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Note: This page contains sample records for the topic "hydrogen coal derived" from the National Library of EnergyBeta (NLEBeta).
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We encourage you to perform a real-time search of NLEBeta
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1

HYDROGEN PRODUCTION FOR FUEL CELLS VIA REFORMING COAL-DERIVED METHANOL  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feedstocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the sixth report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of January 1-March 31, 2005. This quarter saw progress in four areas. These areas are: (1) Autothermal reforming of coal derived methanol, (2) Catalyst deactivation, (3) Steam reformer transient response, and (4) Catalyst degradation with bluff bodies. All of the projects are proceeding on or slightly ahead of schedule.

Paul A. Erickson

2005-04-01T23:59:59.000Z

2

HYDROGEN PRODUCTION FOR FUEL CELLS VIA REFORMING COAL-DERIVED METHANOL  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feedstocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the ninth report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of October 1, 2005-December 31, 2005. This quarter saw progress in four areas. These areas are: (1) reformate purification, (2) heat transfer enhancement, (3) autothermal reforming coal-derived methanol degradation test; and (4) model development for fuel cell system integration. The project is on schedule and is now shifting towards the design of an integrated PEM fuel cell system capable of using the coal-derived product. This system includes a membrane clean up unit and a commercially available PEM fuel cell.

Paul A. Erickson

2006-01-01T23:59:59.000Z

3

HYDROGEN PRODUCTION FOR FUEL CELLS VIA REFORMING COAL-DERIVED METHANOL  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feed stocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the second report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of January 1--March 31, 2004. This quarter saw progress in five areas. These areas are: (1) Internal and external evaluations of coal based methanol and the fuel cell grade baseline fuel; (2) Experimental investigations of heat and mass transfer enhancement methods by flow field manipulation; (3) Design and set up of the autothermal reactor; (4) Steam reformation of Coal Based Methanol; and (5) Initial catalyst degradation studies. All of the projects are proceeding on or slightly ahead of schedule.

Paul A. Erickson

2004-04-01T23:59:59.000Z

4

HYDROGEN PRODUCTION FOR FUEL CELLS VIA REFORMING COAL-DERIVED METHANOL  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feedstocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the tenth report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of January 1-March 31, 2006. This quarter saw progress in six areas. These areas are: (1) The effect of catalyst dimension on steam reforming, (2) Transient characteristics of autothermal reforming, (3) Rich and lean autothermal reformation startup, (4) Autothermal reformation degradation with coal derived methanol, (5) Reformate purification system, and (6) Fuel cell system integration. All of the projects are proceeding on or slightly ahead of schedule.

Paul A. Erickson

2006-04-01T23:59:59.000Z

5

Hydrogen Production for Fuel Cells Via Reforming Coal-Derived Methanol  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feedstocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the seventh report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of April 1-June 31, 2005. This quarter saw progress in these areas. These areas are: (1) Steam reformer transient response, (2) Heat transfer enhancement, (3) Catalyst degradation, (4) Catalyst degradation with bluff bodies, and (5) Autothermal reforming of coal-derived methanol. All of the projects are proceeding on or slightly ahead of schedule.

Paul A. Erickson

2005-06-30T23:59:59.000Z

6

Hydrogen Production for Fuel Cells Via Reforming Coal-Derived Methanol  

SciTech Connect

Hydrogen can be produced from many feed stocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the fourth report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of July 1-Sept 30, 2004 along with a recap of progress from the start of the project on Oct 1, 2003 to Sept 30, 2004. All of the projects are proceeding on or slightly ahead of schedule. This year saw progress in several areas. These areas are: (1) External and internal evaluation of coal based methanol and a fuel cell grade baseline fuel, (2) Design set up and initial testing of three laboratory scale steam reformers, (3) Design, set up and initial testing of a laboratory scale autothermal reactor, (4) Hydrogen generation from coal-derived methanol using steam reformation, (5) Experiments to determine the axial and radial thermal profiles of the steam reformers, (6) Initial catalyst degradation studies with steam reformation and coal based methanol, and (7) Experimental investigations of heat and mass transfer enhancement methods by flow field manipulation. All of the projects are proceeding on or slightly ahead of schedule.

Paul A. Erickson

2004-09-30T23:59:59.000Z

7

Hydrogen Production for Fuel Cells Via Reforming Coal-Derived Methanol  

SciTech Connect

Hydrogen can be produced from many feed stocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the third report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of April 1-June 30, 2004. This quarter saw progress in five areas. These areas are: (1) External evaluation of coal based methanol and the fuel cell grade baseline fuel, (2) Design, set up and initial testing of the autothermal reactor, (3) Experiments to determine the axial and radial thermal profiles of the steam reformers, (4) Catalyst degradation studies, and (5) Experimental investigations of heat and mass transfer enhancement methods by flow field manipulation. All of the projects are proceeding on or slightly ahead of schedule.

Paul A. Erickson

2004-06-30T23:59:59.000Z

8

Hydrogen Production for Fuel Cells Via Reforming Coal-Derived Methanol  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feedstocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the eighth report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of October 1, 2004-September 30, 2005 and includes an entire review of the progress for year 2 of the project. This year saw progress in eight areas. These areas are: (1) steam reformer transient response, (2) steam reformer catalyst degradation, (3) steam reformer degradation tests using bluff bodies, (4) optimization of bluff bodies for steam reformation, (5) heat transfer enhancement, (6) autothermal reforming of coal derived methanol, (7) autothermal catalyst degradation, and (8) autothermal reformation with bluff bodies. The project is on schedule and is now shifting towards the design of an integrated PEM fuel cell system capable of using the coal-derived product. This system includes a membrane clean up unit and a commercially available PEM fuel cell.

Paul A. Erickson

2005-09-30T23:59:59.000Z

9

HYDROGEN PRODUCTION FOR FUEL CELLS VIA REFORMING COAL-DERIVED METHANOL  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feed stocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the first such report that will be submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of October 1--December 31, 2003. This quarter saw progress in three areas. These areas are: (1) Evaluations of coal based methanol and the fuel cell grade baseline fuel, (2) Design and set up of the autothermal reactor, as well as (3) Set up and data collection of baseline performance using the steam reformer. All of the projects are proceeding on schedule. During this quarter one conference paper was written that will be presented at the ASME Power 2004 conference in March 2004, which outlines the research direction and basis for looking at the coal to hydrogen pathway.

Paul A. Erickson

2004-04-01T23:59:59.000Z

10

Hydrogen from Coal  

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

Coal Coal Edward Schmetz Office of Sequestration, Hydrogen and Clean Coal Fuels U.S. Department of Energy DOE Workshop on Hydrogen Separations and Purification Technologies September 8, 2004 Presentation Outline ƒ Hydrogen Initiatives ƒ Hydrogen from Coal Central Production Goal ƒ Why Coal ƒ Why Hydrogen Separation Membranes ƒ Coal-based Synthesis Gas Characteristics ƒ Technical Barriers ƒ Targets ƒ Future Plans 2 3 Hydrogen from Coal Program Hydrogen from Coal Program FutureGen FutureGen Hydrogen Fuel Initiative Hydrogen Fuel Initiative Gasification Fuel Cells Turbines Gasification Fuel Cells Turbines Carbon Capture & Sequestration Carbon Capture & Sequestration The Hydrogen from Coal Program Supports the Hydrogen Fuel Initiative and FutureGen * The Hydrogen Fuel Initiative is a $1.2 billion RD&D program to develop hydrogen

11

Mechanochemical hydrogenation of coal  

DOE Patents (OSTI)

Hydrogenation of coal is improved through the use of a mechanical force to reduce the size of the particulate coal simultaneously with the introduction of gaseous hydrogen, or other hydrogen donor composition. Such hydrogen in the presence of elemental tin during this one-step size reduction-hydrogenation further improves the yield of the liquid hydrocarbon product.

Yang, Ralph T. (Tonawanda, NY); Smol, Robert (East Patchogue, NY); Farber, Gerald (Elmont, NY); Naphtali, Leonard M. (Washington, DC)

1981-01-01T23:59:59.000Z

12

Selective Catalytic Oxidation of Hydrogen Sulfide to Elemental Sulfur from Coal-Derived Fuel Gases  

SciTech Connect

The development of low cost, highly efficient, desulfurization technology with integrated sulfur recovery remains a principle barrier issue for Vision 21 integrated gasification combined cycle (IGCC) power generation plants. In this plan, the U. S. Department of Energy will construct ultra-clean, modular, co-production IGCC power plants each with chemical products tailored to meet the demands of specific regional markets. The catalysts employed in these co-production modules, for example water-gas-shift and Fischer-Tropsch catalysts, are readily poisoned by hydrogen sulfide (H{sub 2}S), a sulfur contaminant, present in the coal-derived fuel gases. To prevent poisoning of these catalysts, the removal of H{sub 2}S down to the parts-per-billion level is necessary. Historically, research into the purification of coal-derived fuel gases has focused on dry technologies that offer the prospect of higher combined cycle efficiencies as well as improved thermal integration with co-production modules. Primarily, these concepts rely on a highly selective process separation step to remove low concentrations of H{sub 2}S present in the fuel gases and produce a concentrated stream of sulfur bearing effluent. This effluent must then undergo further processing to be converted to its final form, usually elemental sulfur. Ultimately, desulfurization of coal-derived fuel gases may cost as much as 15% of the total fixed capital investment (Chen et al., 1992). It is, therefore, desirable to develop new technology that can accomplish H{sub 2}S separation and direct conversion to elemental sulfur more efficiently and with a lower initial fixed capital investment.

Gardner, Todd H.; Berry, David A.; Lyons, K. David; Beer, Stephen K.; Monahan, Michael J.

2001-11-06T23:59:59.000Z

13

Flash hydrogenation of coal  

DOE Patents (OSTI)

A process for the hydrogenation of coal comprising the contacting of powdered coal with hydrogen in a rotating fluidized bed reactor. A rotating fluidized bed reactor suitable for use in this process is also disclosed. The coal residence time in the reactor is limited to less than 5 seconds while the hydrogen contact time is not in excess of 0.2 seconds.

Manowitz, Bernard (Brightwaters, NY); Steinberg, Meyer (Huntington Station, NY); Sheehan, Thomas V. (Hampton Bays, NY); Winsche, Warren E. (Bellport, NY); Raseman, Chad J. (Setauket, NY)

1976-01-01T23:59:59.000Z

14

Initiators of coal hydrogenation  

Science Conference Proceedings (OSTI)

The results are given of an investigation of the influence of additions of certain organosilicon compounds of cyclic and linear nature on the coal hydrogenation process.

Krichko, A.A.; Dembovskaya, E.A.; Gorlov, E.G.

1983-01-01T23:59:59.000Z

15

Initiators of coal hydrogenation  

Science Conference Proceedings (OSTI)

The initiators examined include cyclic and linear silico-organic compounds, the effects of which on the hydrogenation process are studied. The substances not only localize the active radicals before these are stabilised by hydrogen, but actually activate the destruction reaction of the coal substance and in this way generate atomic hydrogen: radical polymerization inhibitors thus convert to activators and hydrogen transfer. (8 refs.)

Krichko, A.A.; Dembovskaya, E.A.; Gorlov, E.G.

1983-01-01T23:59:59.000Z

16

Metallic Membrane Materials Development for Hydrogen Production from Coal Derived Syngas  

DOE Green Energy (OSTI)

The goals of Office of Clean Coal are: (1) Improved energy security; (2) Reduced green house gas emissions; (3) High tech job creation; and (4) Reduced energy costs. The goals of the Hydrogen from Coal Program are: (1) Prove the feasibility of a 40% efficient, near zero emissions IGCC plant that uses membrane separation technology and other advanced technologies to reduce the cost of electricity by at least 35%; and (2) Develop H{sub 2} production and processing technologies that will contribute {approx}3% in improved efficiency and 12% reduction in cost of electricity.

O.N. Dogan; B.H. Howard; D.E. Alman

2012-02-26T23:59:59.000Z

17

Process for hydrogenating coal and coal solvents  

SciTech Connect

A novel process is described for the hydrogenation of coal by the hydrogenation of a solvent for the coal in which the hydrogenation of the coal solvent is conducted in the presence of a solvent hydrogenation catalyst of increased activity, wherein the hydrogenation catalyst is produced by reacting ferric oxide with hydrogen sulfide at a temperature range of 260.degree. C. to 315.degree. C. in an inert atmosphere to produce an iron sulfide hydrogenation catalyst for the solvent. Optimally, the reaction temperature is 275.degree. C. Alternately, the reaction can be conducted in a hydrogen atmosphere at 350.degree. C.

Tarrer, Arthur R. (Auburn, AL); Shridharani, Ketan G. (Auburn, AL)

1983-01-01T23:59:59.000Z

18

PALLADIUM/COPPER ALLOY COMPOSITE MEMBRANES FOR HIGH TEMPERATURE HYDROGEN SEPARATION FROM COAL-DERIVED GAS STREAMS  

DOE Green Energy (OSTI)

For hydrogen from coal gasification to be used economically, processing approaches that produce a high purity gas must be developed. Palladium and its alloys, nickel, platinum and the metals in Groups 3 to 5 of the Periodic Table are all permeable to hydrogen. Hydrogen permeable metal membranes made of palladium and its alloys are the most widely studied due to their high hydrogen permeability, chemical compatibility with many hydrocarbon containing gas streams, and infinite hydrogen selectivity. Our Pd composite membranes have demonstrated stable operation at 450 C for over 70 days. Coal derived synthesis gas will contain up to 15000 ppm H{sub 2}S as well as CO, CO{sub 2}, N{sub 2} and other gases. Highly selectivity membranes are necessary to reduce the H{sub 2}S concentration to acceptable levels for solid oxide and other fuel cell systems. Pure Pd-membranes are poisoned by sulfur, and suffer from mechanical problems caused by thermal cycling and hydrogen embrittlement. Recent advances have shown that Pd-Cu composite membranes are not susceptible to the mechanical, embrittlement, and poisoning problems that have prevented widespread industrial use of Pd for high temperature H{sub 2} separation. These membranes consist of a thin ({le} 5 {micro}m) film of metal deposited on the inner surface of a porous metal or ceramic tube. With support from this DOE Grant, we have fabricated thin, high flux Pd-Cu alloy composite membranes using a sequential electroless plating approach. Thin, Pd{sub 60}Cu{sub 40} films exhibit a hydrogen flux more than ten times larger than commercial polymer membranes for H{sub 2} separation, resist poisoning by H{sub 2}S and other sulfur compounds typical of coal gas, and exceed the DOE Fossil Energy target hydrogen flux of 80 ml/cm{sup 2} {center_dot} min = 0.6 mol/m{sup 2} {center_dot} s for a feed pressure of 40 psig. Similar Pd-membranes have been operated at temperatures as high as 750 C. We have developed practical electroless plating procedures for fabrication of thin Pd-Cu composite membranes at any scale.

J. Douglas Way

2003-01-01T23:59:59.000Z

19

NETL: Coal & Coal Biomass to Liquids - Alternate Hydrogen Production  

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

Coal and CoalBiomass to Liquids Alternate Hydrogen Production In the Alternate Production technology pathway, clean syngas from coal is converted to high-hydrogen-content liquid...

20

Production of High-Hydrogen Content Coal-Derived Liquids [Part 3 of 3  

Science Conference Proceedings (OSTI)

The primary goal of this project has been to evaluate and compare the effect of the intrinsic differences between cobalt (Co) and iron (Fe) catalysts for Fischer-Tropsch (FT) synthesis using coal-derived syngas. Crude oil, especially heavy, high-sulfur crude, is no longer the appropriate source for the additional, or marginal, amounts of middle-distillate fuels needed to meet growing US and world demand for diesel and jet fuels. Only about 1/3 of the marginal crude oil barrel can be made into diesel and jet fuels. The remaining 2/3 contributes further to global surpluses of by-products. FT can produce these needed marginal, low-sulfur middle-distillate fuels more efficiently, with less environmental impact, and from abundant US domestic resources. Cobalt FT catalyst is more efficient, and less expensive overall, than iron FT catalyst. Mechanisms of cobalt FT catalyst functioning, and poisoning, have been elucidated. Each of these primary findings is amplified by several secondary findings, and these are presented, and verified in detail. The most effective step the United States can take to begin building toward improved long-term national energy security, and to reduce dependence, over time, on imported crude oil from unfriendly and increasingly unstable areas of the world, is to begin producing additional, or marginal amounts of, middle-distillate-type fuels, such as ultralow sulfur diesel (ULSD) and jet fuel (not gasoline) from US domestic resources other than petroleum. FT synthesis of these middle distillate fuels offers the advantage of being able to use abundant and affordable US coal and biomass as the primary feedstocks. Use of the cobalt FT catalyst system has been shown conclusively to be more effective and less expensive than the use of iron FT catalyst with syngas derived from coal, or from coal and biomass combined. This finding is demonstrated in detail for the initial case of a relatively small FT plant of about 2000 barrels per day based upon coal and biomass. The primary feature of such a plant, in the current situation in which no commercial FT plants are operating in the US, is that it requires a relatively modest capital investment, meaning that such a plant could actually be built, operated, and replicated in the near term. This is in contrast to the several-billion dollar investment, and accompanying risk, that would be required for a plant of more than an order of magnitude greater capacity, which has been referred to in the technical literature on fuel production as the capacity required to be considered "commercial-scale." The effects of more than ten different potential poisons for cobalt FT catalyst have been studied extensively and in detail using laboratory continuous-stirred tank reactors (CSTRs) and bottled laboratory syngas "spiked" with precisely controlled amounts of the poisons, typically at the levels of 10s or 100s of parts per billion. This data set has been generated and interpreted by world-renowned experts on FT catalysis at the University of Kentucky Center for Applied Energy Research (UK-CAER), and has enabled unprecedented insight regarding the many molecular-scale mechanisms that can play a role in the "poisoning" of cobalt FT catalyst.

Stephen Bergin

2011-03-30T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

Production of High-Hydrogen Content Coal-Derived Liquids [Part 2 of 3  

SciTech Connect

The primary goal of this project has been to evaluate and compare the effect of the intrinsic differences between cobalt (Co) and iron (Fe) catalysts for Fischer-Tropsch (FT) synthesis using coal-derived syngas. Crude oil, especially heavy, high-sulfur crude, is no longer the appropriate source for the additional, or marginal, amounts of middle-distillate fuels needed to meet growing US and world demand for diesel and jet fuels. Only about 1/3 of the marginal crude oil barrel can be made into diesel and jet fuels. The remaining 2/3 contributes further to global surpluses of by-products. FT can produce these needed marginal, low-sulfur middle-distillate fuels more efficiently, with less environmental impact, and from abundant US domestic resources. Cobalt FT catalyst is more efficient, and less expensive overall, than iron FT catalyst. Mechanisms of cobalt FT catalyst functioning, and poisoning, have been elucidated. Each of these primary findings is amplified by several secondary findings, and these are presented, and verified in detail. The most effective step the United States can take to begin building toward improved long-term national energy security, and to reduce dependence, over time, on imported crude oil from unfriendly and increasingly unstable areas of the world, is to begin producing additional, or marginal amounts of, middle-distillate-type fuels, such as ultralow sulfur diesel (ULSD) and jet fuel (not gasoline) from US domestic resources other than petroleum. FT synthesis of these middle distillate fuels offers the advantage of being able to use abundant and affordable US coal and biomass as the primary feedstocks. Use of the cobalt FT catalyst system has been shown conclusively to be more effective and less expensive than the use of iron FT catalyst with syngas derived from coal, or from coal and biomass combined. This finding is demonstrated in detail for the initial case of a relatively small FT plant of about 2000 barrels per day based upon coal and biomass. The primary feature of such a plant, in the current situation in which no commercial FT plants are operating in the US, is that it requires a relatively modest capital investment, meaning that such a plant could actually be built, operated, and replicated in the near term. This is in contrast to the several-billion dollar investment, and accompanying risk, that would be required for a plant of more than an order of magnitude greater capacity, which has been referred to in the technical literature on fuel production as the capacity required to be considered "commercial-scale." The effects of more than ten different potential poisons for cobalt FT catalyst have been studied extensively and in detail using laboratory continuous-stirred tank reactors (CSTRs) and bottled laboratory syngas "spiked" with precisely controlled amounts of the poisons, typically at the levels of 10s or 100s of parts per billion. This data set has been generated and interpreted by world-renowned experts on FT catalysis at the University of Kentucky Center for Applied Energy Research (UK-CAER), and has enabled unprecedented insight regarding the many molecular-scale mechanisms that can play a role in the "poisoning" of cobalt FT catalyst.

