterization of both the raw coal and the coal-derived feedstocks. Improvements were also made on the coal-extraction pilot plant which will now allow larger quantities of feedstock to be produced. Mass and energy balances were also performed on the pilot plant in an attempt to evaluate the scale-up potential of the process. The second focus area dealt with exploring hydrogenation conditions specifically aimed at testing several less-expensive candidate hydrogen-donor solvents. Through a process of filtration and vacuum distillation, viable pitch products were produced and evaluated. Moreover, a recycle solvent was also isolated so that the overall solvent balance in the system could be maintained. The effect of variables such as gas pressure and gas atmosphere were evaluated. The pitch product was analyzed and showed low ash content, reasonable yield, good coking value and a coke with anisotropic optical texture. A unique plot of coke yield vs. pitch softening point was discovered to be independent of reaction conditions or hydrogen-donor solvent. The third area of research centered on the investigation of alternate extraction solvents and processing conditions for the solvent extraction step. A wide variety of solvents, co-solvents and enhancement additives were tested with varying degrees of success. For the extraction of raw coal, the efficacy of the alternate solvents when compared to the benchmark solvent, N-methyl pyrrolidone, was not good. However when the same coal was partially hydrogenated prior to solvent extraction, all solvents showed excellent results even for extractions performed at room temperature. Standard analyses of the extraction products indicated that they had the requisite properties of viable carbon-product precursors.

Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo; Chong Chen; Brian Bland; David Fenton

2002-03-31T23:59:59.000Z

399

Metal Cutting for Large Component Removal  

Science Conference Proceedings (OSTI)

Decommissioning of commercial nuclear power plants presents technological challenges. One major challenge is the removal of large components mainly consisting of the reactor vessel, steam generators and pressurizer. In order to remove and package these large components nozzles must be cut from the reactor vessel to precise tolerances. In some cases steam generators must be segmented for size and weight reduction. One innovative technology that has been used successfully at several commercial nuclear plant decommissioning is diamond wire sawing. Diamond wire sawing is performed by rotating a cable with diamond segments attached using a flywheel approximately 24 inches in diameter driven remotely by a hydraulic pump. Tension is provided using a gear rack drive which also takes up the slack in the wire. The wire is guided through the use of pulleys keeps the wire in a precise location. The diamond wire consists of 1/4 inch aircraft cable with diamond beads strung over the cable separated by springs and brass crimps. Standard wire contains 40 diamond beads per meter and can be made to any length. Cooling the wire and controlling the spread of contamination presents significant challenges. Under normal circumstances the wire is cooled and the cutting kerf cleaned by using water. In some cases of reactor nozzle cuts the use of water is prohibited because it cannot be controlled. This challenge was solved by using liquid Carbon Dioxide as the cooling agent. The liquid CO{sub 2} is passed through a special nozzle which atomizes the liquid into snowflakes which is introduced under pressure to the wire. The snowflakes attach to the wire keeping it cool and to the metal shavings. As the CO{sub 2} and metal shavings are released from the wire due to its fast rotation, the snowflakes evaporate leaving only the fine metal shavings as waste. Secondary waste produced is simply the small volume of fine metal shavings removed from the cut surface. Diamond wire sawing using CO{sub 2} cooling has been employed for cutting the reactor nozzles at San Onofre Unit 1 and at Connecticut Yankee. These carbon steel nozzles ranged up to 54 inch diameter with a 15 inch thick wall and an interior stainless cladding. Diamond wire sawing using traditional water cooling has been used to segment the reactor head at Rancho Seco and for cutting reactor nozzles and control rod drive tubes at Dairyland Power's Lacrosse BWR project. Advantages: - ALARA: All cutting is preformed remotely significantly reducing dose. Stringing of wires is accomplished using long handle tools. - Secondary waste is reduced to just the volume of material cut with the diamond wire. - The potential for airborne contamination is eliminated. Due to the flexibility of the wire, any access restrictions and interferences can be accommodated using pulleys and long handle tools. - The operation is quiet. Disadvantages: - With Liquid Carbon Dioxide cooling and cleaning, delivery of the material must be carefully planned. The longer the distance from the source to the cut area, the greater the chance for pressure drop and subsequent problems with line freezing. - Proper shrouding and ventilation are required for environmental reasons. In each case, the metal structures were cut at a precise location. Radiation dose was reduced significantly by operating the equipment from a remote location. The cuts were very smooth and completed on schedule. Each project must be analyzed individually and take into account many factors including access, radiological conditions, environmental conditions, schedule requirements, packaging requirements and size of cuts.

Hulick, Robert M. [Bluegrass Concrete Cutting Inc., 107 Mildred Street PO Box 427, Greenville, Alabama 36037 (United States)

2008-01-15T23:59:59.000Z

400

Evaluation of Innovative Fossil Fuel Power Plants with CO2 Removal  

Science Conference Proceedings (OSTI)

This interim report presents initial results of an ongoing study of the potential cost of electricity (COE) produced in both conventional and innovative fossil fueled power plants that incorporate carbon dioxide (CO2) removal for subsequent sequestration or use. The baseline cases are natural gas combined cycle (NGCC) and ultra-supercritical pulverized coal (PC) plants, with and without post combustion CO2 removal, and integrated gasification combined cycle (IGCC) plants, with and without pre-combustion ...

2000-12-07T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" from the National Library of EnergyBeta (NLEBeta).
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401

Forecast Technical Document Felling and Removals  

E-Print Network (OSTI)

Forecast Technical Document Felling and Removals Forecasts A document describing how volume fellings and removals are handled in the 2011 Production Forecast system. Tom Jenkins Robert Matthews Ewan Mackie Lesley Halsall #12;PF2011 ­ Felling and removals forecasts Background A fellings and removals

402

High removal rate laser-based coating removal system  

Science Conference Proceedings (OSTI)

A compact laser system is disclosed that removes surface coatings (such as paint, dirt, etc.) at a removal rate as high as 1,000 ft{sup 2}/hr or more without damaging the surface. A high repetition rate laser with multiple amplification passes propagating through at least one optical amplifier is used, along with a delivery system consisting of a telescoping and articulating tube which also contains an evacuation system for simultaneously sweeping up the debris produced in the process. The amplified beam can be converted to an output beam by passively switching the polarization of at least one amplified beam. The system also has a personal safety system which protects against accidental exposures.

Matthews, D.L.; Celliers, P.M.; Hackel, L.; Da Silva, L.B.; Dane, C.B.; Mrowka, S.

1999-11-16T23:59:59.000Z

403

Desalination with carbon aerogel electrodes  

SciTech Connect

An electrically regenerated electrosorption process known as carbon aerogel CDI was developed for continuously removing ionic impurities from aqueous streams. A salt solution flows in a channel formed by pairs of parallel carbon aerogel electrodes. Each electrode has a very high BET surface area and very low resistivity. After polarization, anions and cations are removed from electrolyte by the electric field and electrosorbed onto the carbon aerogel. The solution is thus separated into two streams, brine and water. Based on this, carbon aerogel CDI appears to be an energy-efficient alternative to evaporation, electrodialysis, and reverse osmosis. The energy required by this process is about QV/2, plus losses. Estimated energy requirement for sea water desalination is 18-27 Wh gal{sup -1}, depending on cell voltage and flow rate. The requirement for brackish water desalination is less, 1.2-2.5 Wh gal{sup -1} at 1600 ppM. This is assuming that stored electrical energy is reclaimed during regeneration.