Stephen Bergin

2011-03-30T23:59:59.000Z

22

Production of High-Hydrogen Content Coal-Derived Liquids [Part 1 of 3  

Science Conference Proceedings (OSTI)

The primary goal of this project has been to evaluate and compare the effect of the intrinsic differences between cobalt (Co) and iron (Fe) catalysts for Fischer-Tropsch (FT) synthesis using coal-derived syngas. Crude oil, especially heavy, high-sulfur crude, is no longer the appropriate source for the additional, or marginal, amounts of middle-distillate fuels needed to meet growing US and world demand for diesel and jet fuels. Only about 1/3 of the marginal crude oil barrel can be made into diesel and jet fuels. The remaining 2/3 contributes further to global surpluses of by-products. FT can produce these needed marginal, low-sulfur middle-distillate fuels more efficiently, with less environmental impact, and from abundant US domestic resources. Cobalt FT catalyst is more efficient, and less expensive overall, than iron FT catalyst. Mechanisms of cobalt FT catalyst functioning, and poisoning, have been elucidated. Each of these primary findings is amplified by several secondary findings, and these are presented, and verified in detail. The most effective step the United States can take to begin building toward improved long-term national energy security, and to reduce dependence, over time, on imported crude oil from unfriendly and increasingly unstable areas of the world, is to begin producing additional, or marginal amounts of, middle-distillate-type fuels, such as ultralow sulfur diesel (ULSD) and jet fuel (not gasoline) from US domestic resources other than petroleum. FT synthesis of these middle distillate fuels offers the advantage of being able to use abundant and affordable US coal and biomass as the primary feedstocks. Use of the cobalt FT catalyst system has been shown conclusively to be more effective and less expensive than the use of iron FT catalyst with syngas derived from coal, or from coal and biomass combined. This finding is demonstrated in detail for the initial case of a relatively small FT plant of about 2000 barrels per day based upon coal and biomass. The primary feature of such a plant, in the current situation in which no commercial FT plants are operating in the US, is that it requires a relatively modest capital investment, meaning that such a plant could actually be built, operated, and replicated in the near term. This is in contrast to the several-billion dollar investment, and accompanying risk, that would be required for a plant of more than an order of magnitude greater capacity, which has been referred to in the technical literature on fuel production as the capacity required to be considered "commercial-scale." The effects of more than ten different potential poisons for cobalt FT catalyst have been studied extensively and in detail using laboratory continuous-stirred tank reactors (CSTRs) and bottled laboratory syngas "spiked" with precisely controlled amounts of the poisons, typically at the levels of 10s or 100s of parts per billion. This data set has been generated and interpreted by world-renowned experts on FT catalysis at the University of Kentucky Center for Applied Energy Research (UK-CAER), and has enabled unprecedented insight regarding the many molecular-scale mechanisms that can play a role in the "poisoning" of cobalt FT catalyst.

Stephen Bergin

2011-03-30T23:59:59.000Z

23

HYDROGEN FROM COAL  

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

MT R 20 0 2- 31 M itr et ek T ec h n ic a l Pap e r HYDROGEN FROM COAL November 2001 D. Gray G. Tomlinson JULY 2002 ii Customer: U.S. DOE NETL Contract No.: DE-AM26-99FT40465 Dept....

24

Effect of Impurities in Coal-Derived Syngas on Hydrogen Separation ...  

Science Conference Proceedings (OSTI)

The U.S. Department of Energy has established a set of performance targets for hydrogen separation membranes for the syngas applications in its Hydrogen...

25

Coal liquefaction and hydrogenation  

SciTech Connect

The coal liquefaction process disclosed uses three stages. The first stage is a liquefaction. The second and third stages are hydrogenation stages at different temperatures and in parallel or in series. One stage is within 650.degree.-795.degree. F. and optimizes solvent production. The other stage is within 800.degree.-840.degree. F. and optimizes the C.sub.5 -850.degree. F. product.

Schindler, Harvey D. (Fair Lawn, NJ)

1985-01-01T23:59:59.000Z

26

Robust Low-Cost Water-Gas Shift Membrane Reactor for High-Purity Hydrogen Production form Coal-Derived Syngas  

DOE Green Energy (OSTI)

This report details work performed in an effort to develop a low-cost, robust water gas shift membrane reactor to convert coal-derived syngas into high purity hydrogen. A sulfur- and halide-tolerant water gas shift catalyst and a sulfur-tolerant dense metallic hydrogen-permeable membrane were developed. The materials were integrated into a water gas shift membrane reactor in order to demonstrate the production of >99.97% pure hydrogen from a simulated coal-derived syngas stream containing 2000 ppm hydrogen sulfide. The objectives of the program were to (1) develop a contaminant-tolerant water gas shift catalyst that is able to achieve equilibrium carbon monoxide conversion at high space velocity and low steam to carbon monoxide ratio, (2) develop a contaminant-tolerant hydrogen-permeable membrane with a higher permeability than palladium, (3) demonstrate 1 L/h purified hydrogen production from coal-derived syngas in an integrated catalytic membrane reactor, and (4) conduct a cost analysis of the developed technology.

James Torkelson; Neng Ye; Zhijiang Li; Decio Coutinho; Mark Fokema

2008-05-31T23:59:59.000Z

27

Hydrogen from Coal Edward Schmetz  

E-Print Network (OSTI)

gasification technology assumes advanced E-gas gasification. · RD&D is estimated to reduce the cost of hydrogenGenFutureGen Hydrogen Fuel Initiative Hydrogen Fuel Initiative Gasification Fuel Cells Turbines Gasification Fuel Cells-production plant · Hydrogen from Coal Program will coordinate with associated DOE programs in Gasification, Fuel

28

HYDROGEN FROM COAL  

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

MT MT R 20 0 2- 31 M itr et ek T ec h n ic a l Pap e r HYDROGEN FROM COAL November 2001 D. Gray G. Tomlinson JULY 2002 ii Customer: U.S. DOE NETL Contract No.: DE-AM26-99FT40465 Dept. No.: H050 Project No.: 0601CTC2-C2 Center for Science and Technology Innovative Technology in the Public Interest (tm) iii Disclaimer This report was prepared as an account of work sponsored by an agency of the United States (U.S.) government. Neither the U.S., nor any agency thereof, nor any of their employees, nor any of their contractors, subcontractors, or their employees makes any warranty, expressed or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference

29

Coal liquefaction and hydrogenation  

DOE Patents (OSTI)

Disclosed is a coal liquefaction process using two stages. The first stage liquefies the coal and maximizes the product while the second stage hydrocracks the remainder of the coal liquid to produce solvent.

Schindler, Harvey D. (Fair Lawn, NJ); Chen, James M. (Edison, NJ)

1985-01-01T23:59:59.000Z

30

NETL: Coal & Coal Biomass to Liquids - Hydrogen and Clean Fuels...  

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

of hydrogen and nitrogen. CLICK ON IMAGE TO SEE LARGER VIEW Hydrogen is produced from coal in a process that is similar to SMR but more complex because coal is not a single...

31

Hydrogen Resource Assessment: Hydrogen Potential from Coal, Natural...  

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

2009 Hydrogen Resource Assessment Hydrogen Potential from Coal, Natural Gas, Nuclear, and Hydro Power Anelia Milbrandt and Margaret Mann National Renewable Energy Laboratory 1617...

32

NETL: Coal & Coal Biomass to Liquids - Hydrogen and Clean Fuels...  

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

Strategies Central Hydrogen Production Coal Supply Regions CLICK ON IMAGE TO SEE LARGER VIEW Coal is a plentiful domestic resource, and is available in several major regions of the...

33

Partial Oxidation Gas Turbine for Power and Hydrogen Co-Production from Coal-Derived Fuel in Industrial Applications  

SciTech Connect

The report presents a feasibility study of a new type of gas turbine. A partial oxidation gas turbine (POGT) shows potential for really high efficiency power generation and ultra low emissions. There are two main features that distinguish a POGT from a conventional gas turbine. These are associated with the design arrangement and the thermodynamic processes used in operation. A primary design difference of the POGT is utilization of a non?catalytic partial oxidation reactor (POR) in place of a conventional combustor. Another important distinction is that a much smaller compressor is required, one that typically supplies less than half of the air flow required in a conventional gas turbine. From an operational and thermodynamic point of view a key distinguishing feature is that the working fluid, fuel gas provided by the OR, has a much higher specific heat than lean combustion products and more energy per unit mass of fluid can be extracted by the POGT expander than in the conventional systems. The POGT exhaust stream contains unreacted fuel that can be combusted in different bottoming ycle or used as syngas for hydrogen or other chemicals production. POGT studies include feasibility design for conversion a conventional turbine to POGT duty, and system analyses of POGT based units for production of power solely, and combined production of power and yngas/hydrogen for different applications. Retrofit design study was completed for three engines, SGT 800, SGT 400, and SGT 100, and includes: replacing the combustor with the POR, compressor downsizing for about 50% design flow rate, generator replacement with 60 90% ower output increase, and overall unit integration, and extensive testing. POGT performances for four turbines with power output up to 350 MW in POGT mode were calculated. With a POGT as the topping cycle for power generation systems, the power output from the POGT ould be increased up to 90% compared to conventional engine keeping hot section temperatures, pressures, and volumetric flows practically identical. In POGT mode, the turbine specific power (turbine net power per lb mass flow from expander exhaust) is twice the value of the onventional turbine. POGT based IGCC plant conceptual design was developed and major components have been identified. Fuel flexible fluid bed gasifier, and novel POGT unit are the key components of the 100 MW IGCC plant for co producing electricity, hydrogen and/or yngas. Plant performances were calculated for bituminous coal and oxygen blown versions. Various POGT based, natural gas fueled systems for production of electricity only, coproduction of electricity and hydrogen, and co production of electricity and syngas for gas to liquid and hemical processes were developed and evaluated. Performance calculations for several versions of these systems were conducted. 64.6 % LHV efficiency for fuel to electricity in combined cycle was achieved. Such a high efficiency arise from using of syngas from POGT exhaust s a fuel that can provide required temperature level for superheated steam generation in HRSG, as well as combustion air preheating. Studies of POGT materials and combustion instabilities in POR were conducted and results reported. Preliminary market assessment was performed, and recommendations for POGT systems applications in oil industry were defined. POGT technology is ready to proceed to the engineering prototype stage, which is recommended.

Joseph Rabovitser

2009-06-30T23:59:59.000Z

34

DOE Hydrogen Analysis Repository: Production of Hydrogen from Coal  

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

Production of Hydrogen from Coal Production of Hydrogen from Coal Project Summary Full Title: Production of High Purity Hydrogen from Domestic Coal: Assessing the Techno-Economic Impact of Emerging Technologies Project ID: 265 Principal Investigator: Kristin Gerdes Brief Description: This report assesses the improvements in cost and performance of hydrogen production from domestic coal when employing emerging technologies funded by DOE. Keywords: Hydrogen production; Coal Purpose This analysis specifically evaluates replacing conventional acid gas removal (AGR) and hydrogen purification with warm gas cleanup (WGCU) and a high-temperature hydrogen membrane (HTHM) that meets DOE's 2010 and 2015 performance and cost research and development (R&D) targets. Performer Principal Investigator: Kristin Gerdes

35

Production of Hydrogen from Underground Coal Gasification  

DOE Patents (OSTI)

A system of obtaining hydrogen from a coal seam by providing a production well that extends into the coal seam; positioning a conduit in the production well leaving an annulus between the conduit and the coal gasification production well, the conduit having a wall; closing the annulus at the lower end to seal it from the coal gasification cavity and the syngas; providing at least a portion of the wall with a bifunctional membrane that serves the dual purpose of providing a catalyzing reaction and selectively allowing hydrogen to pass through the wall and into the annulus; and producing the hydrogen through the annulus.

Upadhye, Ravindra S. (Pleasanton, CA)

2008-10-07T23:59:59.000Z

36

Hydrogen from Coal | Department of Energy  

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

Liquids » Hydrogen Liquids » Hydrogen from Coal Hydrogen from Coal Technicians make adjustments to equipment in the hydrogen membrane testing unit at FE's National Energy Technology Laboratory. NETL researchers in the Office of Research and Development are testing different types of materials that might be used to separate hydrogen from other gases. Photo courtesy of NETL. Technicians make adjustments to equipment in the hydrogen membrane testing unit at FE's National Energy Technology Laboratory. NETL researchers in the Office of Research and Development are testing different types of materials that might be used to separate hydrogen from other gases. Photo courtesy of NETL. Hydrogen from coal research supports goals of increasing energy security, reducing environmental impact of energy use, promoting economic

37

COST-EFFECTIVE METHOD FOR PRODUCING SELF SUPPORTED PALLADIUM ALLOY MEMBRANES FOR USE IN EFFICIENT PRODUCTION OF COAL DERIVED HYDROGEN  

DOE Green Energy (OSTI)

Over the last quarter, we developed procedures for producing free-standing, defect free films using rigid silicon and glass substrates over areas up to 12 square inches. Since formation of contiguous Pd-Cu films in the 2-3 {micro}m-thick range is ultimately governed by the size of the particle contamination on the supporting substrate surface, we have adopted techniques utilized by the semiconductor industry to reduce and eventually eliminate particle contamination. We have found these techniques to be much more effective on rigid substrates and have made a down select decision on removal methods (a key milestone) based on these results and the performance of membranes fabricated by this technique. The path to fabricating even larger membranes is straightforward and will be demonstrated in the coming months. Hydrogen permeation tests were also conducted this quarter on as-deposited, Pd-Cu membranes, between 6-14 {micro}m-thick. In the case of a 6 {micro}m-thick film, the pure hydrogen flux at 20 psig and {approx}260 C was 36 cm{sup 3}(STP)/cm{sup 2} min. This flux corresponds to a pure hydrogen permeability of 7.4 {center_dot} 10{sup -5} cm{sup 3} cm cm{sup -2} s{sup -1} cm Hg{sup -1/2} at 250 C. This value is within 20% of the pure hydrogen permeability at 250 C reported in the McKinley patent. In the case of a 14 {micro}m-thick membrane tested at 350 C, the pure hydrogen flux, measured before initiating a pinhole-size leak, was 2.1 {center_dot} 10{sup -5} cm{sup 3}(STP) {center_dot} cm/cm{sup 2} {center_dot} s {center_dot} cm Hg{sup 0.5}. This value is considerably lower than the expected permeability of Pd{sub 60}Cu{sub 40} materials at 400 C. To date, essentially all of the sputtered deposited Pd-Cu thin film membranes have had palladium compositions that were as much as 3% greater than the ideal 60 weight percent composition (this is a direct consequence of sputtering from a 60/40, Pd/Cu alloy target). As the concentration of Pd is increased beyond the optimum 60% value, a less desirable two-phase structure forms at the higher temperatures (in this case, above 260-280 C). As we continue development of procedures for producing thinner Pd-Cu films next quarter, we will also be optimizing alloy composition and corresponding hydrogen permeation flux as well.

B. Lanning; J. Arps

2005-01-28T23:59:59.000Z

38

COST-EFFECTIVE METHOD FOR PRODUCING SELF SUPPORTED PALLADIUM ALLOY MEMBRANES FOR USE IN EFFICIENT PRODUCTION OF COAL DERIVED HYDROGEN  

DOE Green Energy (OSTI)

Over the last quarter, we continued to optimize procedures for producing free-standing, defect free films using rigid silicon and glass substrates. A strong correlation was observed between sputter power and formation of defects (pinholes) in the film; i.e., lower power, and correspondingly lower deposition rate, results in a lower defect density. Films less than 1 {micro}m-thick have been successfully released from both silicon and glass substrates although the minimum thickness for pinhole-free films over a 4-inch diameter disc is still on the order of 3-4 {micro}m. Results from hydrogen permeation testing over the last quarter have shown a marked increase in membrane performance primarily due to proper alloy composition and pre-treatment procedures. As an example, the hydrogen flux at 400 C and 20 psi trans-membrane pressure, for a 5 {micro}m-thick membrane, was 120 cm{sup 3} (STP)/cm{sup 2} min. The productivity of this membrane exceeds the 2015 DOE Fossil Energy targets. Hydrogen permeability was calculated to be 2.0 {center_dot} 10{sup -4} cm{sup 3}(STP) {center_dot} cm/cm{sup 2} {center_dot} s {center_dot} cm Hg{sup 0.5}. Permeation tests were then repeated on a sibling membrane sample and the measured hydrogen flow rate at 400 C and 20 psi was 58 cm{sup 3} (STP)/min. Although lower than the flow rate of the first sample, the hydrogen flow rate increased to 175 cm{sup 3} (STP)/min after two oxidation treatments. Finally, with the attendance of John Shen and the rest of the program team members at the IdaTech facility in Bend, OR, we presented an overview of program activities. Subsequently, we prepared detailed written responses to John Shen's questions with regard to technical feasibility, maturity, scale-up and commercialization potential in comparison to competing hydrogen separation methods such as pressure swing absorption and ionic conducting membranes.

B. Lanning; J. Arps

2005-04-01T23:59:59.000Z

39

Coal hydrogenation and deashing in ebullated bed catalytic reactor  

SciTech Connect

An improved process for hydrogenation of coal containing ash with agglomeration and removal of ash from an ebullated bed catalytic reactor to produce deashed hydrocarbon liquid and gas products. In the process, a flowable coal-oil slurry is reacted with hydrogen in an ebullated catalyst bed reaction zone at elevated temperature and pressure conditions. The upward velocity and viscosity of the reactor liquid are controlled so that a substantial portion of the ash released from the coal is agglomerated to form larger particles in the upper portion of the reactor above the catalyst bed, from which the agglomerated ash is separately withdrawn along with adhering reaction zone liquid. The resulting hydrogenated hydrocarbon effluent material product is phase separated to remove vapor fractions, after which any ash remaining in the liquid fraction can be removed to produce substantially ash-free coal-derived liquid products.

Huibers, Derk T. A. (Pennington, NJ); Johanson, Edwin S. (Princeton, NJ)

1983-01-01T23:59:59.000Z

40

COST-EFFECTIVE METHOD FOR PRODUCING SELF SUPPORTED PALLADIUM ALLOY MEMBRANES FOR USE IN EFFICIENT PRODUCTION OF COAL DERIVED HYDROGEN  

DOE Green Energy (OSTI)

During the last quarter, new procedures were developed and implemented to improve reliability and repeatability of release characteristics from the temporary substrate (i.e., silicon wafer) and to minimize through-thickness defects in a 6-inch diameter film, 3 microns in thickness. With the new procedures, we have been able to consistently produce essentially stress free films, with zero or minimal defects (less than 5) across a 6-inch diameter area. (It is important to note that for those films containing pinholes, a procedure has been developed to repair the pinholes to form a gas tight seal). The films are all within the identified tolerance range for composition (i.e., 60 {+-} 0.2 % Pd). A number of these films have subsequently been shipped to IdaTech for evaluation and integration into their test module. Colorado School of Mines continued their high temperature evaluation of 6 micron thick, sputtered Pd-Cu films. Pure hydrogen permeability increased up to 400 C while the membrane was in the {beta}-phase and dropped once the temperature increased to over 450 C. Above this temperature, as confirmed by the binary phase diagram, the film transforms into either a mixed {alpha}/{beta} or pure {alpha} phase. The same trend was observed for a baseline 25 micron-thick foil (from Wilkinson) where the pure hydrogen permeability increased with temperature while the membrane was in the {beta}-phase and then decreased upon transformation to the {alpha} phase.

B. Lanning; J. Arps

2005-10-28T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

COST-EFFECTIVE METHOD FOR PRODUCING SELF SUPPORTED PALLADIUM ALLOY MEMBRANES FOR USE IN EFFICIENT PRODUCTION OF COAL DERIVED HYDROGEN  

DOE Green Energy (OSTI)

In the past quarter, significant progress has been made in optimize the deposition and release characteristics of ultrathin (less than 4 micron) membranes from rigid silicon substrates. Specifically, we have conducted a series of statistically designed experiments to examine the effects of plasma cleaning and compliant layer deposition conditions on the stress, release and pinhole density of membranes deposited on 4 inch and 6 inch round substrates. With this information we have progressed to the deposition and release of ultra-thin membranes from 12-inch diameter (113 sq. in.) rigid substrates, achieving a key milestone for large-area membrane fabrication. Idatech received and is beginning preparations to test the Pd alloy membranes fabricated at SwRI the previous quarter. They are currently evaluating alternate gasketing methods and support materials that will allow for effective sealing and mounting of such thin membranes. David Edlund has also recently left Idatech and Bill Pledger (Chief Engineer) has replaced him as the primary technical point of contact. At Idetech's request a small number of additional 16 sq. in, samples were provided in a 2 in. by 8 in. geometry for use in a new module design currently under development. Recent work at the Colorado School of Mines has focused on developing preconditioning methods for thin Pd alloy membranes (6 microns or less) and continuing tests of thin membranes produced at SwRI. Of particular note, a 300-hour short-term durability study was completed over a range of temperatures from 300-450 C on a foil that showed perfect hydrogen selectivity throughout the entire test. With a 20 psi driving force, pure hydrogen flow rates ranged from 500 to 700 cc/min. Calculated at DOE specified conditions, the H{sub 2} flux of this membrane exceeded the 2010 Fossil target value of 200 SCFH/ft{sup 2}.

J. Arps

2006-01-01T23:59:59.000Z

42

COST-EFFECTIVE METHOD FOR PRODUCING SELF SUPPORTED PALLADIUM ALLOY MEMBRANES FOR USE IN EFFICIENT PRODUCTION OF COAL DERIVED HYDROGEN  

DOE Green Energy (OSTI)

In continuation of efforts from last quarter, processing parameters, used in the formation of Pd-Cu alloy films, were being optimized in a drum (web) coater system with the goal of producing large-area, contiguous, pinhole-free films for H{sub 2} separation membranes. Since the (pre-treatment) functionality of the surface of the plastic backing material is sub-optimal, they tended to produce films in the drum coater that were either not contiguous (disseminates upon release from the polymer backing material) or contain pinholes. Alternative approaches, such as direct deposition onto thermally oxidized silicon wafers, have been attempted to yield pinhole-free films; i.e., formation of a poorly adherent Pd-Cu film on silicon will then directly release from the silicon substrate. Permeation characteristics of a 25 {micro}m-thick, Pd{sub 60}Cu{sub 40} alloy foil were conducted. After pre-treating the sample to stabilize the FCC {beta}-phase, the hydrogen permeability was determined to be 5.4 x 10{sup -5} cm{sup 3} cmcm{sup -2}s{sup -1}cm Hg{sup -1/2}. Thin, 1-3 {micro}m-thick Pd-Cu alloy films have been prepared on PS films and samples will be prepared and tested in the next quarter.

B. Lanning; J. Arps

2004-07-01T23:59:59.000Z

43

Hydrogen-donor coal liquefaction process  

DOE Patents (OSTI)

Improved liquid yields are obtained during the hydrogen-donor solvent liquefaction of coal and similar carbonaceous solids by maintaining a higher concentration of material having hydrogenation catalytic activity in the downstream section of the liquefaction reactor system than in the upstream section of the system.

Wilson, Jr., Edward L. (Baytown, TX); Mitchell, Willard N. (Baytown, TX)

1980-01-01T23:59:59.000Z

44

Materials in Clean Power Systems VI: Clean Coal-, Hydrogen Based ...  

Science Conference Proceedings (OSTI)

clean coal technologies, carbon sequestration, membrane-based gas separations, biofuel production, hydrogen production from various sources, etc. With an...

45

Chemicals from coal. Utilization of coal-derived phenolic compounds  

Science Conference Proceedings (OSTI)

This article provides an overview for possible utilization of coal-derived phenolic compounds. Phenolic compounds are abundant in coal-derived liquids. Coal-derived phenolic compounds include phenol, cresol, catechol, methylcatechol, naphthol, and their derivatives. Liquids from coal liquefaction, pyrolysis, gasification, and carbonization are potential sources of phenolic chemicals, although certain processing and separation are needed. There are opportunities for coal-based phenolic chemicals, because there are existing industrial applications and potential new applications. Currently the petrochemical industry produces phenol in multi-step processes, and new research and development has resulted in a one-step process. Selective methylation of phenol can produce a precursor for aromatic engineering plastics. Catalytic oxidation of phenol has been commercialized recently for catechol production. There are potential new uses of phenol that could replace large-volume multi-step chemical processes that are based on benzene as the starting material. New chemical research on coal and coal-derived liquids can pave the way for their non-fuel uses for making chemicals and materials.

Song, C.; Schobert, H.H.

1999-07-01T23:59:59.000Z

46

High-Temperature Nano-Derived Micro-Hydrogen Sulfide Sensors  

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

Temperature Nano-Derived Micro- Temperature Nano-Derived Micro- Hydrogen and -Hydrogen Sulfide Sensors Background The Department of Energy (DOE) National Energy Technology Laboratory (NETL) seeks applications for the University Coal Research (UCR) Program to further develop the understanding of coal utilization. Since the program's inception in 1979, its primary objectives have been to (1) improve our understanding of the chemical and physical processes involved in the conversion and utilization of coal in an environmentally

47

Process and apparatus for coal hydrogenation  

SciTech Connect

In a coal liquefaction process an aqueous slurry of coal is prepared containing a dissolved liquefaction catalyst. A small quantity of oil is added to the slurry and then coal-oil agglomerates are prepared by agitation of the slurry at atmospheric pressure. The resulting mixture is drained of excess water and dried at atmospheric pressure leaving catalyst deposited on the agglomerates. The agglomerates then are fed to an extrusion device where they are formed into a continuous ribbon of extrudate and fed into a hydrogenation reactor at elevated pressure and temperature. The catalytic hydrogenation converts the extrudate primarily to liquid hydrocarbons in the reactor. The liquid drained in recovering the agglomerates is recycled.

Ruether, John A. (McMurray, PA); Simpson, Theodore B. (McLean, VA)

1991-01-01T23:59:59.000Z

48

Hydrogen production with coal using a pulverization device  

DOE Patents (OSTI)

A method for producing hydrogen from coal is described wherein high temperature steam is brought into contact with coal in a pulverizer or fluid energy mill for effecting a steam-carbon reaction to provide for the generation of gaseous hydrogen. The high temperature steam is utilized to drive the coal particles into violent particle-to-particle contact for comminuting the particulates and thereby increasing the surface area of the coal particles for enhancing the productivity of the hydrogen.

Paulson, Leland E. (Morgantown, WV)

1989-01-01T23:59:59.000Z

49

Process and apparatus for coal hydrogenation  

DOE Patents (OSTI)

In a coal liquefaction process an aqueous slurry of coal is prepared containing a dissolved liquefaction catalyst. A small quantity of oil is added to the slurry and then coal-oil agglomerates are prepared by agitation of the slurry at atmospheric pressure. The resulting mixture of agglomerates, excess water, dissolved catalyst, and unagglomerated solids is pumped to reaction pressure and then passed through a drainage device where all but a small amount of surface water is removed from the agglomerates. Sufficient catalyst for the reaction is contained in surface water remaining on the agglomerates. The agglomerates fall into the liquefaction reactor countercurrently to a stream of hot gas which is utilized to dry and preheat the agglomerates as well as deposit catalyst on the agglomerates before they enter the reactor where they are converted to primarily liquid products under hydrogen pressure.

Ruether, John A. (McMurray, PA)

1988-01-01T23:59:59.000Z

50

CERAMIC MEMBRANES FOR HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

The preparation and performance of membranes for application to hydrogen separation from coal-derived gas is described. The membrane material investigated was dense amorphous silica deposited on a suitable support by chemical vapor deposition (CVD). Two types of support materials were pursued. One type consisted of a two-layer composite, zeolite silicalite/{alpha}-Al{sub 2}O{sub 3}, in the form of tubes approximately 0.7 cm in diameter. The other type was porous glass tubes of diameter below 0.2 cm. The first type of support was prepared starting from {alpha}-Al{sub 2}O{sub 3} tubes of 1{micro}m mean pore diameter and growing by hydrothermal reaction a zeolite silicalite layer inside the pores of the alumina at the OD side. After calcination to remove the organic template used in the hydrothermal reaction, CVD was carried out to deposit the final silica layer. CVD was carried out by alternating exposure of the surface with silicon tetrachloride and water vapor. SEM and N2 adsorption measurements were employed to characterize the membranes at several stages during their preparation. Permeation measurements of several gases yielded H{sub 2}:N{sub 2} ideal selectivity of 150-200 at room temperature declining to 110 at 250 C. The second type of support pursued was porous glass tubes prepared by a novel extrusion technique. A thick suspension of borosilicate glass powder in a polyethersulfone solution was extruded through a spinneret and after gelation the glass-polymer tube was heat treated to obtain a gas-tight glass tube. Leaching of the glass tube in hot water yielded connected pores with diameter on the order of 100 nm. CVD of the final silica layer was not carried out on these tubes on account of their large pore size.

George R. Gavalas

2004-04-01T23:59:59.000Z

51

A NOVEL MEMBRANE REACTOR FOR DIRECT HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

Gas Technology Institute is developing a novel concept of membrane reactor coupled with a gasifier for high efficiency, clean and low cost production of hydrogen from coal. The concept incorporates a hydrogen-selective membrane within a gasification reactor for direct extraction of hydrogen from coal-derived synthesis gases. The objective of this project is to determine the technical and economic feasibility of this concept by screening, testing and identifying potential candidate membranes under high temperature, high pressure, and harsh environments of the coal gasification conditions. The best performing membranes will be selected for preliminary reactor design and cost estimates. Hydrogen permeation data for several perovskite membranes BCN (BaCe{sub 0.9}Nd{sub 0.1}O{sub 3-x}), SCE (SrCe{sub 0.9}Eu{sub 0.1}O{sub 3}) and SCTm (SrCe{sub 0.95}Tm{sub 0.05}O{sub 3}) have been successfully obtained for temperatures between 800 and 950 C and pressures from 1 to 12 bar in this project. However, it is known that the cerate-based perovskite materials can react with CO{sub 2}. Therefore, the stability issue of the proton conducting perovskite materials under CO{sub 2} or H{sub 2}S environments was examined. Tests were conducted in the Thermo Gravimetric Analyzer (TGA) unit for powder and disk forms of BCN and SCE. Perovskite materials doped with zirconium (Zr) are known to be resistant to CO{sub 2}. The results from the evaluation of the chemical stability for the Zr doped perovskite membranes are presented. During this reporting period, flowsheet simulation was also performed to calculate material and energy balance based on several hydrogen production processes from coal using high temperature membrane reactor (1000 C), low temperature membrane reactor (250 C), or conventional technologies. The results show that the coal to hydrogen process employing both the high temperature and the low temperature membrane reactors can increase the hydrogen production efficiency (cold gas efficiency) by more than 50% compared to the conventional process. Using either high temperature or low temperature membrane reactor process also results in an increase of the cold gas efficiencies as well as the thermal efficiencies of the overall process.

Shain Doong; Estela Ong; Mike Atroshenko; Francis Lau; Mike Roberts

2005-07-29T23:59:59.000Z

52

Comparison of coal and iron requirements between bituminous coal hydrogenation and low temperature carbonization (L. T. C. ) followed by hydrogenation  

SciTech Connect

Plants producing 100,000 tons/yr aviation gasoline and 25,000 tons/yr of liquid petroleum gasoline (L.P.G.) by hydrogenation of coal and 100,000 tons/yr of aviation gasoline, 15,000 tons/yr L.P.G., and 912,000 tons/yr of excess L.T.C. coke by L.T.C. followed by hydrogenation of the L.T.C. tar are considered. Specific data are included on L.T.C., specific data for L.T.C. tar hydrogenation, and total coal requirement for L.T.C. of coal and hydrogenation of the L.T.C. tar. Information is also included on hydrogenation of bituminous coal and iron requirements. Three charts show differences between various bituminous coal conversion processes. The iron requirements for L.T.C. and tar hydrogenation was 100,500 tons and for bituminous coal hydrogenation it was 123,300 tons. An input of 1,480,000 tons of L.T.C. coal was calculated. The power coal requirement for L.T.C. and hydrogenation was 1,612,000 tons. The coal requirement for tar hydrogenation was 482,000 tons and 1,130,000 tons for surplus coke and gas. Therefore about 30% of the total coal was used for aviation gasoline and L.P.G. and about 70% for surplus coke and gas.

1943-04-21T23:59:59.000Z

53

Coal Electrolysis to Produce Hydrogen at Intermediate Temperatures.  

E-Print Network (OSTI)

??As an alternative technique for hydrogen production, coal electrolysis was evaluated at intermediate temperatures (80 C-108 C). First, an electrochemical technique was developed to (more)

Jin, Xin

2009-01-01T23:59:59.000Z

54

A NOVEL MEMBRANE REACTOR FOR DIRECT HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

Gas Technology Institute is developing a novel concept of membrane gasifier for high efficiency, clean and low cost production of hydrogen from coal. The concept incorporates a hydrogen-selective membrane within a gasification reactor for direct extraction of hydrogen from coal-derived synthesis gases. The objective of this project is to determine the technical and economic feasibility of this concept by screening, testing and identifying potential candidate membranes under high temperature, high pressure, and harsh environments of the coal gasification conditions. The best performing membranes will be selected for preliminary reactor design and cost estimates. To evaluate the performances of the candidate membranes under the gasification conditions, a high temperature/high pressure hydrogen permeation unit has been constructed in this project. During this reporting period, the unit has been fully commissioned and is operational. The unit is capable of operating at temperatures up to 1100 C and pressures to 60 atm for evaluation of ceramic membranes such as mixed ionic conducting membrane. A double-seal technique has been developed and tested successfully to achieve leak-tight seal for the membranes. Initial data for a commercial Palladium-Gold membrane were obtained at temperatures to 450 C and pressures to 13 atm. Tests for the perovskite membranes are being performed and the results will be reported in the next quarter. A membrane gasification reactor model was developed to consider the H{sub 2} permeability of the membrane, the kinetics and the equilibriums of the gas phase reactions in the gasifier, the operating conditions and the configurations of the membrane reactor. The results show that the hydrogen production efficiency using the novel membrane gasification reactor concept can be increased by about 50% versus the conventional gasification process. This confirms the previous evaluation results from the thermodynamic equilibrium calculation. A rigorous model for hydrogen permeation through mixed proton-electron conducting ceramic membranes was also developed based on non-equilibrium thermodynamics. The results from the simulation work confirm that the hydrogen flux increases with increasing partial pressure of hydrogen. The presence of steam in the permeate side can have a small negative effect on the hydrogen flux, in the order of 10%. When the steam partial pressure is greater than 1 atm, the hydrogen flux becomes independent of the steam pressure.

Shain Doong; Estela Ong; Mike Atroshenko; Francis Lau; Mike Roberts

2004-07-29T23:59:59.000Z

55

NETL: Gasification - Advanced Hydrogen Transport Membranes for Coal  

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

Syngas Processing Systems Syngas Processing Systems Advanced Hydrogen Transport Membranes for Coal Gasification Praxair Inc. Project Number: FE0004908 Project Description Praxair is conducting research to develop hydrogen transport membrane (HTM) technology to separate carbon dioxide (CO2) and hydrogen (H2) in coal-derived syngas for IGCC applications. The project team has fabricated palladium based membranes and measured hydrogen fluxes as a function of pressure, temperature, and membrane preparation conditions. Membranes are a commercially-available technology in the chemical industry for CO2 removal and H2 purification. There is, however, no commercial application of membrane processes that aims at CO2 capture for IGCC syngas. Due to the modular nature of the membrane process, the design does not exhibit economy of scale-the cost of the system will increase linearly as the plant system scale increases making the use of commercially available membranes, for an IGCC power plant, cost prohibitive. For a membrane process to be a viable CO2 capture technology for IGCC applications, a better overall performance is required, including higher permeability, higher selectivity, and lower membrane cost.

56

DOE Hydrogen Analysis Repository: Coal Distribution Constraints  

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

Coal Distribution Constraints Project Summary Full Title: Future Impacts of Coal Distribution Constraints on Coal Cost Project ID: 199 Principal Investigator: David McCollum...

57

Hydrotreating of coal-derived liquids  

SciTech Connect

The objective of Sandia`s refining of coal-derived liquids project is to determine the relationship between hydrotreating conditions and Product characteristics. The coal-derived liquids used in this work were produced In HTI`s first proof-of-concept run using Illinois No. 8 coal. Samples of the whole coal liquid product, distillate fractions of this liquid, and Criterion HDN-60 catalyst were obtained from Southwest Research Inc. Hydrotreating experiments were performed using a continuous operation, unattended, microflow reactor system. A factorial experimental design with three variables (temperature, (310{degrees}C to 388{degrees}C), liquid hourly space velocity (1 to 3 g/h/cm{sup 3}(cat)), pressure (500 to 1000 psig H{sub 2}) is being used in this project. Sulfur and nitrogen contents of the hydrotreated products were monitored during the hydrotreating experiments to ensure that activity was lined out at each set of reaction conditions. Results of hydrotreating the whole coal liquid showed that nitrogen values in the products ranged from 549 ppM at 320{degrees}C, 3 g/h/cm{sup 3}(cat), 500 psig H{sub 2} to <15 ppM at 400{degrees}C, 1 g/h/ cm{sup 3}(cat), 1000 psig H{sub 2}.

Stohl, F.V.; Lott, S.E.; Diegert, K.V.; Goodnow, D.C.; Oelfke, J.B.

1995-06-01T23:59:59.000Z

58

Hydrogen donor solvent coal liquefaction process  

DOE Patents (OSTI)

An indigenous hydrocarbon product stream boiling within a range of from about C.sub.1 -700.degree. F., preferably C.sub.1 -400.degree. F., is treated to produce an upgraded hydrocarbon fuel component and a component which can be recycled, with a suitable donor solvent, to a coal liquefaction zone to catalyze the reaction. In accordance therewith, a liquid hydrocarbon fraction with a high end boiling point range up to about 700.degree. F., preferably up to about 400.degree. F., is separated from a coal liquefaction zone effluent, the separated fraction is contacted with an alkaline medium to provide a hydrocarbon phase and an aqueous extract phase, the aqueous phase is neutralized, and contacted with a peroxygen compound to convert indigenous components of the aqueous phase of said hydrocarbon fraction into catalytic components, such that the aqueous stream is suitable for recycle to the coal liquefaction zone. Naturally occurring phenols and alkyl substituted phenols, found in the aqueous phase, are converted, by the addition of hydroxyl constituents to phenols, to dihydroxy benzenes which, as disclosed in copending Application Ser. Nos. 686,813 now U.S. Pat. No. 4,049,536; 686,814 now U.S. Pat. No. 4,049,537; 686,827 now U.S. Pat. No. 4,051,012 and 686,828, K. W. Plumlee et al, filed May 17, 1976, are suitable hydrogen transfer catalysts.

Plumlee, Karl W. (Baytown, TX)

1978-01-01T23:59:59.000Z

59

A Novel Membrane Reactor for Direct Hydrogen Production from Coal  

DOE Green Energy (OSTI)

Gas Technology Institute is developing a novel concept of membrane gasifier for high efficiency, clean and low cost production of hydrogen from coal. The concept incorporates a hydrogen-selective membrane within a gasification reactor for direct extraction of hydrogen from coal-derived synthesis gases. The objective of this project is to determine the technical and economic feasibility of this concept by screening, testing and identifying potential candidate membranes under high temperature, high pressure, and harsh environments of the coal gasification conditions. The best performing membranes will be selected for preliminary reactor design and cost estimates. To evaluate the performances of the candidate membranes under the gasification conditions, a high temperature/high pressure hydrogen permeation unit has been constructed in this project. The unit is designed to operate at temperatures up to 1100 C and pressures to 60 atm for evaluation of ceramic membranes such as mixed ionic conducting membrane. Several perovskite membranes based on the formulations of BCN (BaCe{sub 0.8}Nd{sub 0.2}O{sub 3-x}) and BCY (BaCe{sub 0.8}Y{sub 0.2}O{sub 3-x}) were prepared by GTI and successfully tested in the new permeation unit. During this reporting period, two different types of membranes, Eu-doped SrCeO{sub 3} (SCE) and SrCe{sub 0.95}Tm{sub 0.05}O{sub 3} (SCTm) provided by the University of Florida and the University of Cincinnati, respectively were tested in the high pressure permeation unit. The SCTm membrane, with a thickness of 1.7 mm, showed the highest hydrogen permeability among the perovskite membranes tested in this project so far. The hydrogen flux measured for the SCTm membrane was close to 0.8 cc/min/cm{sup 2} at a hydrogen feed pressure of about 4 bar at 950 C. SEM and EDX analysis for the tested SCTm membrane showed a separate Ce-rich phase deposited along the grain boundaries in the region towards the feed side of the membrane. No such phase separation was observed towards the permeate side. Partial reduction of the SCTm perovskite material by the high pressure hydrogen, especially in the feed side of the membrane, was postulated to be the possible reason for the phase separation. Further investigation of the stability issue of the perovskite membrane is needed.

Shain Doong, Estela Ong; Mike Atroshenko; Francis Lau; Mike Robers

2004-12-31T23:59:59.000Z

60

NETL: News Release - DOE Advances Production of Hydrogen from Coal  

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

6 , 2006 6 , 2006 DOE Advances Production of Hydrogen from Coal Projects Selected to Address Technological Challenges of Hydrogen Production in Large-Scale Facilities WASHINGTON, DC - The Department of Energy today announced the selection of six research and development projects that will promote the production of hydrogen from coal at large-scale facilities. This central approach will combat climate change by allowing for the capture - and subsequent sequestration - of carbon dioxide generated during hydrogen production. The selections support President Bush's Hydrogen Fuel Initiative, which provides funding for research and technology development to realize a future hydrogen economy that minimizes America's dependence on foreign oil and reduces greenhouse gas emissions.

Note: This page contains sample records for the topic "hydrogen coal derived" 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

A Novel Membrane Reactor for Direct Hydrogen Production From Coal  

DOE Green Energy (OSTI)

Gas Technology Institute has developed a novel concept of a membrane reactor closely coupled with a coal gasifier for direct extraction of hydrogen from coal-derived syngas. The objective of this project is to determine the technical and economic feasibility of this concept by screening, testing and identifying potential candidate membranes under the coal gasification conditions. The best performing membranes were selected for preliminary reactor design and cost estimate. The overall economics of hydrogen production from this new process was assessed and compared with conventional hydrogen production technologies from coal. Several proton-conducting perovskite membranes based on the formulations of BCN (BaCe{sub 0.8}Nd{sub 0.2}O{sub 3-x}), BCY (BaCe{sub 0.8}Y{sub 0.2}O{sub 3-x}), SCE (Eu-doped SrCeO{sub 3}) and SCTm (SrCe{sub 0.95}Tm{sub 0.05}O{sub 3}) were successfully tested in a new permeation unit at temperatures between 800 and 1040 C and pressures from 1 to 12 bars. The experimental data confirm that the hydrogen flux increases with increasing hydrogen partial pressure at the feed side. The highest hydrogen flux measured was 1.0 cc/min/cm{sup 2} (STP) for the SCTm membrane at 3 bars and 1040 C. The chemical stability of the perovskite membranes with respect to CO{sub 2} and H{sub 2}S can be improved by doping with Zr, as demonstrated from the TGA (Thermal Gravimetric Analysis) tests in this project. A conceptual design, using the measured hydrogen flux data and a modeling approach, for a 1000 tons-per-day (TPD) coal gasifier shows that a membrane module can be configured within a fluidized bed gasifier without a substantial increase of the gasifier dimensions. Flowsheet simulations show that the coal to hydrogen process employing the proposed membrane reactor concept can increase the hydrogen production efficiency by more than 50% compared to the conventional process. Preliminary economic analysis also shows a 30% cost reduction for the proposed membrane reactor process, assuming membrane materials meeting DOE's flux and cost target. Although this study shows that a membrane module can be configured within a fluidized bed gasifier, placing the membrane module outside the gasifier in a closely coupled way in terms of temperature and pressure can still offer the same performance advantage. This could also avoid the complicated fluid dynamics and heat transfer issues when the membrane module is installed inside the gasifier. Future work should be focused on improving the permeability and stability for the proton-conducting membranes, testing the membranes with real syngas from a gasifier and scaling up the membrane size.