Farmer, J.C.; Richardson, J.H.; Fix, D.V.

1996-10-21T23:59:59.000Z

404

DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS  

Science Conference Proceedings (OSTI)

The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. A process has been developed which results in high quality binder pitch suitable for use in graphite electrodes or carbon anodes. A detailed description of the protocol is given by Clendenin. Briefly, aromatic heavy oils are hydro-treated under mild conditions in order to increase their ability to dissolve coal. An example of an aromatic heavy oil is Koppers Carbon Black Base (CBB) oil. CBB oil has been found to be an effective solvent and acceptably low cost (i.e., significantly below the market price for binder pitch, or about $280 per ton at the time of this writing). It is also possible to use solvents derived from hydrotreated coal and avoid reliance on coke oven recovery products completely if so desired.

Elliot B. Kennel; Philip L. Biedler; Chong Chen; Dady Dadyburjor; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

2005-04-13T23:59:59.000Z

405

DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS  

DOE Green Energy (OSTI)

The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. The largest applications are those which support metals smelting, such as anodes for aluminum smelting and electrodes for arc furnaces. Other carbon products include materials used in creating fuels for the Direct Carbon Fuel Cell, metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, coking and composite fabrication continued using coal-derived samples. These samples were tested in direct carbon fuel cells. Methodology was refined for determining the aromatic character of hydro treated liquid, based on Nuclear Magnetic Resonance (NMR) and Fourier Transform Infrared (FTIR). Tests at GrafTech International showed that binder pitches produced using the WVU solvent extraction protocol can result in acceptable graphite electrodes for use in arc furnaces. These tests were made at the pilot scale.

Elliot B. Kennel; R. Michael Bergen; Stephen P. Carpenter; Dady Dadyburjor; Manoj Katakdaunde; Liviu Magean; Alfred H. Stiller; W. Morgan Summers; John W. Zondlo

2006-05-12T23:59:59.000Z

406

The Carbon Cycle  

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

Carbon Cycle Print E-mail U.S. Carbon Cycle Science Program U.S. Carbon Cycle Science Program The U.S. Carbon Cycle Science Program, in consultation with the Carbon Cycle...

407

Carbon Sequestration  

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

David a. Lang David a. Lang Project Manager National Energy Technology Laboratory 626 Cochrans Mill Road P.O. Box 10940 Pittsburgh, PA 15236 412-386-4881 david.lang@netl.doe.gov andrew chizmeshya Arizona State University Center for Solid State Science Tempe, AZ 85287-1704 480-965-6072 chizmesh@asu.edu A Novel ApproAch to MiNerAl cArboNAtioN: eNhANciNg cArboNAtioN While AvoidiNg MiNerAl pretreAtMeNt process cost Background Carbonation of the widely occurring minerals of the olivine group, such as forsterite (Mg 2 SiO 4 ), is a potential large-scale sequestration process that converts CO 2 into the environmentally benign mineral magnesite (MgCO 3 ). Because the process is exothermic, it inherently offers low-cost potential. Enhancing carbonation reactivity is the key to economic viability. Previous

408

Method for aqueous gold thiosulfate extraction using copper-cyanide pretreated carbon adsorption  

Science Conference Proceedings (OSTI)

A gold thiosulfate leaching process uses carbon to remove gold from the leach liquor. The activated carbon is pretreated with copper cyanide. A copper (on the carbon) to gold (in solution) ratio of at least 1.5 optimizes gold recovery from solution. To recover the gold from the carbon, conventional elution technology works but is dependent on the copper to gold ratio on the carbon.

Young, Courtney; Melashvili, Mariam; Gow, Nicholas V

2013-08-06T23:59:59.000Z

409

Chloride removal from plutonium alloy  

Science Conference Proceedings (OSTI)

SRP is evaluating a program to recover plutonium from a metallic alloy that will contain chloride salt impurities. Removal of chloride to sufficiently low levels to prevent damaging corrosion to canyon equipment is feasible as a head-end step following dissolution. Silver nitrate and mercurous nitrate were each successfully used in laboratory tests to remove chloride from simulated alloy dissolver solution containing plutonium. Levels less than 10 ppM chloride were achieved in the supernates over the precipitated and centrifuged insoluble salts. Also, less than 0.05% loss of plutonium in the +3, +4, or +6 oxidation states was incurred via precipitate carrying. These results provide impetus for further study and development of a plant-scale process to recover plutonium from metal alloy at SRP.

Holcomb, H.P.

1983-01-01T23:59:59.000Z

410

Removing Barriers to Interdisciplinary Research  

E-Print Network (OSTI)

A significant amount of high-impact contemporary scientific research occurs where biology, computer science, engineering and chemistry converge. Although programmes have been put in place to support such work, the complex dynamics of interdisciplinarity are still poorly understood. In this paper we interrogate the nature of interdisciplinary research and how we might measure its "success", identify potential barriers to its implementation, and suggest possible mechanisms for removing these impediments.

Naomi Jacobs; Martyn Amos

2010-12-19T23:59:59.000Z

411

NETL Patented CO2-Removal Sorbents Promise Power and Cost Savings |  

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

Patented CO2-Removal Sorbents Promise Power and Cost Savings Patented CO2-Removal Sorbents Promise Power and Cost Savings NETL Patented CO2-Removal Sorbents Promise Power and Cost Savings May 30, 2012 - 1:00pm Addthis Washington, DC - Carbon dioxide removal sorbents developed by the U.S. Department of Energy's (DOE) National Energy Technology Laboratory (NETL) could result in power and cost savings for users of some heating, ventilation and air conditioning (HVAC) systems under a recently signed license agreement. NETL, the research and development laboratory for DOE's Office of Fossil Energy, entered into a patent license agreement with Boston-based Enverid Systems Inc. for NETL-developed solid sorbents that remove CO2 from gas streams. NETL's sorbents will be incorporated into an Enverid product called EnClaire™, which adds on to HVAC systems to reduce power

412

Determination of the effects caused by different polymers on coal fluidity during carbonization using high-temperature {sup 1}H NMR and rheometry  

SciTech Connect

The effects of blending polyethylene (PE), polystyrene (PS), poly(ethyleneterephthalate) (PET), a flexible polyurethane (FPU), and a car shredded fluff waste (CSF) on fluidity development of a bituminous coal during carbonization have been studied by means of high-torque, small-amplitude controlled-strain rheometry and in situ high-temperature {sup 1}H NMR spectroscopy. The most detrimental effects were caused by PET and PS, which completely destroyed the fluidity of the coal. The CSF had a deleterious effect on coal fluidity similar to that of PET, although the deleterious effect on the viscoelastic properties of the coal were less pronounced than those of PET and PS. On the contrary, the addition of 10 wt % PE caused a slight reduction in the concentration of fluid hydrogen and an increase in the minimum complex viscosity, and the addition of 10 wt % FPU reduced the concentration of fluid hydrogen without changing the viscoelastic properties of the coal. Although these results suggest that these two plastics could potentially be used as additives in coking blends without compromising coke porosity, it was found that the semicoke strengths were reduced by adding 2 wt % FPU and 5 wt % PE. Therefore, it is unlikely that more than 2 wt % of a plastic waste could be added to a coal blend without deterioration in coke quality. 35 refs., 11 figs., 3 tabs.

Miguel Castro Diaz; Lucky Edecki; Karen M. Steel; John W. Patrick; Colin E. Snape [Nottingham University, Nottingham (United Kingdom). Nottingham Fuel and Energy Centre, School of Chemical, Environmental and Mining Engineering

2008-01-15T23:59:59.000Z

413

Numerical modeling of the aerodynamics, heat exchange, and combustion of a polydisperse ensemble of coke-ash particles in ascending axisymmetric two-phase flow  

Science Conference Proceedings (OSTI)

A two-dimensional stationary model of motion, heat and mass exchange, and chemical reaction of polydisperse coke and ash particles in ascending gas-suspension flow has been constructed with allowance for the turbulent and pseudo turbulent mechanisms of transfer in the dispersed phase. The system of equations that describes motion and heat transfer in the solid phase has been closed at the level of the equations for the second moments of velocity and temperature pulsations, whereas the momentum equations of the carrying medium have been closed using the equation for turbulent gas energy, which allows for the influence of the particles and heterogeneous reactions.

B.B. Rokhman [National Academy of Sciences of Ukraine, Kiev (Ukraine). Institute of Coal Power Technologies

2009-07-15T23:59:59.000Z

414

Reductive dissolution approaches to removal of uranium from contaminated soils  

SciTech Connect

Traditional approaches to uranium recovery from ores have employed oxidation of U(IV) minerals to form the uranyl cation which is subsequently complexed by carbonate or maintained in solution by strong acids. Reductive approaches for uranium decontamination have been limited to removing soluble uranium from solutions by formation of U{sup 4+} which readily hydrolyses and precipitates. As part of the Uranium in Soils Integrated Demonstration, we have developed a reductive approach to solubilization of uranium from contaminated soils which employs reduction to destabilize U(VI) solid and sorbed species, and strong chelators for U(IV) to prevent hydrolysis and solubilize the reduced from. This strategy has particular application to sites where the uranium is present primarily as intractable U(VI) phases and where high fractions of the contamination must be removed to meet regulatory requirements.

Brainard, J.R.; Iams, H.D.; Strietelmeier, B.A.; Del-Rio Garcia, M.

1994-06-01T23:59:59.000Z

415

The effects of moderate coal cleaning on the microbial removal of organic sulfur. [Rhodococcuc rhodochrous  

SciTech Connect

The purpose of this project is to investigate the possibilities of developing an integrated physical/chemical/microbial process for the precombustion removal of sulfur from coal. An effective pre- combustion coal desulfurization process should ideally be capable of removing both organic and inorganic sulfur. A variety of techniques exist for the removal of inorganic sulfur from coal, but there is currently no cost-effective method for the pre-combustion removal of organic sulfur. Recent developments have demonstrated that microorganisms are capable of specifically cleaving carbon-sulfur bonds and removing substantial amounts of organic sulfur from coal. However, lengthy treatment times are required. Moreover, the removal of organic sulfur form coal by microorganisms is hampered by the fact that, as a solid substrate, it is difficult to bring microorganisms in contact with the entirety of a coal sample. This study will examine the suitability of physically/chemically treated coal sample for subsequent biodesulfurization. Physical/chemical processes primarily designed for the removal of pyritic sulfur may also cause substantial increases in the porosity and surface area of the coal which may facilitate the subsequent removal of organic sulfur by microoganisms. During the current quarter, coal samples that have been chemically pretreated with methanol, ammonia, and isopropanol were examined for the removal of organic sulfur by the microbial culture IGTS8, an assay for the presence of protein in coal samples was developed, and a laboratory-scale device for the explosive comminution of coal was designed and constructed.

Srivastava, V.J.

1991-01-01T23:59:59.000Z

416

Thief Carbon Catalyst for Oxidation of Mercury in Effluent Stream  

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

Carbon Catalyst for Oxidation of Mercury in Effluent Carbon Catalyst for Oxidation of Mercury in Effluent Stream Contact NETL Technology Transfer Group techtransfer@netl.doe.gov January 2012 Significance * Oxidizes heavy metal contaminants, especially mercury, in gas streams * Uses partially combusted coal ("Thief" carbon) * Yields an inexpensive catalyst * Cheap enough to be a disposable catalyst * Cuts long-term costs * Simultaneously addresses oxidation and adsorption issues Applications * Any process requiring removal of heavy

417

NETL: Carbon Capture FAQs  

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

How is CO2 captured? How is CO2 captured? Chilled Ammonia CO2 Capture Process Facility at American Electric Power's (AEP) Mountaineer Plant Chilled Ammonia CO2 Capture Process Facility at American Electric Power's (AEP) Mountaineer Plant Carbon dioxide (CO2) capture involves separating CO2 from other gases generated by industrial processes or burning fossil fuels. CO2 capture can remove as much as 95% of the CO2 from these processes. There are two major types of anthropogenic CO2 sources: mobile and stationary. Mobile sources include things like cars, trucks, trains, boats, and aircrafts that burn fossil fuels and generate CO2. Capturing CO2 from mobile sources is currently impractical. Stationary sources include power plants and industrial facilities that burn fossil fuels, as

418

Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon...  

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

Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and Carbon-13 in Methane Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and...

419

Carbon Dioxide Capture from Integrated Gasification Combined Cycle Gas Streams Using the Ammonium Carbonate-Ammonium Bicarbonate Process  

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

Integrated Integrated Gasification Combined Cycle Gas Streams Using the Ammonium Carbonate- Ammonium Bicarbonate Process Description Current commercial processes to remove carbon dioxide (CO 2 ) from conventional power plants are expensive and energy intensive. The objective of this project is to reduce the cost associated with the capture of CO 2 from coal based gasification processes, which convert coal and other carbon based feedstocks to synthesis gas.

420

Fundamental investigation of slag/carbon interactions in electric arc furnace steelmaking process.  

E-Print Network (OSTI)

??This work investigates the interactions of carbonaceous materials (metallurgical coke, natural graphite and HDPE/coke blends) with three EAF slags [FeO: 24% to 32%]. Experiments were… (more)

Rahman, Muhammad Mahfuzur

2010-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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.


421

Carbon supercapacitors  

SciTech Connect

Carbon supercapacitors are represented as distributed RC networks with transmission line equivalent circuits. At low charge/discharge rates and low frequencies these networks approximate a simple series R{sub ESR}C circuit. The energy efficiency of the supercapacitor is limited by the voltage drop across the ESR. The pore structure of the carbon electrode defines the electrochemically active surface area which in turn establishes the volume specific capacitance of the carbon material. To date, the highest volume specific capacitance reported for a supercapacitor electrode is 220F/cm{sup 3} in aqueous H{sub 2}SO{sub 4} (10) and {approximately}60 F/cm{sup 3} in nonaqueous electrolyte (8).

Delnick, F.M.