Shain Doong; Estela Ong; Mike Atrosphenko; Francis Lau; Mike Roberts

2006-01-20T23:59:59.000Z

62

Hydrogenation of coal liquid utilizing a metal carbonyl catalyst  

DOE Patents (OSTI)

Coal liquid having a dissolved transition metal, catalyst as a carbonyl complex such as Co.sub.2 (CO.sub.8) is hydrogenated with hydrogen gas or a hydrogen donor. A dissociating solvent contacts the coal liquid during hydrogenation to form an immiscible liquid mixture at a high carbon monoxide pressure. The dissociating solvent, e.g. ethylene glycol, is of moderate coordinating ability, while sufficiently polar to solvate the transition metal as a complex cation along with a transition metal, carbonyl anion in solution at a decreased carbon monoxide pressure. The carbon monoxide pressure is reduced and the liquids are separated to recover the hydrogenated coal liquid as product. The dissociating solvent with the catalyst in ionized form is recycled to the hydrogenation step at the elevated carbon monoxide pressure for reforming the catalyst complex within fresh coal liquid.

Feder, Harold M. (Hinsdale, IL); Rathke, Jerome W. (Bolingbrook, IL)

1979-01-01T23:59:59.000Z

63

Catalytic two-stage coal hydrogenation process using extinction recycle of heavy liquid fraction  

DOE Patents (OSTI)

A process is described for catalytic two-stage hydrogenation and liquefaction of coal with selective extinction recycle of all heavy liquid fractions boiling above a distillation cut point of about 600--750 F to produce increased yields of low-boiling hydrocarbon liquid and gas products. In the process, the particulate coal feed is slurried with a process-derived liquid solvent normally boiling above about 650 F and fed into a first stage catalytic reaction zone operated at conditions which promote controlled rate liquefaction of the coal, while simultaneously hydrogenating the hydrocarbon recycle oils. The first stage reactor is maintained at 710--800 F temperature, 1,000--4,000 psig hydrogen partial pressure, and 10-90 lb/hr per ft[sup 3] catalyst space velocity. Partially hydrogenated material withdrawn from the first stage reaction zone is passed directly to the second stage catalytic reaction zone maintained at 760--860 F temperature for further hydrogenation and hydroconversion reactions. A 600--750 F[sup +] fraction containing 0--20 W % unreacted coal and ash solids is recycled to the coal slurrying step. If desired, the cut point lower boiling fraction can be further catalytically hydrotreated. By this process, the coal feed is successively catalytically hydrogenated and hydroconverted at selected conditions, to provide significantly increased yields of desirable low-boiling hydrocarbon liquid products and minimal production of hydrocarbon gases, and no net production of undesirable heavy oils and residuum materials. 2 figs.

MacArthur, J.B.; Comolli, A.G.; McLean, J.B.

1989-10-17T23:59:59.000Z

64

Production of jet fuels from coal-derived liquids  

Science Conference Proceedings (OSTI)

Samples of jet fuel (JP-4, JP-8, JP-8X) produced from the liquid by-products of the gasification of lignite coal from the Great Plains Gasification Plant were analyzed to determine the quantity and type of organo-oxygen compounds present. Results were compared to similar fuel samples produced from petroleum. Large quantities of oxygen compounds were found in the coal-derived liquids and were removed in the refining process. Trace quantities of organo-oxygenate compounds were suspected to be present in the refined fuels. Compounds were identified and quantified as part of an effort to determine the effect of these compounds in fuel instability. Results of the analysis showed trace levels of phenols, naphthols, benzofurans, hexanol, and hydrogenated naphthols were present in levels below 100 ppM. 9 figs., 3 tabs.

Knudson, C.L.

1990-06-01T23:59:59.000Z

65

Hydrogen from Bio-Derived Liquids (Presentation)  

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

From Bio-Derived Liquids From Bio-Derived Liquids Hydrogen From Bio Hydrogen From Bio - - Derived Liquids Derived Liquids Dave King, Yong Wang, PNNL BILIWIG Meeting Laurel, Maryland November 6, 2007 Innovation / Overview Innovation / Overview Innovation / Overview Project comprises two components z Ethanol steam reforming z Aqueous phase reforming (APR) Importance to small scale hydrogen production for distributed reforming for hydrogen production ‹ Ethanol is rapidly becoming an infrastructure fuel and is a logical feedstock ‹ APR provides vehicle for facile reforming of a variety of bio-derived feedstocks available in the biorefinery that are not conducive to conventional vapor phase reforming Distinctive technology approach/innovation z We are investigating single step ethanol reforming with emphasis on lower

66

A NOVEL MEMBRANE REACTOR FOR DIRECT HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

Gas Technology Institute is developing a novel concept of membrane gasifier for high efficiency, clean and low cost production of hydrogen from coal. The concept incorporates a hydrogen-selective membrane within a gasification reactor for direct extraction of hydrogen from coal-derived synthesis gases. The objective of this project is to determine the technical and economic feasibility of this concept by screening, testing and identifying potential candidate membranes under high temperature, high pressure, and harsh environments of the coal gasification conditions. The best performing membranes will be selected for preliminary reactor design and cost estimates. To evaluate the performances of the candidate membranes under the gasification conditions, a high temperature/high pressure hydrogen permeation unit has been constructed in this project. The unit is designed to operate at temperatures up to 1100 C and pressures to 60 atm for evaluation of ceramic membranes such as mixed ionic conducting membrane. The unit was fully commissioned and is operational. Several perovskite membranes based on the formulations of BCN (BaCe{sub 0.8}Nd{sub 0.2}O{sub 3-x}) and BCY (BaCe{sub 0.8}Y{sub 0.2}O{sub 3-x}) were prepared by GTI and tested in the new permeation unit. These membranes were fabricated by either uniaxial pressing or tape casting technique with thickness ranging from 0.2 mm to 0.7 mm. Hydrogen permeation data for the BCN perovskite membrane have been successfully obtained for temperatures between 800 and 950 C and pressures from 1 to 12 bar. The highest hydrogen flux was measured at 1.6 STPcc/min/cm{sup 2} at a hydrogen feed pressure of 12 bar and 950 C with a membrane thickness of 0.22 mm. A membrane gasification reactor model was developed to consider the H{sub 2} permeability of the membrane, the kinetics and the equilibriums of the gas phase reactions in the gasifier, the operating conditions and the configurations of the membrane reactor. The results show that the hydrogen production efficiency using the novel membrane gasification reactor concept can be increased by about 50% versus the conventional gasification process. This confirms the previous evaluation results from the thermodynamic equilibrium calculation. A rigorous model for hydrogen permeation through mixed proton-electron conducting ceramic membranes was also developed based on non-equilibrium thermodynamics. The hydrogen flux predicted from the modeling results are in line with the data from the experimental measurement. The simulation also shows that the presence of steam in the permeate side or the feed side of the membrane can have a small negative effect on the hydrogen flux, in the order of 10%.

Shain Doong; Estela Ong; Mike Atroshenko; Francis Lau; Mike Roberts

2004-10-26T23:59:59.000Z

67

High Hydrogen, Low Methane Syngas from Low-Rank Coals for Coal-to-Liquids  

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

High Hydrogen, Low Methane Syngas from Low-Rank Coals for Coal-to-Liquids Production High Hydrogen, Low Methane Syngas from Low-Rank Coals for Coal-to-Liquids Production Southern Research Institute (SRI) Project Number: FE0012054 Project Description The focus of the project will be to develop, test, and optimize steam-reforming catalysts for converting tars, C2+ hydrocarbons, NH3, and CH4 in high-temperature and sulfur environments, increasing the ratio of hydrogen in syngas, as part of a modified, advanced gasification platform for the conversion of low-rank coals to syngas for coal-to-liquid and integrated gasification combined cycle applications. Project Details Program Background and Project Benefits Project Scope and Technology Readiness Level Accomplishments Contacts, Duration, and Cost Project Images Abstract Performer website: Southern Research Institute

68

Alcohols as hydrogen-donor solvents for treatment of coal  

DOE Patents (OSTI)

A method for the hydroconversion of coal by solvent treatment at elevated temperatures and pressure wherein an alcohol having an .alpha.-hydrogen atom, particularly a secondary alcohol such as isopropanol, is utilized as a hydrogen donor solvent. In a particular embodiment, a base capable of providing a catalytically effective amount of the corresponding alcoholate anion under the solvent treatment conditions is added to catalyze the alcohol-coal reaction.

Ross, David S. (Palo Alto, CA); Blessing, James E. (Menlo Park, CA)

1981-01-01T23:59:59.000Z

69

A NOVEL MEMBRANE REACTOR FOR DIRECT HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

Gas Technology Institute is developing a novel concept of membrane reactor coupled with a gasifier for high efficiency, clean and low cost production of hydrogen from coal. The concept incorporates a hydrogen-selective membrane within a gasification reactor for direct extraction of hydrogen from coal-derived synthesis gases. The objective of this project is to determine the technical and economic feasibility of this concept by screening, testing and identifying potential candidate membranes under high temperature, high pressure, and harsh environments of the coal gasification conditions. The best performing membranes will be selected for preliminary reactor design and cost estimates. To evaluate the performances of the candidate membranes under the gasification conditions, a high temperature/high pressure hydrogen permeation unit has been constructed in this project. The unit is designed to operate at temperatures up to 1100 C and pressures to 60 atm for evaluation of ceramic membranes such as mixed protonic-electronic conducting membrane. Several perovskite membranes based on the formulations of BCN (BaCe{sub 0.8}Nd{sub 0.2}O{sub 3-x}), BCY (BaCe{sub 0.8}Y{sub 0.2}O{sub 3-x}), Eu-doped SrCeO{sub 3} (SCE) and SrCe{sub 0.95}Tm{sub 0.05}O{sub 3} (SCTm) were successfully tested in the new permeation unit. During this reporting period, a thin BCN membrane supported on a porous BCN layer was fabricated. The objective was to increase the hydrogen flux with a further reduction of the thickness of the active membrane layer. The thinnest dense layer that could be achieved in our laboratory currently was about 0.2 mm. Nevertheless, the membrane was tested in the permeation unit and showed reasonable flux compared to the previous BCN samples of the same thickness. A long term durability test was conducted for a SCTm membrane with pure hydrogen in the feed side and nitrogen in the sweep side. The pressure was 1 bar and the temperature was around 1010 C. No decline of hydrogen flux was observed after continuous running of over 250 hours. This long term test indicates that the perovskite membrane has good thermal stability under the reducing conditions of the hydrogen atmosphere. A conceptual design of the membrane reactor configuration for a 1000 tons-per-day (TPD) coal gasifier was completed. The design considered a tubular membrane module located within the freeboard area of a fluidized bed gasifier. The membrane ambipolar conductivity was based on the value calculated from the measured permeation data. A membrane thickness of 25 micron was assumed in the calculation. The GTI's gasification model combined with a membrane reactor model were used to determine the dimensions of the membrane module. It appears that a membrane module can be configured within a fluidized bed gasifier without substantial increase of the gasifier dimensions.

Shain Doong; Estela Ong; Mike Atroshenko; Francis Lau; Mike Roberts

2005-04-28T23:59:59.000Z

70

NETL: Coal & Coal Biomass to Liquids - Hydrogen and Clean Fuels...  

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

by reacting steam with natural gas at high temperatures, a process called steam methane reforming (SMR). Pressurized hydrogen storage tank by Quantum Hydrogen has a high...

71

Integrated Warm Gas Multicontaminant Cleanup Technologies for Coal-Derived Syngas  

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

Integrated Warm Gas Multicontaminant Integrated Warm Gas Multicontaminant Cleanup Technologies for Coal-Derived Syngas Description Integrated Gasification Combined Cycle (IGCC) technology offers a means to utilize coal -the most abundant fuel in the United States-to produce a host of products, ranging from electricity to value-added chemicals like transportation fuels and hydrogen, in an efficient, environmentally friendly manner. However, the overall cost (capital, operating,

72

NETL: Coal & Coal Biomass to Liquids - Alternate Hydrogen Production  

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

Deepwater Technology Enhanced Oil Recovery Gas Hydrates Natural Gas Resources Contacts Coal & Power Systems Major Demonstrations Innovations for Existing Plants Gasification...

73

NETL: Coal & Coal Biomass to Liquids - Hydrogen and Clean Fuels...  

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

Deepwater Technology Enhanced Oil Recovery Gas Hydrates Natural Gas Resources Contacts Coal & Power Systems Major Demonstrations Innovations for Existing Plants Gasification...

74

Hydrogen separation by ceramic membranes in coal gasification  

DOE Green Energy (OSTI)

Project objectives are to develop hydrogen-permselective ceramic membranes for water-gas shift membrane-reactor suitable for hydrogen production from coal gas, and to evaluate the technical and economic potential of the membrane-reactor. Work performed during reporting period included membrane deposition and stability testing.

Gavalas, G.R.

1992-07-08T23:59:59.000Z

75

Hydrogen production with coal using a pulverization device  

DOE Patents (OSTI)

The present invention relates generally to the production of gaseous hydrogen with carbonous materials in the presence of steam by the steam-carbon reaction, and more particularly to such generation of hydrogen by rapidly comminuting coal in the presence of high-temperature steam.

Paulson, L.E.

1986-12-12T23:59:59.000Z

76

Long-Term Demonstration of Hydrogen Production from Coal at Elevated Temperatures Year 6 - Activity 1.12 - Development of a National Center for Hydrogen Technology  

Science Conference Proceedings (OSTI)

The Energy & Environmental Research Center (EERC) has continued the work of the National Center for Hydrogen Technology (NCHT) Program Year 6 Task 1.12 project to expose hydrogen separation membranes to coal-derived syngas. In this follow-on project, the EERC has exposed two membranes to coal-derived syngas produced in the pilot-scale transport reactor development unit (TRDU). Western Research Institute (WRI), with funding from the State of Wyoming Clean Coal Technology Program and the North Dakota Industrial Commission, contracted with the EERC to conduct testing of WRIs coal-upgrading/gasification technology for subbituminous and lignite coals in the EERCs TRDU. This gasifier fires nominally 200500 lb/hour of fuel and is the pilot-scale version of the full-scale gasifier currently being constructed in Kemper County, Mississippi. A slipstream of the syngas was used to demonstrate warm-gas cleanup and hydrogen separation using membrane technology. Two membranes were exposed to coal-derived syngas, and the impact of coal-derived impurities was evaluated. This report summarizes the performance of WRIs patent-pending coalupgrading/ gasification technology in the EERCs TRDU and presents the results of the warm-gas cleanup and hydrogen separation tests. Overall, the WRI coal-upgrading/gasification technology was shown to produce a syngas significantly lower in CO2 content and significantly higher in CO content than syngas produced from the raw fuels. Warm-gas cleanup technologies were shown to be capable of reducing sulfur in the syngas to 1 ppm. Each of the membranes tested was able to produce at least 2 lb/day of hydrogen from coal-derived syngas.

Stanislowski, Joshua; Tolbert, Scott; Curran, Tyler; Swanson, Michael

2012-04-30T23:59:59.000Z

77

Prediction of thermodynamic properties of coal derivatives  

Science Conference Proceedings (OSTI)

The purpose of this research program is to understand the relationship between macroscopic thermodynamic properties and the various types of intermolecular forces. Since coal-derived liquids contain a wide variety of compounds, a theory capable of successfully predicting the thermophysical properties for coal processes must take into account the molecular shapes and all significant intermolecular forces: dispersion forces, anisotropic forces due to dipoles and quadrupoles, as well as Lewis acid-base interactions. We have developed the Acid-Base-Perturbed-Anisotropic-Chain Theory (ABPACT), a comprehensive theory that is capable of predicting the thermophysical properties for many systems where these different intermolecular forces are present. The ABPACT can treat non-polar compounds, polar compounds and compounds that associate through Lewis acid-base interactions. In addition to our theoretical work, we have used computer simulations to evaluate (and in some cases correct) the assumptions made in this theory. We also have conducted experiments to help us better understand the interplay of different kinds of interactions in multicomponent mixtures.

Donohue, M.D.

1990-09-01T23:59:59.000Z

78

NOVEL SLURRY PHASE DIESEL CATALYSTS FOR COAL-DERIVED SYNGAS  

DOE Green Energy (OSTI)

This report describes research conducted to support the DOE program in novel slurry phase catalysts for converting coal-derived synthesis gas to diesel fuels. The primary objective of this research program is to develop attrition resistant catalysts that exhibit high activities for conversion of coal-derived syngas.

Dr. Dragomir B. Bukur; Dr. Ketil Hanssen; Alec Klinghoffer; Dr. Lech Nowicki; Patricia O'Dowd; Dr. Hien Pham; Jian Xu

2001-01-07T23:59:59.000Z

79

Separating hydrogen from coal gasification gases with alumina membranes  

DOE Green Energy (OSTI)

Synthesis gas produced in coal gasification processes contains hydrogen, along with carbon monoxide, carbon dioxide, hydrogen sulfide, water, nitrogen, and other gases, depending on the particular gasification process. Development of membrane technology to separate the hydrogen from the raw gas at the high operating temperatures and pressures near exit gas conditions would improve the efficiency of the process. Tubular porous alumina membranes with mean pore radii ranging from about 9 to 22 {Angstrom} have been fabricated and characterized. Based on hydrostatic tests, the burst strength of the membranes ranged from 800 to 1600 psig, with a mean value of about 1300 psig. These membranes were evaluated for separating hydrogen and other gases. Tests of membrane permeabilities were made with helium, nitrogen, and carbon dioxide. Measurements were made at room temperature in the pressure range of 15 to 589 psi. Selected membranes were tested further with mixed gases simulating a coal gasification product gas. 5 refs., 7 figs.

Egan, B.Z. (Oak Ridge National Lab., TN (USA)); Fain, D.E.; Roettger, G.E.; White, D.E. (Oak Ridge K-25 Site, TN (USA))

1991-01-01T23:59:59.000Z

80

NETL: Coal & Coal Biomass to Liquids - Hydrogen and Clean Fuels...  

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

force). The illustration at right is an artists conception of a hydrogen atom; quantum physics shows that the electron does not appear in one place, but behaves as a...

Note: This page contains sample records for the topic "hydrogen coal derived" 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

A NOVEL MEMBRANE REACTOR FOR DIRECT HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

Gas Technology Institute is developing a novel concept of membrane gasifier for high efficiency, clean and low cost production of hydrogen from coal. The concept incorporates a hydrogen-selective membrane within a gasification reactor for direct extraction of hydrogen from coal synthesis gases. The objective of this project is to determine the technical and economic feasibility of this concept by screening, testing and identifying the potential candidate membranes under high temperature, high pressure, and harsh environments of the coal gasification conditions. The best performing membranes will be selected for preliminary reactor design and cost estimates. To evaluate the candidate membrane performance under the gasification conditions, a high temperature/high pressure hydrogen permeation unit will be constructed in this project. During this reporting period, the design of this unit was completed. The unit will be capable of operating at temperatures up to 1100 C and pressures to 60 atm for evaluation of ceramic membranes such as mixed ionic conducting membrane. The membranes to be tested will be in disc form with a diameter of about 3 cm. By operating at higher temperatures and higher hydrogen partial pressures, we expect to demonstrate commercially relevant hydrogen flux, 10 {approx} 50 cc/min/cm{sup 2}, from the membranes made of the perovskite type of ceramic material. The construction of the unit is planned to be completed by the end of the next reporting period.

Shain Doong; Estela Ong; Mike Atroshenko; Francis Lau; Mike Roberts

2004-01-22T23:59:59.000Z

82

Hydrogen Resource Assessment: Hydrogen Potential from Coal, Natural Gas, Nuclear, and Hydro Power  

DOE Green Energy (OSTI)

This paper estimates the quantity of hydrogen that could be produced from coal, natural gas, nuclear, and hydro power by county in the United States. The study estimates that more than 72 million tonnes of hydrogen can be produced from coal, natural gas, nuclear, and hydro power per year in the country (considering only 30% of their total annual production). The United States consumed about 396 million tonnes of gasoline in 2007; therefore, the report suggests the amount of hydrogen from these sources could displace about 80% of this consumption.

Milbrandt, A.; Mann, M.