1993-11-01T23:59:59.000Z

422

Carbon particles  

DOE Patents (OSTI)

A method and apparatus whereby small carbon particles are made by pyrolysis of a mixture of acetylene carried in argon. The mixture is injected through a nozzle into a heated tube. A small amount of air is added to the mixture. In order to prevent carbon build-up at the nozzle, the nozzle tip is externally cooled. The tube is also elongated sufficiently to assure efficient pyrolysis at the desired flow rates. A key feature of the method is that the acetylene and argon, for example, are premixed in a dilute ratio, and such mixture is injected while cool to minimize the agglomeration of the particles, which produces carbon particles with desired optical properties for use as a solar radiant heat absorber.

Hunt, Arlon J. (Oakland, CA)

1984-01-01T23:59:59.000Z

423

Natural gas: Removing the obstacles  

Science Conference Proceedings (OSTI)

Defining and then figuring out how to remove whatever obstacles may be blocking the wider use of natural gas was the purpose of a conference held early last month in Phoenix, Arizona. The unique, three-day event was jointly sponsored by the U.S. Department of Energy (DOE) and the National Association of Regulatory Utility Commissioners (NARUC). It drew an overflow crowd of more than 500, with a registration list that read like a Who's Who of the natural gas industry. This article summarizes some of the main points of this conference.

Romo, C.

1992-03-15T23:59:59.000Z

424

Solvent cleaning system and method for removing contaminants from solvent used in resin recycling  

DOE Patents (OSTI)

A two step solvent and carbon dioxide based system that produces essentially contaminant-free synthetic resin material and which further includes a solvent cleaning system for periodically removing the contaminants from the solvent so that the solvent can be reused and the contaminants can be collected and safely discarded in an environmentally safe manner.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee' s Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2009-01-06T23:59:59.000Z

425

Material Removal and Disposition | National Nuclear Security...  

National Nuclear Security Administration (NNSA)

Removal and Disposition | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response...

426

Carbon microtubes  

DOE Patents (OSTI)

A carbon microtube comprising a hollow, substantially tubular structure having a porous wall, wherein the microtube has a diameter of from about 10 .mu.m to about 150 .mu.m, and a density of less than 20 mg/cm.sup.3. Also described is a carbon microtube, having a diameter of at least 10 .mu.m and comprising a hollow, substantially tubular structure having a porous wall, wherein the porous wall comprises a plurality of voids, said voids substantially parallel to the length of the microtube, and defined by an inner surface, an outer surface, and a shared surface separating two adjacent voids.

Peng, Huisheng (Shanghai, CN); Zhu, Yuntian Theodore (Cary, NC); Peterson, Dean E. (Los Alamos, NM); Jia, Quanxi (Los Alamos, NM)

2011-06-14T23:59:59.000Z

427

High Efficiency Direct Carbon and Hydrogen Fuel Cells for Fossil Fuel Power Generation  

SciTech Connect

Hydrogen he1 cells have been under development for a number of years and are now nearing commercial applications. Direct carbon fuel cells, heretofore, have not reached practical stages of development because of problems in fuel reactivity and cell configuration. The carbon/air fuel cell reaction (C + O{sub 2} = CO{sub 2}) has the advantage of having a nearly zero entropy change. This allows a theoretical efficiency of 100 % at 700-800 C. The activities of the C fuel and CO{sub 2} product do not change during consumption of the fuel. Consequently, the EMF is invariant; this raises the possibility of 100% fuel utilization in a single pass. (In contrast, the high-temperature hydrogen fuel cell has a theoretical efficiency of and changes in fuel activity limit practical utilizations to 75-85%.) A direct carbon fuel cell is currently being developed that utilizes reactive carbon particulates wetted by a molten carbonate electrolyte. Pure COZ is evolved at the anode and oxygen from air is consumed at the cathode. Electrochemical data is reported here for the carbon/air cell utilizing carbons derived from he1 oil pyrolysis, purified coal, purified bio-char and petroleum coke. At 800 O C, a voltage efficiency of 80% was measured at power densities of 0.5-1 kW/m2. Carbon and hydrogen fuels may be produced simultaneously at lugh efficiency from: (1) natural gas, by thermal decomposition, (2) petroleum, by coking or pyrolysis of distillates, (3) coal, by sequential hydrogasification to methane and thermal pyrolysis of the methane, with recycle of the hydrogen, and (4) biomass, similarly by sequential hydrogenation and thermal pyrolysis. Fuel production data may be combined with direct C and H2 fuel cell operating data for power cycle estimates. Thermal to electric efficiencies indicate 80% HHV [85% LHV] for petroleum, 75.5% HHV [83.4% LHV] for natural gas and 68.3% HHV [70.8% LHV] for lignite coal. Possible benefits of integrated carbon and hydrogen fuel cell power generation cycles are: (1) increased efficiency by a factor of up to 2 over many conventional fossil fuel steam plants, (2) reduced power generation cost, especially for increasing fossil fuel cost, (3) reduced CO2 emission per kWh, and (4) direct sequestration or reuse (e.g., in enhanced oil or NG recovery) of the CO{sub 2} product.

Steinberg, M; Cooper, J F; Cherepy, N

2002-01-02T23:59:59.000Z

428

Direct Carbon Fuel Cells: Assessment of their Potential as Solid Carbon Fuel Based Power Generation Systems  

SciTech Connect

Small-scale experimental work at Lawrence Livermore National Laboratory (LLNL) has confirmed that a direct carbon fuel cell (DCFC) containing a molten carbonate electrolyte completely reacts solid elemental carbon with atmospheric oxygen contained in ambient air at a temperature of 650-800 C. The efficiency of conversion of the chemical energy in the fuel to DC electricity is 75-80% and is a result of zero entropy change for this reaction and the fixed chemical potentials of C and CO{sub 2}. This is about twice as efficient as other forms power production processes that utilize solid fuels such as petroleum coke or coal. These range from 30-40% for coal fired conventional subcritical or supercritical boilers to 38-42% for IGCC plants. A wide range of carbon-rich solids including activated carbons derived from natural gas, petroleum coke, raw coal, and deeply de-ashed coal have been evaluated with similar conversion results. The rate of electricity production has been shown to correlate with disorder in the carbon structure. This report provides a preliminary independent assessment of the economic potential of DCFC for competitive power generation. This assessment was conducted as part of a Director's Research Committee Review of DCFC held at Lawrence Livermore National Laboratory (LLNL) on April 9, 2004. The key question that this assessment addresses is whether this technology, which appears to be very promising from a scientific standpoint, has the potential to be successfully scaled up to a system that can compete with currently available power generation systems that serve existing electricity markets. These markets span a wide spectrum in terms of the amount of power to be delivered and the competitive cost in that market. For example, DCFC technology can be used for the personal power market where the current competition for delivery of kilowatts of electricity is storage batteries, for the distributed generation market where the competition for on-site power generation in the range of 0.5 to 50 MW is small engines fueled with natural gas or liquid fuels or in the bulk power markets supplied usually by remote central station power plants with capacities of 250-1250 MW that deliver electricity to customers via the transmission and distribution grid. New power generation technology must be able to offer a significant cost advantage over existing technologies serving the same market to attract the interest of investors that are needed to provide funding for the development, demonstration, and commercialization of the technology. That path is both lengthy and expensive. One of the key drivers for any new power generation technology is the relative amount of pollutant emissions of all types, particularly those that are currently regulated or may soon be regulated. The new focus on greenhouse gas emissions offers a window of opportunity to DCFC technology because of its much higher conversion efficiency and the production of a very concentrated stream of CO{sub 2} in the product gas. This should offer a major competitive advantage if CO{sub 2} emissions are constrained by regulation in the future. The cost of CO{sub 2} capture, liquefaction, and pressurization has the potential to be much less costly with DCFC technology compared to other currently available forms of fossil fuel power generation.

Wolk, R

2004-04-23T23:59:59.000Z

429

Direct Carbon Fuel Cells: Assessment of their Potential as Solid Carbon Fuel Based Power Generation Systems  

DOE Green Energy (OSTI)

Small-scale experimental work at Lawrence Livermore National Laboratory (LLNL) has confirmed that a direct carbon fuel cell (DCFC) containing a molten carbonate electrolyte completely reacts solid elemental carbon with atmospheric oxygen contained in ambient air at a temperature of 650-800 C. The efficiency of conversion of the chemical energy in the fuel to DC electricity is 75-80% and is a result of zero entropy change for this reaction and the fixed chemical potentials of C and CO{sub 2}. This is about twice as efficient as other forms power production processes that utilize solid fuels such as petroleum coke or coal. These range from 30-40% for coal fired conventional subcritical or supercritical boilers to 38-42% for IGCC plants. A wide range of carbon-rich solids including activated carbons derived from natural gas, petroleum coke, raw coal, and deeply de-ashed coal have been evaluated with similar conversion results. The rate of electricity production has been shown to correlate with disorder in the carbon structure. This report provides a preliminary independent assessment of the economic potential of DCFC for competitive power generation. This assessment was conducted as part of a Director's Research Committee Review of DCFC held at Lawrence Livermore National Laboratory (LLNL) on April 9, 2004. The key question that this assessment addresses is whether this technology, which appears to be very promising from a scientific standpoint, has the potential to be successfully scaled up to a system that can compete with currently available power generation systems that serve existing electricity markets. These markets span a wide spectrum in terms of the amount of power to be delivered and the competitive cost in that market. For example, DCFC technology can be used for the personal power market where the current competition for delivery of kilowatts of electricity is storage batteries, for the distributed generation market where the competition for on-site power generation in the range of 0.5 to 50 MW is small engines fueled with natural gas or liquid fuels or in the bulk power markets supplied usually by remote central station power plants with capacities of 250-1250 MW that deliver electricity to customers via the transmission and distribution grid. New power generation technology must be able to offer a significant cost advantage over existing technologies serving the same market to attract the interest of investors that are needed to provide funding for the development, demonstration, and commercialization of the technology. That path is both lengthy and expensive. One of the key drivers for any new power generation technology is the relative amount of pollutant emissions of all types, particularly those that are currently regulated or may soon be regulated. The new focus on greenhouse gas emissions offers a window of opportunity to DCFC technology because of its much higher conversion efficiency and the production of a very concentrated stream of CO{sub 2} in the product gas. This should offer a major competitive advantage if CO{sub 2} emissions are constrained by regulation in the future. The cost of CO{sub 2} capture, liquefaction, and pressurization has the potential to be much less costly with DCFC technology compared to other currently available forms of fossil fuel power generation.

Wolk, R

2004-04-23T23:59:59.000Z

430

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

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

Pre-Combustion Carbon Capture by Pre-Combustion Carbon Capture by a Nanoporous, Superhydrophobic Membrane Contactor Process Background An important component of the Department of Energy (DOE) Carbon Sequestration Program is the development of carbon capture technologies for power systems. Pre-combustion carbon dioxide (CO2) capture refers to the removal of the carbon content of a fuel before it is burned, thereby converting a fossil resource to a carbon- free energy carrier. Pre-combustion CO2 capture is considered to be less expensive

431

NETL: Utilization Projects - Managing High-Carbon Ash  

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

fuels includes US. coals of various rank, international coals, and alternate fuels from wood, agricultural residues, petroleum cokes, and organic model compounds. The surfactant...

432

Characterization of Dry Aggregates in Carbon Anodes by Image ...  

Science Conference Proceedings (OSTI)

Anodes are mainly composed of dry aggregates such as calcined petroleum coke and recycled materials with pitch as the binder. Granulometry of the dry ...

433

Water-Gas Shift Membrane Reactor Studies  

E-Print Network (OSTI)

Coal, Petroleum coke, Biomass, Waste, etc. Gasifier Particulate Removal Air Separator Oxygen Air Steam

434

Refines Efficiency Improvement  

Science Conference Proceedings (OSTI)

Refinery processes that convert heavy oils to lighter distillate fuels require heating for distillation, hydrogen addition or carbon rejection (coking). Efficiency is limited by the formation of insoluble carbon-rich coke deposits. Heat exchangers and other refinery units must be shut down for mechanical coke removal, resulting in a significant loss of output and revenue. When a residuum is heated above the temperature at which pyrolysis occurs (340 C, 650 F), there is typically an induction period before coke formation begins (Magaril and Aksenova 1968, Wiehe 1993). To avoid fouling, refiners often stop heating a residuum before coke formation begins, using arbitrary criteria. In many cases, this heating is stopped sooner than need be, resulting in less than maximum product yield. Western Research Institute (WRI) has developed innovative Coking Index concepts (patent pending) which can be used for process control by refiners to heat residua to the threshold, but not beyond the point at which coke formation begins when petroleum residua materials are heated at pyrolysis temperatures (Schabron et al. 2001). The development of this universal predictor solves a long standing problem in petroleum refining. These Coking Indexes have great potential value in improving the efficiency of distillation processes. The Coking Indexes were found to apply to residua in a universal manner, and the theoretical basis for the indexes has been established (Schabron et al. 2001a, 2001b, 2001c). For the first time, a few simple measurements indicates how close undesired coke formation is on the coke formation induction time line. The Coking Indexes can lead to new process controls that can improve refinery distillation efficiency by several percentage points. Petroleum residua consist of an ordered continuum of solvated polar materials usually referred to as asphaltenes dispersed in a lower polarity solvent phase held together by intermediate polarity materials usually referred to as resins. The Coking Indexes focus on the amount of these intermediate polarity species since coke formation begins when these are depleted. Currently the Coking Indexes are determined by either titration or solubility measurements which must be performed in a laboratory. In the current work, various spectral, microscopic, and thermal techniques possibly leading to on-line analysis were explored for measuring the Coking Indexes.

WRI

2002-05-15T23:59:59.000Z

435

Electrokinetic removal of uranium from contaminated, unsaturated soils  

SciTech Connect

Electrokinetic remediation of uranium-contaminated soil was studied in a series of laboratory-scale experiments in test cells with identical geometry using quartz sand at approximately 10 percent moisture content. Uranium, when present in the soil system as an anionic complex, could be migrated through unsaturated soil using electrokinetics. The distance that the uranium migrated in the test cell was dependent upon the initial molar ratio of citrate to uranium used. Over 50 percent of the uranium was recovered from the test cells using the citrate and carbonate complexing agents over of period of 15 days. Soil analyses showed that the uranium remaining in the test cells had been mobilized and ultimately would have been extracted. Uranium extraction exceeded 90 percent in an experiment that was operated for 37 days. Over 70 percent of the uranium was removed from a Hanford waste sample over a 55 day operating period. Citrate and carbonate ligand utilization ratios required for removing 50 percent of the uranium from the uranium-contaminated sand systems were approximately 230 moles ligand per mole uranium and 1320 moles ligand per mole uranium for the waste. Modifying the operating conditions to increasing the residence time of the complexants is expected to improved the utilization efficiency of the complexing agent.