2009-02-01T23:59:59.000Z

83

Process for removal of mineral particulates from coal-derived liquids  

SciTech Connect

Suspended mineral solids are separated from a coal-derived liquid containing the solids by a process comprising the steps of: (a) contacting said coal-derived liquid containing solids with a molten additive having a melting point of 100.degree.-500.degree. C. in an amount of up to 50 wt. % with respect to said coal-derived liquid containing solids, said solids present in an amount effective to increase the particle size of said mineral solids and comprising material or mixtures of material selected from the group of alkali metal hydroxides and inorganic salts having antimony, tin, lithium, sodium, potassium, magnesium, calcium, beryllium, aluminum, zinc, molybdenum, cobalt, nickel, ruthenium, rhodium or iron cations and chloride, iodide, bromide, sulfate, phosphate, borate, carbonate, sulfite, or silicate anions; and (b) maintaining said coal-derived liquid in contact with said molten additive for sufficient time to permit said mineral matter to agglomerate, thereby increasing the mean particle size of said mineral solids; and (c) recovering a coal-derived liquid product having reduced mineral solids content. The process can be carried out with less than 5 wt. % additive and in the absence of hydrogen pressure.

McDowell, William J. (Knoxville, TN)

1980-01-01T23:59:59.000Z

84

CAPITAL AND OPERATING COST OF HYDROGEN PRODUCTION FROM COAL GASIFICATION  

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

CAPITAL AND OPERATING COST OF HYDROGEN CAPITAL AND OPERATING COST OF HYDROGEN PRODUCTION FROM COAL GASIFICATION Final Report April 2003 Prepared for: The United States Department of Energy National Energy Technology Laboratory (NETL) under: Contract No. DE-AM26-99FT40465 between the NETL and Concurrent Technologies Corporation (CTC) Subcontract No. 990700362 between CTC and Parsons Infrastructure & Technology Group Inc. Task 50611 DOE Task Managers: James R. Longanbach Gary J. Stiegel Parsons Project Manager: Michael D. Rutkowski Principal Investigators: Thomas L. Buchanan Michael G. Klett Ronald L. Schoff PARSONS Capital and Operating Cost of Hydrogen Production from Coal Gasification Page i April 2003 TABLE OF CONTENTS Section Title Page List of Tables iii List of Figures iii

85

Short residence time coal liquefaction process including catalytic hydrogenation  

DOE Patents (OSTI)

Normally solid dissolved coal product and a distillate liquid product are produced by continuously passing a feed slurry comprising raw feed coal and a recycle solvent oil and/or slurry together with hydrogen to a preheating-reaction zone, the hydrogen pressure in the preheating-reaction zone being at least 1,500 psig (105 kg/cm[sup 2]), reacting the slurry in the preheating-reaction zone at a temperature in the range of between about 455 and about 500 C to dissolve the coal to form normally liquid coal and normally solid dissolved coal. A total slurry residence time is maintained in the reaction zone ranging from a finite value from about 0 to about 0.2 hour, and reaction effluent is continuously and directly contacted with a quenching fluid to substantially immediately reduce the temperature of the reaction effluent to below 425 C to substantially inhibit polymerization so that the yield of insoluble organic matter comprises less than 9 weight percent of said feed coal on a moisture-free basis. The reaction is performed under conditions of temperature, hydrogen pressure and residence time such that the quantity of distillate liquid boiling within the range C[sub 5]-454 C is an amount at least equal to that obtainable by performing the process under the same condition except for a longer total slurry residence time, e.g., 0.3 hour. Solvent boiling range liquid is separated from the reaction effluent and recycled as process solvent. The amount of solvent boiling range liquid is sufficient to provide at least 80 weight percent of that required to maintain the process in overall solvent balance. 6 figs.

Anderson, R.P.; Schmalzer, D.K.; Wright, C.H.

1982-05-18T23:59:59.000Z

86

Short residence time coal liquefaction process including catalytic hydrogenation  

DOE Patents (OSTI)

Normally solid dissolved coal product and a distillate liquid product are produced by continuously passing a feed slurry comprising raw feed coal and a recycle solvent oil and/or slurry together with hydrogen to a preheating-reaction zone (26, alone, or 26 together with 42), the hydrogen pressure in the preheating-reaction zone being at least 1500 psig (105 kg/cm.sup.2), reacting the slurry in the preheating-reaction zone (26, or 26 with 42) at a temperature in the range of between about 455.degree. and about 500.degree. C. to dissolve the coal to form normally liquid coal and normally solid dissolved coal. A total slurry residence time is maintained in the reaction zone ranging from a finite value from about 0 to about 0.2 hour, and reaction effluent is continuously and directly contacted with a quenching fluid (40, 68) to substantially immediately reduce the temperature of the reaction effluent to below 425.degree. C. to substantially inhibit polymerization so that the yield of insoluble organic matter comprises less than 9 weight percent of said feed coal on a moisture-free basis. The reaction is performed under conditions of temperature, hydrogen pressure and residence time such that the quantity of distillate liquid boiling within the range C.sub.5 -454.degree. C. is an amount at least equal to that obtainable by performing the process under the same condition except for a longer total slurry residence time, e.g., 0.3 hour. Solvent boiling range liquid is separated from the reaction effluent (83) and recycled as process solvent (16). The amount of solvent boiling range liquid is sufficient to provide at least 80 weight percent of that required to maintain the process in overall solvent balance.

Anderson, Raymond P. (Overland Park, KS); Schmalzer, David K. (Englewood, CO); Wright, Charles H. (Overland Park, KS)

1982-05-18T23:59:59.000Z

87

Small-scale costs of hydrogen derived from ammonia. [As ammonia  

SciTech Connect

A systems study was made to assess the economic prospects for using purchased industrial ammonia as a hydrogen distribution and storage medium for users requiring 33 to 330 million std ft/sup 3/ per year (MSCFY) of hydrogen (or 0.1 to 1.0 MSCFD) at a plant capacity factor of 0.9. Projected costs to the end user were determined for the dissociated ammonia product (75 vol % hydrogen, 25 vol % nitrogen), and for ultra-high-purity hydrogen (99.999%) obtained by separation of the nitrogen. Costs were also projected for hydrogen produced by steam-reforming of natural gas, for electrolytic hydrogen, and for purchased (merchant) liquid hydrogen. The costs of ammonia and its hydrogen, and liquid hydrogen made by ocean thermal energy conversion (OTEC), are also listed for comparison. The latter costs from a recent study were updated to include more realistic (higher) hydrogen purification costs. All of the costs, expressed as 1980 $/MBTU in 1990, were obtained for two sets of forecast energy prices on the basis that advanced technology electrolyzers and OTEC products would be available in 1990. Results of the analysis showed that merchant liquid hydrogen was substantially higher in cost than all of the other options. Although hydrogen derived from industrial ammonia was significantly higher in cost than electrolytic hydrogen or hydrogen derived from OTEC ammonia, it can be produced using state-of-the-art technology. Possible reductions in the total cost of obtaining hydrogen via ammonia could make it lower in cost than electrolytic hydrogen. Hydrogen produced from natural gas was lowest in cost, among the land-based sources, for plant sizes exceeding 100 MSCFY. Other comparisons are provided, including the cost of ammonia made from coal. The criteria and methodology applied in the study are described. Uses of the product hydrogen are suggested along with recommendations for future work.

Strickland, G.

1981-10-01T23:59:59.000Z

88

Alternative Fuels Data Center: Hydrogenation-Derived Renewable Diesel  

Alternative Fuels and Advanced Vehicles Data Center (EERE)

Emerging Fuels Emerging Fuels Printable Version Share this resource Send a link to Alternative Fuels Data Center: Hydrogenation-Derived Renewable Diesel to someone by E-mail Share Alternative Fuels Data Center: Hydrogenation-Derived Renewable Diesel on Facebook Tweet about Alternative Fuels Data Center: Hydrogenation-Derived Renewable Diesel on Twitter Bookmark Alternative Fuels Data Center: Hydrogenation-Derived Renewable Diesel on Google Bookmark Alternative Fuels Data Center: Hydrogenation-Derived Renewable Diesel on Delicious Rank Alternative Fuels Data Center: Hydrogenation-Derived Renewable Diesel on Digg Find More places to share Alternative Fuels Data Center: Hydrogenation-Derived Renewable Diesel on AddThis.com... More in this section... Biobutanol Drop-In Biofuels Methanol

89

Bio-Derived Liquids to Hydrogen Distributed Reforming Targets (Presentation)  

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

Distributed Reforming Targets Arlene F. Anderson Technology Development Manager, U.S. DOE Office of Energy Efficiency and Renewable Energy Hydrogen, Fuel Cells and Infrastructure Technologies Program Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group and Hydrogen Production Technical Team Review November 6, 2007 Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group (BILIWG) The Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group (BILIWG), launched in October 2006, provides a forum for effective communication and collaboration among participants in DOE Hydrogen, Fuel Cells, and Infrastructure Technologies Program (HFCIT) cost-shared research directed at distributed bio-liquid reforming. The Working Group includes

90

A NOVEL MEMBRANE REACTOR FOR DIRECT HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

Gas Technology Institute is developing a novel concept of membrane gasifier for high efficiency, clean and low cost production of hydrogen from coal. The concept incorporates a hydrogen-selective membrane within a gasification reactor for direct extraction of hydrogen from coal synthesis gases. The objective of this project is to determine the technical and economic feasibility of this concept by screening, testing and identifying potential candidate membranes under high temperature, high pressure, and harsh environments of the coal gasification conditions. The best performing membranes will be selected for preliminary reactor design and cost estimates. To evaluate the performances of the candidate membranes under the gasification conditions, a high temperature/high pressure hydrogen permeation unit will be constructed in this project. During this reporting period, the mechanical construction of the permeation unit was completed. Commissioning and shake down tests are being conducted. The unit is capable of operation at temperatures up to 1100 C and pressures to 60 atm for evaluation of ceramic membranes such as mixed ionic conducting membrane. The membranes to be tested will be in disc form with a diameter of about 3 cm. Operation at these high temperatures and high hydrogen partial pressures will demonstrate commercially relevant hydrogen flux, 10{approx}50 cc/min/cm{sup 2}, from the membranes made of the perovskite type of ceramic material. Preliminary modeling was also performed for a tubular membrane reactor within a gasifier to estimate the required membrane area for a given gasification condition. The modeling results will be used to support the conceptual design of the membrane reactor.

Shain Doong; Estela Ong; Mike Atroshenko; Mike Roberts; Francis Lau

2004-04-26T23:59:59.000Z

91

CERAMIC MEMBRANES FOR HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

The objective of this project is to develop ceramic membranes for hydrogen separation from fuel gas or synthesis gas at temperatures 400-500 C. The membrane chosen for this purpose consists of a dense silica layer coated on a porous support by chemical vapor depositrion (CVD). The support used during the reporting period was zeolite silicalite grown on macroporous alumina tubes. Chemical vapor deposition was carried out using alternating exposure of the support to silicon tetrachloride (SiCl{sub 4}) and water vapor at 400-500 C. Under these conditions it takes about twenty-five reaction cycles to narrow down the pores of the zeolite support sufficiently for separation of hydrogen from other gases. The membranes were characterized by gas adsorption for pore size distribution, scanning electron microscopy, and EDAX for elemental composition. The permeance of H{sub 2}, N{sub 2}, CO{sub 2}, n-C{sub 4}H{sub 10}, and i-C{sub 4}H{sub 10} was measured in the temperature range 100-250 C. At 150 C, the H{sub 2}:N{sub 2} permeance ratio was in the range 100-200 at a hydrogen permeance of 5-10x10{sup -8} mol/m{sub 2}-s-Pa.

George R. Gavalas

2003-03-18T23:59:59.000Z

92

A fresh look at coal-derived liquid fuels  

Science Conference Proceedings (OSTI)

35% of the world's energy comes from oil, and 96% of that oil is used for transportation. The current number of vehicles globally is estimated to be 700 million; that number is expected to double overall by 2030, and to triple in developing countries. Now consider that the US has 27% of the world's supply of coal yet only 2% of the oil. Coal-to-liquids technologies could bridge the gap between US fuel supply and demand. The advantages of coal-derived liquid fuels are discussed in this article compared to the challenges of alternative feedstocks of oil sands, oil shale and renewable sources. It is argued that pollutant emissions from coal-to-liquid facilities could be minimal because sulfur compounds will be removed, contaminants need to be removed for the FT process, and technologies are available for removing solid wastes and nitrogen oxides. If CO{sub 2} emissions for coal-derived liquid plants are captured and sequestered, overall emissions of CO{sub 2} would be equal or less than those from petroleum. Although coal liquefaction requires large volumes of water, most water used can be recycled. Converting coal to liquid fuels could, at least in the near term, bring a higher level of stability to world oil prices and the global economy and could serve as insurance for the US against price hikes from oil-producing countries. 7 figs.

Paul, A.D. [Benham Companies LLC (USA)

2009-01-15T23:59:59.000Z

93

Novel hydrogen separation device development for coal gasification system applications. Final report  

DOE Green Energy (OSTI)

This study was undertaken for the development of a novel Electrochemical Hydrogen Separator (EHS) technology for low-cost hydrogen separation from coal derived gases. Design and operating parameter testing was performed using subscale cells (25 cm{sup 2}). High H{sub 2} purity, >99% is one of the main features of the EHS. It was found that N{sub 2}, CO{sub 2} and CH{sub 4} behave as equivalent inerts; EHS performance is not affected by the balance of feed gas containing these components. This product purity level is not sacrificed by increased H{sub 2} recovery. CO, however, does adversely affect EHS performance and therefore feed stream pretreatment is recommended. Low levels of H{sub 2}S and NH{sub 3} were added to the feed gas stream and it was verified that these impurities did not affect EHS performance. Task 2 demonstrated the scale-up to full size multi-cell module operation while maintaining a stable energy requirement. A 10-cell full-size module (1050 cm{sup 2} cell active area) was operated for over 3,800 hours and gave a stable baseline performance. Several applications for the EHS were investigated. The most economically attractive systems incorporating an EHS contain low pressure, dilute hydrogen streams, such as coal gasification carbonate fuel cell systems, hydrogen plant purification and fluid catalytic cracker units. In addition, secondary hydrogen recovery from PSA or membrane tailstreams using an EHS may increase overall system efficiency.

Not Available

1993-08-01T23:59:59.000Z

94

Combustion rates and mechanisms of pulverized coals and coal-derived fuels  

SciTech Connect

Increased use of coal, our most abundant fossil fuel resource, will be required to meet both immediate and long-term energy demands. Improvement in existing technologies of steam raising and industrial process heating through the clean, direct firing of pulverized coal will have major and immediate impact. Improvements are required because of the unacceptably high emissions from present coal combustion systems and because of the need to couple considerations of pollutant emissions and carbon conversion efficiencies. The rates and mechanisms of coal devolatilization and combustion are extremely sensitive to local details of the combustion process. Similarly, pollutants formed during the process are sensitive to the initial coal composition and local time and temperature histories of individual particles. Very little useful information is available by which the influence of combustion modifications on both the efficiency and pollutant emission characteristics can be predicted. The present understanding of the rates of coal and char combustion is summarized with the conclusion that heterogeneous chemical kinetic rates strongly influence the rates and mechanisms of coal and char combustion. If understood, adjustment and control of the rates and mechanisms by judicious adjustment of the combustion process and the initial fuel character should be possible. A proposal for a detailed theoretical and experimental study of the combustion rates of pulverized coal and coal-derived fuels is discussed.

Hardesty, D.R.

1976-06-01T23:59:59.000Z

95

Production of hydrogen and coproducts from coal  

DOE Green Energy (OSTI)

Between the TGA and CPU data, a number of general conclusions have been developed, regarding both selection of catalysts and selection of the most effective and economic approaches to scaled-up process development. (Hauserman, 1992) These conclusions are in an order that is not meant to imply relative importance. (1) Impregnation of Wyodak coal with KOH, at a potassium-to-fixed carbon ratio of around 0.2 or greater, roughly doubles the gasification reaction rate in fluidized beds of limestone. Soluble potassium, in any convenient form, is recommended as a rate-enhancing catalyst, subject to supply costs and efficiency of recovery by leaching. (2) In a fluidized bed of taconite, the reaction rate enhancement by potassium impregnation appears at least as great as in a limestone bed. (3) Reactivity coefficients defined by continuous test results are a different but closely related property and are substantially lower than standard TGA-determined reactivities. (4) The most useful result from the CPU is determination of specific capacities, defined as pounds per hour of fixed carbon converted per volume of reaction vessel. (5) Potassium impregnation clearly enhances reaction rates, but in a practical process will require an efficient leaching step for potassium recovery to be economically viable. (6) Earlier TGA results suggest that a weight ratio of potassium to fixed carbon (FC) of roughly 0.4 will give maximum reactivity enhancement. (7) For these CPU tests, control over the actual degree of potassium impregnation during feed impregnation proved more difficult than expected, apparently leaving a lot of the KOH catalyst free (non-ion exchanged) and subject to segregation during handling and feeding, as well as in the gasifier itself.

Hauserman, W.B.

1992-11-01T23:59:59.000Z

96

Production of hydrogen and coproducts from coal  

DOE Green Energy (OSTI)

Between the TGA and CPU data, a number of general conclusions have been developed, regarding both selection of catalysts and selection of the most effective and economic approaches to scaled-up process development. (Hauserman, 1992) These conclusions are in an order that is not meant to imply relative importance. (1) Impregnation of Wyodak coal with KOH, at a potassium-to-fixed carbon ratio of around 0.2 or greater, roughly doubles the gasification reaction rate in fluidized beds of limestone. Soluble potassium, in any convenient form, is recommended as a rate-enhancing catalyst, subject to supply costs and efficiency of recovery by leaching. (2) In a fluidized bed of taconite, the reaction rate enhancement by potassium impregnation appears at least as great as in a limestone bed. (3) Reactivity coefficients defined by continuous test results are a different but closely related property and are substantially lower than standard TGA-determined reactivities. (4) The most useful result from the CPU is determination of specific capacities, defined as pounds per hour of fixed carbon converted per volume of reaction vessel. (5) Potassium impregnation clearly enhances reaction rates, but in a practical process will require an efficient leaching step for potassium recovery to be economically viable. (6) Earlier TGA results suggest that a weight ratio of potassium to fixed carbon (FC) of roughly 0.4 will give maximum reactivity enhancement. (7) For these CPU tests, control over the actual degree of potassium impregnation during feed impregnation proved more difficult than expected, apparently leaving a lot of the KOH catalyst free (non-ion exchanged) and subject to segregation during handling and feeding, as well as in the gasifier itself.

Hauserman, W.B.

1992-01-01T23:59:59.000Z

97

Hydrogen separation by ceramic membranes in coal gasification  

DOE Green Energy (OSTI)

Project Objectives are to develop hydrogen-permselective ceramic membranes for water-gas shift membrane-reactor suitable for hydrogen production from coal gas and evaluate the technical and economic potential of the membrane-reactor. During the reporting period exploratory experiments begun on a membrane preparation technique aimed at providing higher membrane permeance. The new preparation technique involves two stages. The first stage is the formation of a layer of silica gel by a two-phase interfacial reaction within the pores of the substrate. The gel is then dried and calcined yielding a microporous (pore diameter below 10 [Angstrom]) silica layer within the pores of the substrate tube. The second stage involves one-sided chemical vapor deposition using the SiCl[sub 4]-H[sub 2]O reaction to close up the micropores of the gel layer and produce the final hydrogen permselective membrane. Chemical reactions involved are described.

Gavalas, G.R.

1992-04-30T23:59:59.000Z

98

CERAMIC MEMBRANES FOR HYDROGEN PRODUCTION FROM COAL  

DOE Green Energy (OSTI)

The present project is devoted to developing hydrogen permselective silica membranes supported on composite supports to achieve high flux and selectivity. The supports consist of a thin zeolite silicalite layer coated on {alpha}-Al{sub 2}O{sub 3} tubes of mean pore size 1 {micro}m. The zeolite layer is grown by reaction in a suitable silicate solution at 95 C. After two or three reaction periods a layer of silicalite crystals about 20 {micro}m thick grows inside the pores of alumina. In addition to the zeolitic pores, this layer contains voids of a few nanometer diameter that remain between the crystals or between the crystals and the pore walls. The quality of the silicalite/alumina composites was evaluated by gas permeation measurements and by nitrogen adsorption and it was found that the residual voids were below 5 nm in diameter. Three techniques were investigated for chemical vapor deposition (CVD) of the silica layer on the silicalite/alumina composite support. The first was TEOS pyrolysis at approximately one millibar partial pressure and 650 C. After 8 h reaction the fluxes of hydrogen and nitrogen at ambient temperature had declined by a factor of approximately 100 indicating sealing of defects and zeolitic pores alike. The second CVD technique investigated was SiCl{sub 4} hydrolysis at 90 C. Deposition in this case was conducted in a series of cycles, each cycle comprising two half reactions, i.e. exposure to SiCl{sub 4} followed by exposure to water vapor. The deposition was interrupted every five cycles to measure the permeation properties of the nascent membrane at 120 C. After a few cycles the membrane pores were sealed, but the silica layer was not thermally stable when the temperature was raised to 400 C. In the third technique investigated, silica deposition was carried out by SiCl{sub 4} hydrolysis at 400 C, again in a sequence of half reaction cycles. After 15 cycles the membrane pores were well sealed by a layer stable to at least 400 C.