Booher, W.F. [IT Corp., Albuquerque, NM (United States); Lindgren, E.R.; Brady, P.V. [Sandia National Laboratories, Albuquerque, NM (United States)

1997-01-01T23:59:59.000Z

436

THERMALLY SHIELDED MOISTURE REMOVAL DEVICE  

DOE Patents (OSTI)

An apparatus is presented for removing moisture from the air within tanks by condensation upon a cartridge containing liquid air. An insulating shell made in two halves covers the cartridge within the evacuated system. The shell halves are hinged together and are operated by a system of levers from outside the tank with the motion translated through a sylphon bellows to cover and uncover the cartridge. When the condensation of moisture is in process, the insulative shell is moved away from the liquid air cartridge, and during that part of the process when there is no freezing out of moisture, the shell halves are closed on the cell so thnt the accumulated frost is not evaporated. This insulating shell greatly reduces the consumption of liquid air in this condensation process.

Miller, O.E.

1958-08-26T23:59:59.000Z

437

SILISIUM PRODUKSJONSPROSESS. ENERGI OG EKSERGI ANALYSE FOR  

E-Print Network (OSTI)

during silicon process [21] 69 A.3. The carbon in the coal removes the two oxygen atoms from the quartz. The main input to the process is one or more quartz types. Coal, coke woodchips and charcoal are carbon from mines in Egypt, Spain and Norway [11]. The quartz /quartzite is chosen based on the following

Kjelstrup, Signe

438

Coking - Energy Information Administration  

U.S. Energy Information Administration (EIA)

-No Data Reported; --= Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Notes: Idle refineries ...

439

Melter Glass Removal and Dismantlement  

Science Conference Proceedings (OSTI)

The U.S. Department of Energy (DOE) has been using vitrification processes to convert high-level radioactive waste forms into a stable glass for disposal in waste repositories. Vitrification facilities at the Savannah River Site (SRS) and at the West Valley Demonstration Project (WVDP) are converting liquid high-level waste (HLW) by combining it with a glass-forming media to form a borosilicate glass, which will ensure safe long-term storage. Large, slurry fed melters, which are used for this process, were anticipated to have a finite life (on the order of two to three years) at which time they would have to be replaced using remote methods because of the high radiation fields. In actuality the melters useable life spans have, to date, exceeded original life-span estimates. Initial plans called for the removal of failed melters by placing the melter assembly into a container and storing the assembly in a concrete vault on the vitrification plant site pending size-reduction, segregation, containerization, and shipment to appropriate storage facilities. Separate facilities for the processing of the failed melters currently do not exist. Options for handling these melters include (1) locating a facility to conduct the size-reduction, characterization, and containerization as originally planned; (2) long-term storing or disposing of the complete melter assembly; and (3) attempting to refurbish the melter and to reuse the melter assembly. The focus of this report is to look at methods and issues pertinent to size-reduction and/or melter refurbishment in particular, removing the glass as a part of a refurbishment or to reduce contamination levels (thus allowing for disposal of a greater proportion of the melter as low level waste).

Richardson, BS

2000-10-31T23:59:59.000Z

440

Nitrogen removal from natural gas  

SciTech Connect

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

1997-04-01T23:59:59.000Z

Note: This page contains sample records for the topic "remove carbon coke" 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.


441

Carbon | Open Energy Information  

Open Energy Info (EERE)

Carbon Sector Retrieved from "http:en.openei.orgwindex.php?titleCarbon&oldid271960" Categories: Articles with outstanding TODO tasks...

442

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

443

Carbon Additionality: Discussion Paper  

E-Print Network (OSTI)

Carbon Additionality: A review Discussion Paper Gregory Valatin November 2009 Forest Research. Voluntary Carbon Standards American Carbon Registry Forest Carbon Project Standard (ACRFCPS) 27 CarbonFix Standard (CFS) 28 Climate, Community and Biodiversity Standard (CCBS) 28 Forest Carbon Standard (FCS) 28

444

Process for removal of sulfur compounds from fuel gases  

DOE Patents (OSTI)

Fuel gases such as those produced in the gasification of coal are stripped of sulfur compounds and particulate matter by contact with molten metal salt. The fuel gas and salt are intimately mixed by passage through a venturi or other constriction in which the fuel gas entrains the molten salt as dispersed droplets to a gas-liquid separator. The separated molten salt is divided into a major and a minor flow portion with the minor flow portion passing on to a regenerator in which it is contacted with steam and carbon dioxide as strip gas to remove sulfur compounds. The strip gas is further processed to recover sulfur. The depleted, minor flow portion of salt is passed again into contact with the fuel gas for further sulfur removal from the gas. The sulfur depleted, fuel gas then flows through a solid absorbent for removal of salt droplets. The minor flow portion of the molten salt is then recombined with the major flow portion for feed to the venturi.

Moore, Raymond H. (Richland, WA); Stegen, Gary E. (Richland, WA)

1978-01-01T23:59:59.000Z

445

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

Science Conference Proceedings (OSTI)

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

Rizzo, Jeffrey

2010-04-30T23:59:59.000Z

446

Carbon Sequestration  

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

andrea Mcnemar andrea Mcnemar National Energy Technology Laboratory 3610 Collins Ferry Road P.O. Box 880 Morgantown, WV 26507-0880 304-285-2024 andrea.mcnemar@netl.doe.gov Gregory J. Elbring Principal Investigator Sandia National Laboratory P.O. Box 5800 Albuquerque, NM 87185 505-844-4904 gjelbri@sandia.gov GeoloGic SequeStration of carbon DioxiDe in a DepleteD oil reServoir: a comprehenSive moDelinG anD Site monitorinG project Background The use of carbon dioxide (CO 2 ) to enhance oil recovery (EOR) is a familiar and frequently used technique in the United States. The oil and gas industry has significant experience with well drilling and injecting CO 2 into oil-bearing formations to enhance production. While using similar techniques as in oil production, this sequestration field

447

Simultaneous removal of nitrogen oxides and sulfur oxides from combustion gases  

DOE Patents (OSTI)

A process for the simultaneous removal of sulfur oxides and nitrogen oxides from power plant stack gases comprising contacting the stack gases with a supported iron oxide catalyst/absorbent in the presence of sufficient reducing agent selected from the group consisting of carbon monoxide, hydrogen, and mixtures thereof, to provide a net reducing atmosphere in the SO.sub.x /NO.sub.x removal zone. The sulfur oxides are removed by absorption substantially as iron sulfide, and nitrogen oxides are removed by catalytic reduction to nitrogen and ammonia. The spent iron oxide catalyst/absorbent is regenerated by oxidation and is recycled to the contacting zone. Sulfur dioxide is also produced during regeneration and can be utilized in the production of sulfuric acid and/or sulfur.

Clay, David T. (Longview, WA); Lynn, Scott (Walnut Creek, CA)

1976-10-19T23:59:59.000Z

448

Catalytic steam gasification of carbon  

DOE Green Energy (OSTI)

Unsupported carbide powders with high specific surface area, namely {alpha}-WC (35 m{sup 2}/g, hexagonal), {beta}-WC{sub 0.61} (100 m{sup 2}/g, cubic face centered) and {beta}-WC{sub 0.5} (15 m{sup 2}/g, hexagonal) have been prepared. The key element in this preparation is the successful removal of surface polymeric carbon by careful gasification to methane by means of dihydrogen. These tungsten carbide powders have been used in catalytic reactions of oxidation of H{sub 2} and hydrogenolysis of alkanes, such as butane, hexane, and neopentane.

Boudart, M.

1990-12-31T23:59:59.000Z

449

Department of Energy Announces $41 Million Investment for Carbon Capture  

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

1 Million Investment for Carbon 1 Million Investment for Carbon Capture Development Department of Energy Announces $41 Million Investment for Carbon Capture Development August 25, 2011 - 1:36pm Addthis Washington, D.C. - The U.S. Department of Energy announced today the selection of 16 projects aimed at developing advanced post-combustion technologies for capturing carbon dioxide (CO2) from coal-fired power plants. The projects, valued at $41 million over three years, are focused on reducing the energy and cost penalties associated with applying currently available carbon capture technologies to existing and new power plants. The selections announced today will focus on developing carbon capture technologies that can achieve at least 90 percent CO2 removal and reduce the added costs at power plants with carbon capture systems to no more than

450

Department of Energy Announces $41 Million Investment for Carbon Capture  

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

$41 Million Investment for Carbon $41 Million Investment for Carbon Capture Development Department of Energy Announces $41 Million Investment for Carbon Capture Development August 25, 2011 - 1:00pm Addthis Washington, DC - The U.S. Department of Energy announced today the selection of 16 projects aimed at developing advanced post-combustion technologies for capturing carbon dioxide (CO2) from coal-fired power plants. The projects, valued at $41 million over three years, are focused on reducing the energy and cost penalties associated with applying currently available carbon capture technologies to existing and new power plants. The selections announced today will focus on developing carbon capture technologies that can achieve at least 90 percent CO2 removal and reduce the added costs at power plants with carbon capture systems to no more than

451

Energy Storage: Breakthrough in Battery Technologies (Carbon Cycle 2.0)  

DOE Green Energy (OSTI)

Nitash Balsara speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/

Balsara, Nitash

2010-02-04T23:59:59.000Z

452

Low Cost Solar Energy Conversion (Carbon Cycle 2.0)  

DOE Green Energy (OSTI)

Ramamoorthy Ramesh from LBNL's Materials Science Division speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 2, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/

Ramesh, Ramamoorthy

2010-02-04T23:59:59.000Z

453

Automatic CO/sub 2/ removal system and operation thereof  

SciTech Connect

A system is described for removing CO/sub 2/ from the manufactured process gas in an SNG manufacturing plant, the system operating the hot carbonate process wherein hot potassium carbonate solution absorbs CO/sub 2/ from the process gas under pressure in an absorber column and is regenerated by pressure reduction and steam stripping in a regenerator column and a reboiler before being returned to the absorber by a circulating pump. The system is completely automated and is controlled by a computer so that start-up, running and shut-down of the system is carried out automatically upon initiation by an operator, whereby the system is particularly suited for use in peak load SNG plants. For this purpose the system includes a solution make up tank, a solution storage tank, and a flushing water collection tank, preferably has all of its surfaces contacted by potassium carbonate solution made of stainless steel, and has sensors (F, L, T, P, AN, SG, and PH) and valve switches for transmitting information to the computer relating to the state of the system. The computer is programmed to operate the sequences of operation necessary to achieve the start-up, running and shut down of the system, operate loop controls on the solution levels in the absorber and regenerator columns, and on the rates of flow of solution to the absorber and of steam to the reboiler, and also to monitor the system parameters and to display data and signal alarm conditions.

Adams, K. J. G.; Bolt, N. T.; Siddique, Q. M.; Williams, T. P.

1985-01-01T23:59:59.000Z

454

Part 3: Removal Action | Department of Energy  

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

3: Removal Action 3: Removal Action Part 3: Removal Action Question: When may removal actions be initiated? Answer: Removal actions may be initiated when DOE determines that the action will prevent, minimize, stabilize, or eliminate a risk to health or the environment. The NCP specifies that the determination that a risk to health or the environment is appropriate for removal action should be based on: actual or potential exposure of humans, animals, or the food chain the presence of contained hazardous substances that pose a threat of release the threat of migration of the hazardous substances the threat of fire or explosion the availability of an appropriate Federal or State response capability [section 300.415(b)(2)]. In essence, where DOE identifies a threat of exposure to or migration of

455

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly ({gamma}-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly ({gamma}-glutamylcysteinyl)glycines having a particular number of monomer repeat units for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heavy metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, P.J.; Delhaize, E.; Robinson, N.J.; Unkefer, C.J.; Furlong, C.

1988-08-26T23:59:59.000Z

456

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly (.gamma.-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly (.gamma.-glutamylcysteinyl)glycines having a particular number of monomer repeat units for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heavy metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, Paul J. (Los Alamos, NM); Delhaize, Emmanuel (Los Alamos, NM); Robinson, Nigel J. (Durham, GB2); Unkefer, Clifford J. (Los Alamos, NM); Furlong, Clement (Seattle, WA)

1990-01-01T23:59:59.000Z

457

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly (.gamma.-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly (.gamma.-glutamylcysteinyl)glycines having a particular number of monomer repeat unit for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heayv metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, Paul J. (both Los Alamos, NM); Delhaize, Emmanuel (both Los Alamos, NM); Robinson, Nigel J. (Durham, GB2); Unkefer, Clifford J. (Los Alamos, NM); Furlong, Clement (Seattle, WA)

1990-11-13T23:59:59.000Z

458

Process for particulate removal from coal liquids  

DOE Patents (OSTI)

Suspended solid particulates are removed from liquefied coal products by first subjecting such products to hydroclone action for removal in the underflow of the larger size particulates, and then subjecting the overflow from said hydroclone action, comprising the residual finer particulates, to an electrostatic field in an electrofilter wherein such finer particulates are deposited in the bed of beads of dielectric material on said filter. The beads are periodically cleaned by backwashing to remove the accumulated solids.

Rappe, Gerald C. (Macungie, PA)

1983-01-01T23:59:59.000Z

459

Method for removing contaminants from plastic resin  

Science Conference Proceedings (OSTI)

A resin recycling method that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The method includes receiving the resin in container form. The containers are then ground into resin particles. The particles are exposed to a solvent, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. After separating the particles and the resin, a solvent removing agent is used to remove any residual solvent remaining on the resin particles after separation.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-12-09T23:59:59.000Z

460

Passive Core Decay Heat Removal Performance Guideline  

Science Conference Proceedings (OSTI)

Passive decay heat removal systems operate without pumps when normal heat removal systems are not available. Safety is ensured by confirming that an adequate thermal margin is provided to accommodate various operating conditions, design uncertainties, and degradation. Guidelines to ensure adequate thermal performance are provided for three different system configurations.This report introduces utility systems engineers to the design and operation of passive decay heat removal systems and ...