George R. Gavalas

2001-11-27T23:59:59.000Z

99

Fuel Cell Technologies Office: Bio-Derived Liquids to Hydrogen...  

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

Meeting - November 2007 to someone by E-mail Share Fuel Cell Technologies Office: Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group Meeting - November 2007 on...

100

Co-Production of Pure Hydrogen and Electricity from Coal Syngas ...  

Science Conference Proceedings (OSTI)

Presentation Title, Co-Production of Pure Hydrogen and Electricity from Coal Syngas via the Steam-Iron Process Using Promoted Iron-Based Catalysts Sub-

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101

Prediction of thermodynamic properties of coal derivatives  

Science Conference Proceedings (OSTI)

The purpose of this research program is to understand and model the effect of the different intermolecular forces on the thermodynamic properties of systems containing pure compounds and mixtures. The compounds under consideration vary considerably in size, shape and energy. Therefore in order to develop a theory capable of describing accurately the thermodynamic properties and phase behavior of such systems over a wide range of temperature and pressure, one has to take into account explicitly the differences in shape and size among the various compounds as well as the different type of intermolecular interactions. In order to get a better understanding of the intermolecular forces and to test some of our recent models, we have performed considerable experimental work. We used FTIR to examine hydrogen bonding interactions between small molecules and between small molecules and polymers. In addition, we investigated experimentally the high pressure phase behavior of ternary and quaternary systems exhibiting polar and hydrogen bonding interactions.

Donohue, M.D.

1991-10-01T23:59:59.000Z

102

Biomass-Derived Hydrogen from a Thermally Ballasted Gasifier  

E-Print Network (OSTI)

Biomass-Derived Hydrogen from a Thermally Ballasted Gasifier DOE Hydrogen Program Contractors biomass #12;Approach Outline Gasifier Pilot Plant· Develop subsystems for the hydrogen production system heated gasifier Q Air N2 H2O CO2 O2 Steam H2 CO CO2 CmHn Biomass 45 kg/hr Biomass 180 kg/hr Sand Bed: 43

103

COAL/POLYMER COPROCESSING WITH EFFICIENT USE OF HYDROGEN  

DOE Green Energy (OSTI)

Inadequacies of current recovery and disposal methods for mixed plastic wastes drive the exploration of viable strategies for plastics resource recovery. The combination of diminishing landfill space and increasing usage of plastic products poses a significant dilemma, since current recovery methods are costly and ill-suited to handle contaminants. Coprocessing of polymeric waste with other materials may provide potential solutions to the deficiencies of current resource recovery methods, including unfavorable process economics. By incorporating plastic waste as a minor feed into an existing process, variations in supply and composition could be mediated, permitting continuous operation. One attractive option is the coprocessing of polymeric waste with coal under direct liquefaction conditions, allowing for simultaneous conversion of both feedstocks into high-valued products. Catalyst-directed coliquefaction of coal and polymeric materials not only has attractive environmental implications but also has the potential to enhance the economic viability of traditional liquefaction processes. By exploiting the higher H/C ratio of the polymeric material and using it as a hydrogen source, the overall process demand for molecular hydrogen and hydrogen donor solvents may be reduced. A series of model compound experiments has been conducted, providing a starting point for unraveling the complex chemistry underlying coliquefaction of coal and polymeric materials. Tetradecane (C{sub 14} H{sub 30} ) was used as a polyethylene mimic, and 4-(naphthylmethyl)bibenzyl (NBBM) was used as a coal model compound. Neat and binary mixture reactions of tetradecane and NBBM were carried out in an inert atmosphere at both low and high pressures to establish a thermal baseline for subsequent catalytic experiments. Work in the past six months has focused on analysis of light gaseous products for neat reactions of tetradecane, resulting in mass balances greater than 94%. The experimental protocol developed in the previous project period was used to conduct experiments at elevated pressures more representative of coal liquefaction conditions, and both neat and binary mixture reactions of tetradecane and NBBM were examined. Mechanistic modeling studies were also initiated in order to support and quantify the mechanistic ideas put forth to explain the experimental observations.

DR. LINDA J. BROADBELT; MATTHEW J. DE WITT

1998-03-20T23:59:59.000Z

104

Silica membranes for hydrogen separation from coal gas. Final report  

DOE Green Energy (OSTI)

This project is a continuation of a previous DOE-UCR project (DE-FG22- 89PC89765) dealing with the preparation of silica membranes highly permselective to hydrogen at elevated temperatures, suitable for hydrogen separation from coal gas. The membranes prepared in the previous project had very high selectivity but relatively low permeance. Therefore, the general objectives of this project were to improve the permeance of these membranes and to obtain fundamental information about membrane structure and properties. The specific objectives were: (1) to explore new silylation reagents and reaction conditions with the purpose of reducing the thickness and increasing the permeance of silica membranes prepared by chemical vapor deposition (CVD), (2) to characterize the membrane structure, (3) to delineate mechanism and kinetics of deposition, (4) to measure the permeability of silica layers at different extents of deposition, and (5) to mathematically model the relationship between structure and deposition kinetics.

Gavalas, G.R.

1996-01-01T23:59:59.000Z

105

Prediction of thermodynamic properties of coal derivatives  

Science Conference Proceedings (OSTI)

The purpose of this research program is to understand and model the effect of the different intermolecular forces on the thermodynamic properties of systems containing pure compounds and mixtures. The compounds under consideration vary considerably in size, shape and energy. Therefore in order to develop a theory capable of describing accurately the thermodynamic properties and phase behavior of such systems over a wide range of temperature and pressure, one has to take into account explicitly the differences in shape and size among the various compounds as well as the different type of intermolecular interactions. We have developed equations of state for pure-component chain molecules. We have shown that the excellent performance of complicated theories such as the Generalized Flory Dimer (GFD) theory can be mimicked by simpler equations, if certain assumptions for the shape parameters are made. We developed engineering correlations based on the GFD theory, using local composition theory to take into account the attractive contribution. We compared various methods for the calculation of the repulsive and attractive contributions against computer simulation data for hard and square-well chains, and experimental data from the literature. We also have studied microstructure and local order in fluids that contain asymmetric molecules. In addition, simple cubic equations of state have been applied to calculate physical and chemical-reaction equilibria in non-ideal systems. In order to obtain a better understanding of the intermolecular forces and to test some of our recent models, we have performed considerable experimental work. We used FT-IR to examine the self-association of aliphatic alcohols due to hydrogen bonding. In addition, FT-IR spectroscopy was used to investigate Lewis acid-base interactions between probe and entrainer-cosolvent molecules.

Donohue, M.D.

1992-11-01T23:59:59.000Z

106

Hydrogen separation by ceramic membranes in coal gasification. Final report  

SciTech Connect

The general objective of this project was to develop hydrogen permselective membranes for hydrogen production from coal gas. The project consisted of the following tasks: (i) membrane preparation and characterization, (ii) membrane stability testing, and (iii) analysis and economic evaluation of a membrane-assisted ammonia from coal process. Several oxides (SiO{sub 2}, TiO{sub 2}, Al{sub 2}O{sub 3}, B{sub 2}O{sub 3}) in dense (or nonporous) form were identified to be permselective to hydrogen at elevated temperatures. To obtain reasonable permeance it is necessary that the membrane consists of a thin selective layer of the dense oxide supported on or within the pores of a porous support tube (or plate). Early in the project we chose porous Vycor tubes (5mm ID, 7 mm OD, 40 {Angstrom} mean pore diameter) supplied by Corning Inc. as the membrane support. To form the permselective layer (SiO{sub 2}, TiO{sub 2}, Al{sub 2}O{sub 3}, B{sub 2}O{sub 3}) we employed chemical vapor deposition using the reaction of the chloride (SiCl{sub 4}, etc.) vapor and water vapor at high temperatures. Deposition of the selective layer was carried out in a simple concentric tube reactor comprising the porous support tube surrounded by a wider concentric quartz tube and placed in an electrically heated split tube furnace. In one deposition geometry (the opposing reactants or two-sided geometry) the chloride vapor in nitrogen carrier was passed through the inner tube while the water vapor also in nitrogen carrier was passed in the same direction through the annulus between the two tubes. In the other (two-sided) geometry the chloride-containing stream and the water-containing stream were both passed through the inner tube or both through the annulus.

Gavalas, G.R.

1993-08-01T23:59:59.000Z

107

Filtering coal-derived oil through a filter media precoated with particles partially solubilized by said oil  

DOE Patents (OSTI)

Solids such as char, ash, and refractory organic compounds are removed from coal-derived liquids from coal liquefaction processes by the pressure precoat filtration method using particles of 85-350 mesh material selected from the group of bituminous coal, anthracite coal, lignite, and devolatilized coals as precoat materials and as body feed to the unfiltered coal-derived liquid.

Rodgers, Billy R. (Concord, TN); Edwards, Michael S. (Knoxville, TN)

1977-01-01T23:59:59.000Z

108

EVALUATION OF DENSIFIED REFUSE DERIVED FUELS FOR USE IN PULVERIZED COAL-FIRED  

E-Print Network (OSTI)

EVALUATION OF DENSIFIED REFUSE DERIVED FUELS FOR USE IN PULVERIZED COAL-FIRED STEAM GENERATORS with coal. This paper discusses these successful tests and the feasibility of preparing a d-RDF which can be processed with coal using existing, unmodified coal handling equipment and fired in conventional pulverized

Columbia University

109

Bioconversion of coal-derived synthesis gas to liquid fuels. [Butyribacterium methylotrophicum  

DOE Green Energy (OSTI)

The use of coal-derived synthesis gas as an industrial feedstock for production of fuels and chemicals has become an increasingly attractive alternative to present petroleum-based chemicals production. However, one of the major limitations in developing such a process is the required removal of catalyst poisons such as hydrogen sulfide (H{sub 2}S), carbonyl sulfide (COS), and other trace contaminants from the synthesis gas. Purification steps necessary to remove these are energy intensive and add significantly to the production cost, particularly for coals having a high sulfur content such as Illinois coal. A two-stage, anaerobic bioconversion process requiring little or no sulfur removal is proposed, where in the first stage the carbon monoxide (CO) gas is converted to butyric and acetic acids by the CO strain of Butyribacterium methylotrophicum. In the second stage, these acids along with the hydrogen (H{sub 2}) gas are converted to butanol, ethanol, and acetone by an acid utilizing mutant of Clostridium acetobutylicum. 18 figs., 18 tabs.

Jain, M.K.

1991-01-01T23:59:59.000Z

110

Impact of hydrogen partial pressure on coal liquefaction. Final technical report  

DOE Green Energy (OSTI)

This program was conducted to determine the effects of hydrogen partial pressure on the SRC-I direct coal liquefaction process and SRC-I Demonstration Plant design. A native solvent was produced in quantity and slurried with Kentucky number 9 Mulford coal in a series of coal liquefaction runs under varying hydrogen gas rates, temperatures, residence times, and hydrogen partial pressures. The results showed that hydrogen partial pressure significantly affected product distribution; the magnitude of the effect was comparable to changes in temperature and residence time. Also, the impact of hydrogen partial pressure was enhanced by increases in both temperature and residence time. Operating at low hydrogen partial pressure did not show any apparent advantage; it reduced coal conversion, reduced oil yield, and had a detrimental effect on the yield distribution of other products. An increase in hydrogen partial pressure had the following effects: increased coal conversion; increased conversion of asphaltenes and preasphaltenes to lighter products; significantly increased the oil yield; increased light gas yields; decreased sulfur content in the SRC; increased hydrogen content of the recycle solvent; and increased hydrogen consumption. This study strongly suggests that further studies should be conducted to optimize the effects of hydrogen partial pressure on the process, both within and, preferably, beyond the constraints of the current basic SRC-I design, considering the major impact of this variable on the process. 10 references, 37 figures, 10 tables.

Kang, D.; Hoover, D.S.; Schweighardt, F.K.

1984-06-01T23:59:59.000Z

111

Demonstration of a Carbonate Fuel Cell on Coal Derived Gas  

E-Print Network (OSTI)

Several studies indicate that carbonate fuel cell systems have the potential to offer efficient, cost competitive, and environmentally preferred power plants operating on natural gas or coal derived gas (syn-gas). To date, however, no fuel cell system has run on actual syn-gas. Consequently, the Electric Power Research Institute (EPRI) has sponsored a 20 kW carbonate fuel cell pilot plant that will begin operating in March at Destec Energys coal gasification plant in Plaquemine, Louisiana. The primary purpose of the test is to determine the effect of syn-gas contaminants on the performance and life of the carbonate fuel cell. This paper will describe the project objectives, design aspects of the pilot facility, and the status of the project.

Rastler, D. M.; Keeler, C. G.; Chi, C. V.

1993-03-01T23:59:59.000Z

112

Bio-Derived Liquids to Hydrogen Distributed Reforming Targets  

E-Print Network (OSTI)

used the H2A model to analyze data and produce cost estimates. Conclusion: "...the hydrogen total cost the estimated range." Transition to Bio-Derived Liquids Independent Validation of progress towards 2006 interim. Bio-Derived Renewable Liquids Dist. Electrolysis Central Wind Electrolysis Biomass Gasification Solar

113

Development of alternative fuels from coal-derived syngas  

DOE Green Energy (OSTI)

The overall objectives of this program are to investigate potential technologies for the conversion of coal-derived synthesis gas to oxygenated fuels, hydrocarbon fuels, fuel intermediates, and octane enhancers, and to demonstrate the most promising technologies at DOE's LaPorte, Texas, Slurry Phase Alternative Fuels development Unit (AFDU). The program will initially involve a continuation of the work performed under the Liquid Phase Methanol Program but will later draw upon information and technologies generated in current and future DOE-funded contracts, as well as test commercially available catalysts. 1 fig., 3 tabs.

Not Available

1991-03-22T23:59:59.000Z

114

Evaluation of alternative uses of coal and coal-derived fuels: industry, government, and public viewpoints  

DOE Green Energy (OSTI)

This report covers a study by Battelle's Columbus Laboratories to identify viewpoints representative of various interest groups on alternative uses of coal and coal-derived fuels. The study was conducted for the ERDA Fossil Energy Department to provide background inputs to the R and D planning process. A series of nine structured workshops was conducted with selected representatives of the various interest groups. The individual workshops included representation of industrial and utility companies, state and federal governments, and public interest groups. Viewpoints were recorded on (1) the relative importance of five specific evaluation criteria, (2) the evaluation of seven fuel categories against the criteria, (3) a forecast of future fuel utilization by categories, and (4) suggested R and D emphasis for the fuel categories. This report, Volume I, is a summary and appraisal of workshop results. Volume II contains appendices with more detailed records from the workshops.

Locklin, D.W.; Malone, D.W.; Molnar, D.E.; Sander, L.K.; Morrison, D.L.

1975-11-17T23:59:59.000Z

115

Potential Application of Coal-Derived Fuel Gases for the Glass...  

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

Mitretek Technical Report Potential Application of Coal-Derived Fuel Gases for the Glass Industry: A Scoping Analysis December 2004 David Gray Salvatore Salerno Glen Tomlinson...

116

Research on Improving Low Rank Coal Caking Ability by Hydrogenation  

Science Conference Proceedings (OSTI)

The experiment of improving low rank coal caking ability was carried out in an autoclave within a temperature of (623 to 673)K and a initial pressure of (3 to 6) MPa, the heat time range is 30-50min, the results indicated that: according to moderate ... Keywords: low rank coal, caking ability, maceral specification, coal blending

Huang Peng; Li Wenbo; Zhao Yuan; Ai Jun

2011-02-01T23:59:59.000Z

117

Secretary of Energy and Rep. Chabot Highlight Clean Coal and Hydrogen  

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

and Rep. Chabot Highlight Clean Coal and and Rep. Chabot Highlight Clean Coal and Hydrogen Research and Tout America's Economic Growth in Ohio Secretary of Energy and Rep. Chabot Highlight Clean Coal and Hydrogen Research and Tout America's Economic Growth in Ohio October 10, 2006 - 9:08am Addthis CINCINNATI, OH - U.S. Department of Energy (DOE) Secretary Samuel W. Bodman today joined Rep. Steve Chabot (OH-1st) to tour the hydrogen and clean coal research laboratory at the University of Cincinnati (UC) highlighting the importance of science and technology in reducing our dependence on fossil fuels and touting America's robust economy. Secretary Bodman discussed President Bush's commitment through the American Competitiveness Initiative to invest more than $136 billion over 10 years to increase investments in

118

High-yield hydrogen production by catalytic gasification of coal or biomass  

DOE Green Energy (OSTI)

Gasification of coal or wood, catalyzed by soluble metallic cations to maximize reaction rates and hydrogen yields, offers a potential for large-scale, economical hydrogen production with near-commercial technology. With optimum reaction conditions and catalysts, product gas rich in both hydrogen and methane can be used in fuel cells to produce electricity at efficiencies nearly double those of conventional power plant. If plantation silvaculture techniques can produce wood at a raw energy cost competitive with coal, further enhancement of product gas yields may be possible, with zero net contribution of CO{sub 2} to the atmosphere.

Hauserman, W.B.

1992-01-01T23:59:59.000Z

119

Kinetics of catalyzed steam gasification of low-rank coals to produce hydrogen. Final report  

Science Conference Proceedings (OSTI)

The principal goal of coal char-steam gasification research is to establish the feasibility of low-rank coal gasification for hydrogen production. The program has focused on determining reaction conditions for maximum product gas hydrogen content and on evaluating process kinetics with and without catalyst addition. The high inherent reactivity of lignites and subbituminous coals, compared to coals of higher rank, make them the probable choice for use in steam gasification. An extensive matrix of char-steam gasification tests was performed in a laboratory-scale thermogravimetric analyzer (TGA) at temperatures of 700/sup 0/, 750/sup 0/, and 800/sup 0/C. Reaction conditions for these tests were based on the results of earlier work at UNDERC in which product gases from fixed-bed, atmospheric pressure, steam gasification at temperatures of 700/sup 0/ to 750/sup 0/C were found to contain 63 to 65 mole % hydrogen, with the remainder being carbon dioxide, carbon monoxide, and less than 1 mole % methane. Four low-rank coals and one bituminous coal were included in the TGA test matrix. Catalysts screened in the study included K/sub 2/CO/sub 3/, Na/sub 2/CO/sub 3/, trona, nahcolite, sunflower hull ash, and lignite ash. Results of this study showed uncatalyzed North Dakota and Texas lignites to be slightly more reactive than a Wyoming subbituminous coal, and 8 to 10 times more reactive than an Illinois bituminous coal. Several catalysts that substantially improved low-rank coal steam gasification rates included pure and mineral (trona and nahcolite) alkali carbonates. The reactivity observed when using trona and nahcolite to catalyze the steam gasification was the highest, at nearly 3.5 times that without catalysts. The use of these inexpensive, naturally-occurring, alkalis as gasification catalysts may result in elimination of the need for catalyst recovery in the hydrogen-from-coal process. 11 refs., 23 figs., 9 tabs.

Galegher, S.J.; Timpe, R.C.; Willson, W.G.; Farnum, S.A.

1986-06-01T23:59:59.000Z

120

Production of jet fuel from coal-derived liquids  

DOE Green Energy (OSTI)

Amoco and Lummus Crest are evaluating the process options and economics for upgrading the naphtha, crude phenols, and tar oil by-products from the Great Plains Coal Gasification Plant to jet fuels and other salable products. Analytical characterizations of these three by-products indicate the range of products that can be manufactured from each, and potential problems which could be encountered during refining. These characterizations, along with limited experimental data and Amoco's proprietary process models, were used to design conceptual processing schemes for maximizing the production of Grades JP-4, JP-8, and high density (JP-8X) jet fuels from the by-product liquids. In addition to the maximum jet fuel schemes, conceptual designs have also been formulated for maximizing profits from refining of the Great Plains by-products. Conceptual processing schemes for profitable production of JP-4, JP-8, and JP-8X have been developed, as has a maximum profit'' case. All four of these additional cases have now been transferred to Lummus for design and integration studies. Development of these schemes required the use of linear programming technology. This technology includes not only conventional refining processes which have been adapted for use with coal-derived liquids (e.g. hydrotreating, hydrocracking), but also processes which may be uniquely suited to the Great Plains by-products such as cresylic acid extraction, hydordealkylation, and needle coking. 6 figs., 3 tabs.

Furlong, M.W.; Fox, J.D.; Masin, J.G.; Soderberg, D.J.

1987-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
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121

Development of alternative fuels from coal-derived syngas  

SciTech Connect

The overall objectives of this program are to investigate potential technologies for the conversion of coal-derived synthesis gas to oxygenated fuels, hydrocarbon fuels, fuel intermediates, and octane enhancers; and to demonstrate the most promising technologies at DOE's LaPorte, Texas, Slurry Phase Alternative Fuels Development Unit (AFDU). BASF continues to have difficulties in scaling-up the new isobutanol synthesis catalyst developed in Air Products' laboratories. Investigations are proceeding, but the proposed operation at LaPorte in April is now postponed. DOE has accepted a proposal to demonstrate Liquid Phase Shift (LPS) chemistry at LaPorte as an alternative to isobutanol. There are two principal reasons for carrying out this run. First, following the extensive modifications at the site, operation on a relatively benign'' system is needed before we start on Fischer-Tropsch technology in July. Second, use of shift catalyst in a slurry reactor will enable DOE's program on coal-based Fischer-Tropsch to encompass commercially available cobalt catalysts-up to now they have been limited to iron-based catalysts which have varying degrees of shift activity. In addition, DOE is supportive of continued fuel testing of LaPorte methanol-tests of MIOO at Detroit Diesel have been going particularly well. LPS offers the opportunity to produce methanol as the catalyst, in the absence of steam, is active for methanol synthesis.

Brown, D.M.

1992-05-19T23:59:59.000Z

122

Catalyzed steam gasification of low-rank coals to produce hydrogen  

Science Conference Proceedings (OSTI)

Advanced coal gasification technologies using low-rank coal is a promising alternative for meeting future demand for hydrogen. Steam gasification tests conducted at temperatures between 700/sup 0/ and 800/sup 0/C and atmospheric pressure resulted in product gas compositions matching those predicted by thermodynamic equilibrium calculations, 63-65 mol% hydrogen and less than 1 mol% methane. Steam gasification tests with four low-rank coals and a single bituminous coal were performed in a laboratory-scale thermogravimetric analyzer (TGA) at temperatures of 700/sup 0/, 750/sup 0/, and 800/sup 0/C to evaluate process kinetics with and without catalyst addition. Catalysts screened included K/sub 2/CO/sub 3/, Na/sub 2/CO/sub 3/, trona, nahcolite, sunflower hull ash, and recycled lignite ash. Uncatalyzed lignites and a subbituminous coal were found to be eight to ten times more reactive with steam at 700/sup 0/ to 800/sup 0/C than an Illinois bituminous coal. This relationship, within this narrow temperature range, is important as this is the range that thermodynamically favors the production of hydrogen from steam gasification at atmospheric pressure. The reactivity of the uncatalyzed coals increased 3 to 4 times with an increase in steam gasification temperature from 700/sup 0/ to 800/sup 0/C. For the catalyzed coals during steam gasification: Reactivity increased approximately 2 times over the 700/sup 0/ to 800/sup 0/C temperature range for low-rank coals catalyzed with potassium carbonate. Sodium carbonate was found to be as effective a catalyst as potassium carbonate for the steam gasification of low-rank coal chars on a mass loading basis; and naturally occurring mineral sources of sodium carbonates/bicarbonates, trona and nahcolite, are as effective in catalyzing low-rank coal steam gasification as the pure carbonates. 18 refs., 6 figs., 2 tabs.

Sears, R.E.; Timpe, R.C.; Galegher, S.J.; Willson, W.G.

1986-04-01T23:59:59.000Z

123

Refinery Integration of By-Products from Coal-Derived Jet Fuels  

Science Conference Proceedings (OSTI)

This report summarizes the accomplishments toward project goals during the no cost extension period of the third year of the project to assess the properties and performance of coal based products. These products are in the gasoline, diesel and fuel oil range and result from coal based jet fuel production from an Air Force funded program. Specific areas of progress include generation of coal based material that has been fractionated into the desired refinery cuts for a third round of testing, the use of a research gasoline engine to test coal-based gasoline, and modification of diesel engines for use in evaluating diesel produced in the project. At the pilot scale, the hydrotreating process was modified to separate the heavy components from the LCO and RCO fractions before hydrotreating in order to improve the performance of the catalysts in further processing. Hydrotreating and hydrogenation of the product has been completed, and due to removal of material before processing, yield of the jet fuel fraction has decreased relative to an increase in the gasoline fraction. Characterization of the gasoline fuel indicates a dominance of single ring alkylcycloalkanes that have a low octane rating; however, blends containing these compounds do not have a negative effect upon gasoline when blended in refinery gasoline streams. Characterization of the diesel fuel indicates a dominance of 3-ring aromatics that have a low cetane value; however, these compounds do not have a negative effect upon diesel when blended in refinery diesel streams. Both gasoline and diesel continue to be tested for combustion performance. The desulfurization of sulfur containing components of coal and petroleum is being studied so that effective conversion of blended coal and petroleum streams can be efficiently converted to useful refinery products. Activated carbons have proven useful to remove the heavy sulfur components, and unsupported Ni/Mo and Ni/Co catalysts have been very effective for hydrodesulfurization. Equipment is now in place to begin fuel oil evaluations to assess the quality of coal based fuel oil. Combustion and characterization of the latest fuel oil (the high temperature fraction of RCO from the latest modification) indicates that the fraction is heavier than a No. 6 fuel oil. Combustion efficiency on our research boiler is {approx}63% for the heavy RCO fraction, lower than the combustion performance for previous co-coking fuel oils and No. 6 fuel oil. Emission testing indicates that the coal derived material has more trace metals related to coal than petroleum, as seen in previous runs. An additional coal has been procured and is being processed for the next series of delayed co-coking runs. The co-coking of the runs with the new coal have begun, with the coke yield similar to previous runs, but the gas yield is lower and the liquid yield is higher. Characterization of the products continues. Work continues on characterization of liquids and solids from co-coking of hydrotreated decant oils; liquid yields include more saturated and hydro- aromatics, while the coke quality varies depending on the conditions used. Pitch material is being generated from the heavy fraction of co-coking.

Caroline E. Burgess Clifford; Andre Boehman; Chunshan Song; Bruce Miller; Gareth Mitchell

2007-03-17T23:59:59.000Z

124

SYNTHESIS OF METHYL METHACRYLATE FROM COAL-DERIVED SYNGAS  

DOE Green Energy (OSTI)

Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. The research team has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, we are currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last quarter (January-March/99), in-situ formaldehyde generation and condensation with methyl propionate were tested over various catalysts and reaction conditions. The patent application is in preparation and the results are retained for future reports.

Makarand R. Gogate; James J. Spivey; Joseph R. Zoeller; Richard D. Colberg; Gerald N. Choi; Samuel S. Tam

1999-04-21T23:59:59.000Z

125

Changes in hydrogen utilization with temperature during direct coal liquefaction  

Science Conference Proceedings (OSTI)

A reliable means of monitoring the major pathways of hydrogen utilization, in contrast to only measuring net hydrogen comsumption, would be very useful for process optimization. The goal of this work was to develop an analytical approach for quantitatively distinguishing hydrogen consumed in hydrogenation from that utilized to stabilize thermolysis fragments. The approach outlined yields a rather detailed description of the net utilization of hydrogen during direct liquefaction, partitioning it into contributions from gas generation, heteroatom removal, hydrogenation, and matrix breakdown. Preliminary results indicate that internal hydrogen reorganization, with little consumption, predominates at low temperatures, with hydrogenation being compensated for by the hydrogen liberated in condensations. As the temperature is increased, bond cleavage reactions and aromatization reactions appear to become more important, and the net hydrogen consumption increases. (3 tables 1 figs., 11 refs.)

Finseth, D.H.; Bockrath, B.C.; Cillo, D.L.; Illig, E.G.; Sprecher, R.F., Retcofsky, H.L.; Lett, R.G.

1983-01-01T23:59:59.000Z

126

Molecular catalytic hydrogenation of aromatic hydrocarbons and hydrotreating of coal liquids.  

Science Conference Proceedings (OSTI)

This report presents the results of research on the development of new catalytic pathways for the hydrogenation of multiring aromatic hydrocarbons and the hydrotreating of coal liquids at The University of Chicago under DOE Contract No. DE-AC22-91PC91056. The work, which is described in three parts, is primarily concerned with the research on the development of new catalytic systems for the hydrogenation of aromatic hydrocarbons and for the improvement of the quality of coal liquids by the addition of dihydrogen. Part A discusses the activation of dihydrogen by very basic molecular reagents to form adducts that can facilitate the reduction of multiring aromatic hydrocarbons. Part B examines the hydrotreating of coal liquids catalyzed by the same base-activated dihydrogen complexes. Part C concerns studies of molecular organometallic catalysts for the hydrogenation of monocyclic aromatic hydrocarbons under mild conditions.

Yang, Shiyong; Stock, L.M.

1996-05-01T23:59:59.000Z

127

COAL/POLYMER COPROCESSING WITH EFFICIENT USE OF HYDROGEN  

DOE Green Energy (OSTI)

The final project period was devoted to investigating the binary mixture pyrolysis of polypropylene and polystyrene. Their interactions were assessed in order to provide a baseline for experiments with multicomponent mixtures of polymers with coal. Pyrolysis of polypropylene, polystyrene and their binary mixture was investigated at temperatures of 350 C and 420 C with reaction times from 1 to 180 minutes. Two different loadings, 10 mg and 20 mg, were studied for neat polypropylene and polystyrene to assess the effect of total pressure on product yields and selectivities. For neat pyrolysis of polypropylene, total conversion was much higher at 420 C, and no significant effect of loading on the total conversion was observed. Four classes of products, alkanes, alkenes, dienes, and aromatic compounds, were observed, and their distribution was explained by a typical free radical mechanism. For neat polystyrene pyrolysis, conversion reached approximately 75% at 350 C, while at 420 C the conversion reached a maximum around 90% at 10 minutes and decreased at longer times because of condensation reactions. The selectivities to major products were slightly different for the two different loadings due to the effect of total reaction pressure on secondary reactions. For binary mixture pyrolysis, the overall conversion was higher than the average of the two neat cases. The conversion of polystyrene remained the same, but a significant enhancement in the polypropylene conversion was observed. This suggests that the less reactive polypropylene was initiated by polystyrene-derived radicals. These results are summarized in detail in an attached manuscript that is currently in preparation. The other results obtained during the lifetime of this grant are documented in the set of attached manuscripts.

Dr. Linda J. Broadbelt; Matthew J. DeWitt; Hsi-Wu Wong

2000-09-30T23:59:59.000Z

128

Homogeneous catalytic hydrogenations of complex carbonaceous substrates. [16 references  

SciTech Connect

Results of homogeneous catalytic hydrogenation of complex unsaturated substrates including coal and coal-derived materials are reported, with organic soluble molecular complexes as catalysts. Among the substrates used were Hvab coal, solvent-refined coal, and COED pyrolysate. The hydrogenations were carried out in an autoclave. The results are summarized in tables.

Cox, J L; Wilcox, W A; Roberts, G L

1976-11-05T23:59:59.000Z

129

Catalyzed steam gasification of low-rank coals to produce hydrogen  

Science Conference Proceedings (OSTI)

Advance coal gasification technologies using low-rank coal is a promising alternative for meeting future demand for hydrogen. Steam gasification tests conducted at temperatures between 700/sup 0/ and 800/sup 0/C and atmospheric pressure resulted in product gas compositions matching those predicted by thermodynamic equilibrium calculations, 63-65 mol% hydrogen and less then 1 mol% methane. Steam gasification tests with four low-rank coals and a single bituminous coal were performed in a laboratory-scale thermogravimetric analyzer (TGA) at temperatures of 700/sup 0/, 750/sup 0/, and 800/sup 0/C to evaluate process kinetics with and without catalyst addition. Catalysts screened included K/sub 2/CO/sub 3/, Na/sub 2/CO/sub 3/, trona, nahcolite, sunflower hull ash, and recycled lignite ash. North Dakota and Texas lignite chars were slightly more reactive than a Wyoming subbituminous coal char and eight to ten times more reactive than an Illinois bituminous coal char. Pure and mineral (trona nd nahcolite) alkali carbonates and recycled ash from K/sub 2/CO/sub 3/-catalyzed steam gasification tests substantially improved low-rank coal steam gasification rates. The reactivities obtained using trona and nahcolite to catalyze the steam gasification were the highest, at nearly 3.5 times those without catalysts.

Sears, R.E.; Timpe, R.C.; Galegher, S.J.; Willson, W.G.

1986-01-01T23:59:59.000Z

130

Synthesis of Methyl Methacrylate from Coal-Derived Syngas  

Science Conference Proceedings (OSTI)

Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. RTI has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, RTI is currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last month, RTI has finalized the design of a fixed-bed microreactor system for DME partial oxidation reactions. RTI incorporated some design changes to the feed blending system, so as to be able to blend varying proportions of DME and oxygen. RTI has also examined the flammability limits of DME-air mixtures. Since the lower flammability limit of DME in air is 3.6 volume percent, RTI will use a nominal feed composition of 1.6 percent in air, which is less than half the lower explosion limit for DME-air mixtures. This nominal feed composition is thus considered operationally safe, for DME partial oxidation reactions. RTI is also currently developing an analytical system for DME partial oxidation reaction system.

Gerald N. Choi; James J. Spivey; Jospeh R. Zoeller; Makarand R. Gogate; Richard D. Colberg; Samuel S. Tam

1998-04-17T23:59:59.000Z

131

University Coal Research | Department of Energy  

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

Science & Innovation Clean Coal Crosscutting Research University Coal Research University Coal Research Clean Coal Turbines Gasification Fuel Cells Hydrogen from Coal Coal...

132

Trace component analysis of process hydrogen streams at the Wilsonville Advanced Coal Liquefaction Facility  

DOE Green Energy (OSTI)

This report summarizes subcontracted work done by the Radian Corporation to analyze trace components in process hydrogen streams at the Advanced Coal Liquefaction Facility in Wilsonville, Alabama. The data will be used to help define whether the gas streams to be treated in the hydrogen processing unit in the SRC-I Demonstration Plant will require further treatment to remove trace contaminants that could be explosive under certain conditions. 2 references.

Bronfenbrenner, J.C.

1983-09-01T23:59:59.000Z

133

Production of hydrogen from low-rank coals: (Task 6. 1)  

SciTech Connect

The principal goal of this research project is to establish the feasibility of low-rank coal gasification for low-cost hydrogen production. This research involves a proof-of-concept and the early stages of engineering development using a continuous process unit (CPU). In parallel with this process development work, an evaluation of the relationship between the fundamental properties of low-rank coals and their reactivity under hydrogen-producing conditions is also being conducted. A 20--40 lb/hr fluid-bed gasifier (FBG) CPU was commissioned during this time period and has logged over 400 hours of operation during shakedown and operability testing. Maximum hydrogen production rates from the operability testing were over 17 SCF/lb MAF coal for both Wyodak and Velva test coals with a limestone bed, and for Martin Lake coal using 10 wt % trona, at 800{degree}C and a 2:1 steam:carbon ratio to 2:1 and increased with bed temperature over the range of 700{degree} to 800{degree}C. Agglomeration of the bed material when using trona as the catalyst was an operation problem during the CPU operability testing. The char of the low-rank coals was four to six times more reactive than that of the bituminous coal tested in the laboratory using thermogravimetric analysis (TGA). Surface analysis of the chars showed that the uniform distribution of K{sub 2}CO{sub 3} catalyst decreased with increasing coal rank. 8 refs., 17 figs., 16 tabs.

Sears, R.E.; Timpe, R.C.; Musich, M.A.; Cisney, S.J.

1988-04-01T23:59:59.000Z

134

COAL/POLYMER COPROCESSING WITH EFFICIENT USE OF HYDROGEN  

DOE Green Energy (OSTI)

Environmental and economical concerns over diminishing landfill space and the growing abundance of mixed plastic waste mandate development of viable strategies for recovering high-valued resources from waste polymers. Co-processing of waste polymer mixtures with coal allows for the simultaneous conversion of coal and plastics into high-valued fuels. However, there is limited information about the underlying reaction pathways, kinetics, and mechanisms controlling coal liquefaction in the presence of polymeric materials. A series of model compound experiments has been conducted, providing a starting point for unraveling the complex, underlying chemistry. Neat pyrolysis studies of model compounds of polyethylene and coal were conducted in batch reactors. Tetradecane (C{sub 14} H{sub 30} ) was used as a polyethylene mimic, and 4-(naphthylmethyl)bibenzyl (NBBM) was used as a coal model compound. Reaction temperatures were 420 and 500 C, and batch reaction times ranged from 5--150 minutes. Detailed product analysis using gas chromatography and mass spectrometry enabled the reactant conversion and product selectivities to be determined. Reaction of single components and binary mixtures allowed the kinetic coupling between feedstocks to be examined.

DR. LINDA J. BROADBELT; MATTHEW J. DE WITT

1997-03-20T23:59:59.000Z

135

Tire-Derived Fuel Cofiring Test in a Pulverized Coal Utility Boiler  

Science Conference Proceedings (OSTI)

Several utilities are cofiring tire-derived fuel (TDF) with coal and other fuels in stoker, fluidized-bed, and cyclone-fired boilers. The field tests described in this report provide data on and will be of interest to utilities evaluating TDF cofiring in pulverized coal (PC) boilers.

1995-02-08T23:59:59.000Z

136

ass combustion CO2 capture coal conversion mat on biofuels geologic storage hydrogen renewables  

E-Print Network (OSTI)

ass combustion CO2 capture coal conversion mat on biofuels geologic storage hydrogen renewables storage fuel cells CO2 capture photovoltaics ma conversion biofuels batteries conversion biofuels stion CO Stanford University About GCEP #12;Explored novel approaches for enhanced biofuel production, such as

Nur, Amos

137

Bioconversion of coal-derived synthesis gas to liquid fuels. Final technical report, September 1, 1990--August 31, 1991  

DOE Green Energy (OSTI)

The use of coal-derived synthesis gas as an industrial feedstock for production of fuels and chemicals has become an increasingly attractive alternative to present petroleum-based chemicals production. However, one of the major limitations in developing such a process is the required removal of catalyst poisons such as hydrogen sulfide (H{sub 2}S), carbonyl sulfide (COS), and other trace contaminants from the synthesis gas. Purification steps necessary to remove these are energy intensive and add significantly to the production cost, particularly for coals having a high sulfur content such as Illinois coal. A two-stage, anaerobic bioconversion process requiring little or no sulfur removal is proposed, where in the first stage the carbon monoxide (CO) gas is converted to butyric and acetic acids by the CO strain of Butyribacterium methylotrophicum. In the second stage, these acids along with the hydrogen (H{sub 2}) gas are converted to butanol, ethanol, and acetone by an acid utilizing mutant of Clostridium acetobutylicum. 18 figs., 18 tabs.

Jain, M.K.

1991-12-31T23:59:59.000Z

138

EVALUATION OF COAL-DERIVED LIQUIDS AS BOILER FUELS Volume 1  

Science Conference Proceedings (OSTI)

A combustion demonstration using six coal-derived liquid fuels indicated that these fuels are suitable for use in utility boilers. These fuels, exhibiting acceptable emissions and performance, would require only minimal fuel system modifications.

1985-09-20T23:59:59.000Z

139

EVALUATION OF COAL-DERIVED LIQUIDS AS BOILER FUELS Volume 4  

Science Conference Proceedings (OSTI)

A combustion demonstration using six coal-derived liquid fuels indicated that these fuels are suitable for use in utility boilers. These fuels, exhibiting acceptable emissions and performance, would require only minimal fuel system modifications.

1985-09-24T23:59:59.000Z

140

EVALUATION OF COAL-DERIVED LIQUIDS AS BOILER FUELS Volume 3  

Science Conference Proceedings (OSTI)

A combustion demonstration using six coal-derived liquid fuels indicated that these fuels are suitable for use in utility boilers. These fuels, exhibiting acceptable emissions and performance, would require only minimal fuel system modifications.

1985-09-24T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

EVALUATION OF COAL-DERIVED LIQUIDS AS BOILER FUELS Volume 5  

Science Conference Proceedings (OSTI)

A combustion demonstration using six coal-derived liquid fuels indicated that these fuels are suitable for use in utility boilers. These fuels, exhibiting acceptable emissions and performance, would require only minimal fuel system modifications.

1985-09-20T23:59:59.000Z

142

EVALUATION OF COAL-DERIVED LIQUIDS AS BOILER FUELS Volume 2  

Science Conference Proceedings (OSTI)

A combustion demonstration using six coal-derived liquid fuels indicated that these fuels are suitable for use in utility boilers. These fuels, exhibiting acceptable emissions and performance, would require only minimal fuel system modifications.

1985-09-19T23:59:59.000Z

143

Synthesis of acrylates and Methacrylates from Coal-Derived Syngas  

Science Conference Proceedings (OSTI)

Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas, under a contract from the U.S. Department of Energy, Federal Energy Technology Center. This three-step process consists of synthesis of a propionate, its condensation with formaldehyde, and esterification of resulting methacrylic acid (MAA) with methanol to produce MMA. Eastman has focused on the propionate synthesis step. The resultant Mo catalysts work efficiently at much less severe conditions (170{degrees}C and 30 atm) than the conventional Ni catalysts (270{degrees} C and 180 atm). Bechtel has performed an extensive cost analysis which shows that Eastman`s propionate synthesis step is competitive with other technologies to produce the anhydride. Eastman and Bechtel have also compared the RTI- Eastman-Bechtel three-step methanol route to five other process routes to MMA. The results show that the product MMA can be produced at 520/lb, for a 250 Mlb/year MMA plant, and this product cost is competitive to all other process routes to MMA, except propyne carbonylation. In the second step, RTI and Eastman have developed active and stable V-SI-P tertiary metal oxide catalysts, Nb/Si0{sub 2}, and Ta/Si0{sub 2} catalysts for condensation of propionic anhydride or propionic acid with formaldehyde. RTI has demonstrated a novel correlation among the catalyst acid-base properties, condensation reaction yield, and long-term catalyst performance. Eastman and Bechtel have used the RTI experimental results of a 20 percent Nb/Si0{sub 2} catalyst, in terms of reactant conversions, MAA selectivities, and MAA yield, for their economic analysis. Recent research focuses on enhancing the condensation reaction yields, a better understanding of the acid-base property correlation and enhancing the catalyst lifetime.