2013-11-26T23:59:59.000Z

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461

TESTING GUIDELINES FOR TECHNETIUM-99 ABSORPTION ON ACTIVATED CARBON  

SciTech Connect

CH2M HILL Plateau Remediation Company (CHPRC) is currently evaluating the potential use of activated carbon adsorption for removing technetium-99 from groundwater as a treatment method for the Hanford Site's 200 West Area groundwater pump-and-treat system. The current pump-and-treat system design will include an ion-exchange (IX) system for selective removal of technetium-99 from selected wells prior to subsequent treatment of the water in the central treatment system. The IX resin selected for technetium-99 removal is Purolite A530E. The resin service life is estimated to be approximately 66.85 days at the design technetium-99 loading rate, and the spent resin must be replaced because it cannot be regenerated. The resulting operating costs associated with resin replacement every 66.85 days are estimated at $0.98 million/year. Activated carbon pre-treatment is being evaluated as a potential cost-saving measure to offset the high operating costs associated with frequent IX resin replacement. This document is preceded by the Literature Survey of Technetium-99 Groundwater Pre-Treatment Option Using Granular Activated Carbon (SGW-43928), which identified and evaluated prior research related to technetium-99 adsorption on activated carbon. The survey also evaluated potential operating considerations for this treatment approach for the 200 West Area. The preliminary conclusions of the literature survey are as follows: (1) Activated carbon can be used to selectively remove technetium-99 from contaminated groundwater. (2) Technetium-99 adsorption onto activated carbon is expected to vary significantly based on carbon types and operating conditions. For the treatment approach to be viable at the Hanford Site, activated carbon must be capable of achieving a designated minimum technetium-99 uptake. (3) Certain radionuclides known to be present in 200 West Area groundwater are also likely to adsorb onto activated carbon. (4) Organic solvent contaminants of concern (COCs) will load heavily onto activated carbon and should be removed from groundwater upstream of the activated carbon pre-treatment system. Unless removed upstream, the adsorbed loadings of these organic constituents could exceed the land disposal criteria for carbon.

BYRNES ME

2010-09-08T23:59:59.000Z

462

Low pressure storage of natural gas on activated carbon  

DOE Green Energy (OSTI)

The introduction of natural gas to the transportation energy sector offers the possibility of displacing imported oil with an indigenous fuel. The barrier to the acceptance of natural gas vehicles (NGV) is the limited driving range due to the technical difficulties of on-board storage of a gaseous fuel. In spite of this barrier, compressed natural gas (CNG) vehicles are today being successfully introduced into the market place. The purpose of this work is to demonstrate an adsorbent natural gas (ANG) storage system as a viable alternative to CNG storage. It can be argued that low pressure ANG has reached near parity with CNG, since the storage capacity of CNG (2400 psi) is rated at 190 V/V, while low pressure ANG (500 psi) has reached storage capacities of 180 V/V in the laboratory. A program, which extends laboratory results to a full-scale vehicle test, is necessary before ANG technology will receive widespread acceptance. The objective of this program is to field test a 150 V/V ANG vehicle in FY 1994. As a start towards this goal, carbon adsorbents have been screened by Brookhaven for their potential use in a natural gas storage system. This paper reports on one such carbon, trade name Maxsorb, manufactured by Kansai Coke under an Amoco license.

Wegrzyn, J.; Wiesmann, H.; Lee, T.

1992-12-31T23:59:59.000Z

463

Low pressure storage of natural gas on activated carbon  

DOE Green Energy (OSTI)

The introduction of natural gas to the transportation energy sector offers the possibility of displacing imported oil with an indigenous fuel. The barrier to the acceptance of natural gas vehicles (NGV) is the limited driving range due to the technical difficulties of on-board storage of a gaseous fuel. In spite of this barrier, compressed natural gas (CNG) vehicles are today being successfully introduced into the market place. The purpose of this work is to demonstrate an adsorbent natural gas (ANG) storage system as a viable alternative to CNG storage. It can be argued that low pressure ANG has reached near parity with CNG, since the storage capacity of CNG (2400 psi) is rated at 190 V/V, while low pressure ANG (500 psi) has reached storage capacities of 180 V/V in the laboratory. A program, which extends laboratory results to a full-scale vehicle test, is necessary before ANG technology will receive widespread acceptance. The objective of this program is to field test a 150 V/V ANG vehicle in FY 1994. As a start towards this goal, carbon adsorbents have been screened by Brookhaven for their potential use in a natural gas storage system. This paper reports on one such carbon, trade name Maxsorb, manufactured by Kansai Coke under an Amoco license.

Wegrzyn, J.; Wiesmann, H.; Lee, T.

1992-01-01T23:59:59.000Z

464

Vietnam HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

NNSANews posted a photo: Vietnam HEU Removal A convoy escorting the last highly enriched uranium in Vietnam departs Dalat. Facebook Twitter Youtube Flickr Headlines Jul 23,...

465

System for removing contaminants from plastic resin  

DOE Patents (OSTI)

A resin recycling system that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The system includes receiving the resin in container form. A grinder grinds the containers into resin particles. The particles are exposed to a solvent in one or more solvent wash vessels, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. A separator is used to separate the resin particles and the solvent. The resin particles are then placed in solvent removing element where they are exposed to a solvent removing agent which removes any residual solvent remaining on the resin particles after separation.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee' s Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2010-11-23T23:59:59.000Z

466

Improved sulfur removal processes evaluated for IGCC  

SciTech Connect

An inherent advantage of Integrated Coal Gasification Combined Cycle (IGCC) electric power generation is the ability to easily remove and recover sulfur. During the last several years, a number of new, improved sulfur removal and recovery processes have been commercialized. An assessment is given of alternative sulfur removal processes for IGCC based on the Texaco coal gasifier. The Selexol acid gas removal system, Claus sulfur recovery, and SCOT tail gas treating are currently used in Texaco-based IGCC. Other processes considered are: Purisol, Sulfinol-M, Selefning, 50% MDEA, Sulften, and LO-CAT. 2 tables.

1986-12-01T23:59:59.000Z

467

Method for Removing Precipitates in Biofuel  

ORNL 2010-G00619/jcn UT-B ID 200902314 Method for Removing Precipitates in Biofuel Technology Summary At ORNL the application of ultrasonic energy, or ...

468

Internal Controls Over Classified Computersand Classified Removable...  

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

Classified Removable Media at theLawrence Livermore National Laboratory, IG-0628 Computers are used extensively in the full range of operations at Lawrence Livermore National...

469

Removal of radioisotopes from waste solutions  

DOE Patents (OSTI)

The invention comprises removing radioisotopes from waste liquids or solutions by passing these through filters and through a column containing a suitable salt of phosphoric acid. (Official Gazette)

Kirby, H.W.

1973-10-01T23:59:59.000Z

470

Tritium Removal Facility High Tritium Distillation Simulation.  

E-Print Network (OSTI)

??A dynamic model was developed for the distillation mechanism of the Darlington Tritium Removal Facility. The model was created using the commercial software package MATLAB/Simulink.… (more)

Zahedi, Polad

2013-01-01T23:59:59.000Z

471

Nanostructuring of Microporous Carbons with Carbon Nanotubes for ...  

Science Conference Proceedings (OSTI)

Presentation Title, Nanostructuring of Microporous Carbons with Carbon Nanotubes for Efficient Carbon Dioxide Capture. Author(s), Stephen C. Hawkins,  ...

472