NONE

1997-05-12T23:59:59.000Z

144

Synthesis of Methyl Methacrylate From Coal-Derived Syngas  

SciTech Connect

Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. RTI has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, RTI is currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last quarter(April-June, 1998), RTI has modified the reactor system including a new preheater and new temperature settings for the preheater. Continuous condensation of formaldehyde with propionic acid were carried out over 10% Nb O /SiO at 300C without 2 5 2 interruption. Five activity and four regeneration cycles have been completed without plugging or material balance problems. The results show that 10% Nb O /SiO deactivates slowly with time 2 5 2 but can be regenerated, at least four times, to 100% of its original activity with 2% O in nitrogen 2 at 400C. The cycles continue with consistent 90-95% of carbon balance. The reaction is scheduled to complete with 6 activity cycles and 5 regenerations. Used catalysts will be analyzed with TGA and XPS to determine bulk and surface coke content and coke properties. RTI will start the investigation of effects of propionic acid/formaldehyde ratio on reaction activity and product selectivity over 20% Nb O /SiO catalysts.

Ben W.-L. Jang; Gerald N. Choi; James J. Spivey; Jospeh R. Zoeller; Richard D. Colberg; Samuel S. Tam

1998-07-27T23:59:59.000Z

145

CAPITAL AND OPERATING COST OF HYDROGEN PRODUCTION FROM COAL GASIFICATI...  

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

8 Coal Using Preliminary Assumptions 2-15 2.5.1 Approach to Cost Estimating 2-16 2.5.2 Production Costs (Operation and Maintenance) 2-16 2.5.3 Consumables 2-17 2.5.4 Byproduct...

146

Catalytic Process for the Conversion of Coal-derived Syngas to Ethanol  

Science Conference Proceedings (OSTI)

The catalytic conversion of coal-derived syngas to C{sub 2+} alcohols and oxygenates has attracted great attention due to their potential as chemical intermediates and fuel components. This is particularly true of ethanol, which can serve as a transportation fuel blending agent, as well as a hydrogen carrier. A thermodynamic analysis of CO hydrogenation to ethanol that does not allow for byproducts such as methane or methanol shows that the reaction: 2 CO + 4 H{sub 2} {yields} C{sub 2}H{sub 5}OH + H{sub 2}O is thermodynamically favorable at conditions of practical interest (e.g,30 bar, {approx}Fischer-Tropsch catalysts, or (d) Mo-sulfides and phosphides. This project focuses on Rh- and Cu-based catalysts. The logic was that (a) Rh-based catalysts are clearly the most selective for EtOH (but these catalysts can be costly), and (b) Cu-based catalysts appear to be the most selective of the non-Rh catalysts (and are less costly). In addition, Pd-based catalysts were studied since Pd is known for catalyzing CO hydrogenation to produce methanol, similar to copper. Approach. The overall approach of this project was based on (a) computational catalysis to identify optimum surfaces for the selective conversion of syngas to ethanol; (b) synthesis of surfaces approaching these ideal atomic structures, (c) specialized characterization to determine the extent to which the actual catalyst has these structures, and (d) testing at realistic conditions (e.g., elevated pressures) and differential conversions (to measure true kinetics, to avoid deactivation, and to avoid condensable concentrations of products in the outlet gas).

James Spivery; Doug Harrison; John Earle; James Goodwin; David Bruce; Xunhau Mo; Walter Torres; Joe Allison Vis Viswanathan; Rick Sadok; Steve Overbury; Viviana Schwartz

2011-07-29T23:59:59.000Z

147

Evaluation of biological conversion of coal-derived synthesis gas  

DOE Green Energy (OSTI)

Foster Wheeler USA Corporation conducted an evaluation study on the biological conversion of synthesis gas to methane which is under development at the University of Arkansas. A conceptual design of an integrated coal-based SNG plant, employing the bioconversion process route, was developed together with the corresponding capital and operating costs. The economics were compared to those for a coal-based SNG plant design using the conventional catalytic route for shift and methanation. 5 refs., 10 figs., 22 tabs.

Fu, R.K.; Mazzella, G.

1990-09-01T23:59:59.000Z

148

Electrochemical polishing of hydrogen sulfide from coal synthesis gas  

DOE Green Energy (OSTI)

An advanced process has been developed for the separation of H{sub 2}S from coal gasification product streams through an electrochemical membrane. This technology is developed for use in coal gasification facilities providing fuel for cogeneration coal fired electrical power facilities and Molten Carbonate Fuel Cell electrical power facilities. H{sub 2}S is removed from the syn-gas by reduction to the sulfide ion and H at the cathode. The sulfide ion migrates to the anode through a molten salt electrolyte suspended in an inert ceramic matrix. Once at the anode it is oxidized to elemental sulfur and swept away for condensation in an inert gas stream. The syn-gas is enriched with the H{sub 2}. Order-of-magnitude reductions in H{sub 2}S have been repeatably recorded (100 ppm to 10 ppm H{sub 2}S) on a single pass through the cell. This process allows removal of H{sub 2}S without cooling the gas stream and with negligible pressure loss through the separator. Since there are no absorbents used, there is no absorption/regeneration step as with conventional technology. Elemental sulfur is produced as a by-product directly, so there is no need for a Claus process for sulfur recovery. This makes the process economically attractive since it is much less equipment intensive than conventional technology.

Gleason, E.F.; Winnick, J.

1995-11-01T23:59:59.000Z

149

Biomass-Derived Hydrogen from a Thermally Ballasted Gasifier  

DOE Green Energy (OSTI)

The goal of this project is to develop an indirectly heated gasification system that converts switchgrass into hydrogen-rich gas suitable for powering fuel cells. The project includes investigations of the indirectly-heated gasifier, development of particulate removal equipment, evaluation of catalytic methods for upgrading producer gas, development of contaminant measurement and control techniques, modeling of the thermal performance of the ballasted gasifier, and estimation of the cost of hydrogen from the proposed gasification system. Specific technologies investigated include a thermally ballasted gasifier, a moving bed granular filter, and catalytic reactors for steam reforming and water-gas shift reaction. The approach to this project was to employ a pilot-scale (5 ton per day) gasifier to evaluate the thermally ballasted gasifier as a means for producing hydrogen from switchgrass. A slipstream from the gasifier was used to evaluate gas cleaning and upgrading options. Other tests were conducted with laboratory-scale equipment using simulated producer gas. The ballasted gasifier operated in conjunction with a steam reformer and two-stage water-gas shift reactor produced gas streams containing 54.5 vol-% H2. If purge gas to the feeder system could be substantially eliminated, hydrogen concentration would reach 61 vol-%, which closely approaches the theoretical maximum of 66 vol-%. Tests with a combined catalyst/sorbent system demonstrated that steam reforming and water-gas shift reaction could be substantially performed in a single reactor and achieve hydrogen concentrations exceeding 90 vol-%. Cold flow trials with a laboratory-scale moving bed granular filter achieved particle removal efficiencies exceeding 99%. Two metal-based sorbents were tested for their ability to remove H2S from biomass-derived producer gas. The ZnO sorbent, tested at 450? C, was effective in reducing H2S from 200 ppm to less than 2 ppm (>99% reduction) while tests with the MnO sorbent were inconclusive. A computer model was developed that successfully predicted the thermal performance of the ballasted gasifier. An economic comparison of an air-blown gasification plant and a ballasted gasifier plant found that operating costs for ballasted gasification plant are about 31% higher than for the air blown gasifier plant. Hydrogen from the ballasted gasification plant and air blown gasification plant are projected to be $2.43/kg and $1.85/kg, respectively. This is lower than U.S. DOEs 2010 target price of $2.90/kg and comparable to U.S. DOEs 2015 target price of $2.00/kg.

Robert C. Brown

2007-04-06T23:59:59.000Z

150

Hydrogen separation by ceramic membranes in coal gasification  

DOE Green Energy (OSTI)

Table 1 lists the support tubes and the deposition reactants and other conditions used to prepare seven membranes. The permeances of these membranes immediately after deposition, after twelve hours of thermal treatment at 700--750{degrees}C, and after thirteen days of additional hydrothermal treatment at 550{degrees}C under 3 atm of water vapor are listed in Table 2. Figure 1 is an Arrhenius plot of the hydrogen permeance of membrane D25 (dimer reactant, 25 A pore support) before and after the hydrothermal treatment. The following conclusions can be drawn from the results of Tables 1 and 2. All membranes prepared in this series underwent hydrothermal treatment with the expected decrease of hydrogen permeance. Using the dimer and trimer precursors resulted in a slight improvement in hydrogen permeance and had no consistent effect on the H{sub 2}:N{sub 2} selectivity. Using the 25 {Angstrom} pore tubes improved moderately the hydrogen permeance but seemingly reduced the selectivity from about 500--1000 to about 200--300. The best permeance was obtained with membrane D25 made with 25 {Angstrom} pore size tubes using the dimer precursor. This tube had hydrogen permeance 0.13 Cm{sup 3}/Cm{sup 2}-min-atm and H{sub 2}:N{sub 2} selectivity of 200 at 500{degrees}C, after the thirteen-day hydrothermal treatment. It must be noted that the measurement of the very small nitrogen permeance is subject to considerable error, especially if there is some small leak in the system. Hence the true N{sub 2} permeances may be considerably lower than the measurements indicate, and the reported selectivities probably significantly underestimate the true selectivities. Figure 1 shows a sharp increase in the activation energy of hydrogen permeance following deposition and hydrothermal treatment.

Gavalas, G.R.

1992-11-01T23:59:59.000Z

151

SYNTHESIS OF METHYL METHACRYLATE FROM COAL-DERIVED SYNGAS  

DOE Green Energy (OSTI)

Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. RTI has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, RTI is currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last quarter (July-September, 1998), the project team has completed the continuous condensation of formaldehyde with propionic acid over 10% Nb{sub 2}O{sub 5}/SiO{sub 2} at 300 C. Six activity and five regeneration cycles have been completed. The results show that 10% Nb{sub 2}O{sub 5}/SiO{sub 2} deactivates slowly with time but can be regenerated to its original activity with 2% O{sub 2} in nitrogen over night at 400 C. We have investigated the effects of regeneration, propionic acid/formaldehyde ratio (PA/HCHO = 4.5/1 to 1.5/1) and reaction temperature(280-300 C) on reaction activity and product selectivity over 20% Nb{sub 2}O{sub 5}/SiO{sub 2} catalysts. The regeneration effect on 20% Nb{sub 2}O{sub 5}/SiO{sub 2} is similar to the effect on 10% Nb{sub 2}O{sub 5}/SiO{sub 2}. The regeneration can bring the deactivated catalyst to its original activity. However, the selectivity to MAA decreases with regeneration while the selectivity to DEK and CO{sub 2} increases. When PA/HCHO ratio is decreased from 4.5/1 to 2.25/1 then to 1.5/1 at 300 C the MAA yield decreases but the MAA selectivity first increases then decreases. Decreasing the reaction temperature from 300 C to 280 C decreases the MAA yield from 39.5% to 30.7% but increases the MAA selectivity from 73.7% to 82.2%. The results indicate that both temperature and PA/HCHO ratio are important parameters to optimize the economic of the condensation between propionic acid and formaldehyde.

BEN W.-L. JANG; GERALD N. CHOI; JAMES J. SPIVEY; JOSPEH R. ZOELLER; RICHARD D. COLBERG

1998-10-20T23:59:59.000Z

152

Synthesis of Acrylates and Methacrylates from Coal-Derived Syngas.  

Science Conference Proceedings (OSTI)

Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas, under a contract from the U.S. Department of Energy/Federal Energy Technology Center (DOE/FETC). This three-step process consists of synthesis of a propionate, its condensation with formaldehyde, and esterification of resulting methacrylic acid (MAA) with methanol to produce MMA. Over the last quarter, RTI carried out activity tests on a pure (99 percent) Nb{sub 2}O{sub 5} catalyst, received from Alfa Aesar, under the following experimental conditions: T=300 C; P=4 atm, 72:38:16:4:220 mmol/h, PA:H{sub 2}0:HCHO:CH{sub 3}0H:N{sub 2}; 5-g catalyst charge. For the pure material, the MAA yields (based on HCHO and PA) were at 8.8 and 1.5 percent, clearly inferior compared to those for a 10-percent Nb{sub 2}O{sub 5}/Si0{sub 2} catalyst (20.1 and 4.5 percent). The X-ray diffraction (XRD) patterns of pure Nb{sub 2}O{sub 5} and 20-percent Nb{sub 2}O{sub 5}/Si0{sub 2} that while pure Nb{sub 2}O{sub 5} is very highly crystalline, Si0{sub 2} support for an amorphous nature of the 20 percent Nb{sub 2}O{sub 5}/Si0{sub 2} catalyst the last quarter, RTI also began research on the use of dimethyl ether (DME), product of methanol dehydrocondensation, as an alternate feedstock in MMA synthesis. As a result, formaldehyde is generated either externally or in situ, from DME, in the process envisaged in the contract extension. The initial work on the DME extension of the contract focuses on a tradeoff analysis that will include a preliminary economic analysis of the DME and formaldehyde routes and catalyst synthesis and testing for DME partial oxidation and condensation reactions. Literature guides exist for DME partial oxidation catalysts; however, there are no precedent studies on catalyst development for DME-methyl propionate (MP) condensation reactions, thereby making DME-MP reaction studies a challenge. The design of a fixed-bed microreactor system for DME feedstock studies was also finalized over the last quarter. The system is designed to be operated either in DME partial oxidation mode (for formaldehyde synthesis) or DME-MP condensation mode (for MMA synthesis).

Gogate, M.R.; Spivey, J.J.; Zoeller, J.R.; Colberg, R.D.; Choi, G.N.; Tam, S.S.

1997-10-17T23:59:59.000Z

153

Investigations into coal coprocessing and coal liquefaction  

DOE Green Energy (OSTI)

The conversion of coal to liquid suitable as feedstock to a petroleum refinery is dependent upon several process variables. These variables include temperature, pressure, coal rank, catalyst type, nature of the feed to the reactor, type of process, etc. Western Research Institute (WRI) has initiated a research program in the area of coal liquefaction to address the impact of some of these variables upon the yield and quality of the coal-derived liquid. The principal goal of this research is to improve the efficiency of the coal liquefaction process. Two different approaches are currently being investigated. These include the coprocessing of a heavy liquid, such as crude oil, and coal using a dispersed catalyst and the direct liquefaction of coal using a supported catalyst. Another important consideration in coal liquefaction is the utilization of hydrogen, including both externally- and internally-supplied hydrogen. Because the incorporation of externally-supplied hydrogen during conversion of this very aromatic fossil fuel to, for example, transportation fuels is very expensive, improved utilization of internally-supplied hydrogen can lead to reducing processing costs. The objectives of this investigation, which is Task 3.3.4, Coal Coprocessing, of the 1991--1992 Annual Research Plan, are: (1) to evaluate coal/oil pretreatment conditions that are expected to improve the liquid yield through more efficient dispersion of an oil-soluble, iron-based catalyst, (2) to characterize the coke deposits on novel, supported catalysts after coal liquefaction experiments and to correlate the carbon skeletal structure parameters of the coke deposit with catalyst performance as measured by coal liquefaction product yield, and (3) to determine the modes of hydrogen utilization during coal liquefaction and coprocessing. Experimental results are discussed in this report.

Guffey, F.D.; Netzel, D.A.; Miknis, F.P.; Thomas, K.P. [Western Research Inst., Laramie, WY (United States); Zhang, Tiejun; Haynes, H.W. Jr. [Wyoming Univ., Laramie, WY (United States). Dept. of Chemical Engineering

1994-06-01T23:59:59.000Z

154

Apparatus and method for pumping hot, erosive slurry of coal solids in coal derived, water immiscible liquid  

SciTech Connect

An apparatus for and method of pumping hot, erosive slurry of coal solids in a coal derived, water immiscible liquid to higher pressure involves the use of a motive fluid which is miscible with the liquid of the slurry. The apparatus includes a pump 12, a remote check valve 14 and a chamber 16 between and in fluid communication with the pump 12 and check valve 14 through conduits 18,20. Pump 12 exerts pressure on the motive fluid and thereby on the slurry through a concentration gradient of coal solids within chamber 16 to alternately discharge slurry under pressure from the outlet port of check valve 14 and draw slurry in through the inlet port of check valve 14.

Ackerman, Carl D. (Olympia, WA)

1983-03-29T23:59:59.000Z

155

Development of Disposable Sorbents for Chloride Removal from High-Temperature Coal-Derived Gases  

Science Conference Proceedings (OSTI)

The integrated coal-gasification combined-cycle approach is an efficient process for producing electric power from coal by gasification, followed by high-temperature removal of gaseous impurities, then electricity generation by gas turbines. Alternatively, molten carbonate fuel cells (MCFC) may be used instead of gas turbine generators. The coal gas must be treated to remove impurities such as hydrogen chloride (HCl), a reactive, corrosive, and toxic gas, which is produced during gasification from chloride species in the coal. HCl vapor must be removed to meet environmental regulations, to protect power generation equipments such as fuel cells or gas turbines, and to minimize deterioration of hot coal gas desulfurization sorbents. The objectives of this study are to: (1) investigate methods to fabricate reactive sorbent pellets or granules that are capable of reducing HCl vapor in high-temperature coal gas streams to less than 1 ppm in the temperature range 400{degrees}C to 650{degrees}C and the pressure range 1 to 20 atm; (2) testing their suitability in bench-scale fixed- or fluidized-bed reactors; (3) testing a superior sorbent in a circulating fluidized- bed reactor using a gas stream from an operating coal gasifier; and (4) updating the economics of high temperature HCl removal.

Krishnan, G.N.; Canizales, A. [SRI International, Menlo Park, CA (United States); Gupta, R. [Research Triangle Inst., Research Triangle Park, NC (United States); Ayala, R. [General Electric Co., Schenectady, NY (United States). Corporate Research and Development Center

1996-12-31T23:59:59.000Z

156

Coal derived fuel gases for molten carbonate fuel cells  

DOE Green Energy (OSTI)

Product streams from state-of-the-art and future coal gasification systems are characterized to guide fuel cell program planners and researchers in establishing performance goals and developing materials for molten carbonate fuel cells that will be compatible with gasifier product gases. Results are presented on: (1) the range of gasifier raw-gas compositions available from the major classes of coal gasifiers; (2) the degree of gas clean-up achievable with state-of-the-art and future gas clean-up systems; and (3) the energy penalties associated with gas clean-up. The study encompasses fixed-bed, fluid-bed, entrained-bed, and molten salt gasifiers operating with Eastern bituminous and Western subbituminous coals. Gasifiers operating with air and oxygen blowing are evaluated, and the coal gasification product streams are characterized with respect to: (1) major gas stream constituents, e.g., CO, H/sub 2/, CO/sub 2/, CH/sub 4/, N/sub 2/, H/sub 2/O; (2) major gas stream contaminants, e.g., H/sub 2/S, COS, particulates, tars, etc.; and (3) trace element contaminants, e.g., Na, K, V, Cl, Hg, etc.

Not Available

1979-11-01T23:59:59.000Z

157

Bimetallic promotion of cooperative hydrogen transfer and heteroatom removal in coal liquefaction  

DOE Green Energy (OSTI)

The ultimate objective of this research has been to uncover novel reagents and experimental conditions for heteroatom removal and hydrogen transfer processes, which would be applicable to the liquefaction of coal under low-severity conditions. To this end, one phase of this research has investigated the cleavage of carbon-heteroatom bonds involving sulfur, oxygen, nitrogen and halogen by subvalent transition-metal complexes. A second phase of the study has assessed the capability of the same transition-metal complexes or of organoaluminum Lewis acids to catalyze the cleavage of carbon-hydrogen bonds in aromatics and hence to promote hydrogen shuttling. Finally, a third phase of our work has uncovered a remarkable synergistic effect of combinations of transition metals with organoaluminum Lewis acids on hydrogen shuttling between aromatics and hydroaromatics. (VC)

Eisch, J.J.

1992-04-07T23:59:59.000Z

158

Catalytic Process for the Conversion of Coal-derived Syngas to Ethanol  

DOE Green Energy (OSTI)

The catalytic conversion of coal-derived syngas to C{sub 2+} alcohols and oxygenates has attracted great attention due to their potential as chemical intermediates and fuel components. This is particularly true of ethanol, which can serve as a transportation fuel blending agent, as well as a hydrogen carrier. A thermodynamic analysis of CO hydrogenation to ethanol that does not allow for byproducts such as methane or methanol shows that the reaction: 2 CO + 4 H{sub 2} {yields} C{sub 2}H{sub 5}OH + H{sub 2}O is thermodynamically favorable at conditions of practical interest (e.g,30 bar, {approx}< 250 C). However, when methane is included in the equilibrium analysis, no ethanol is formed at any conditions even approximating those that would be industrially practical. This means that undesired products (primarily methane and/or CO{sub 2}) must be kinetically limited. This is the job of a catalyst. The mechanism of CO hydrogenation leading to ethanol is complex. The key step is the formation of the initial C-C bond. Catalysts that are selective for EtOH can be divided into four classes: (a) Rh-based catalysts, (b) promoted Cu catalysts, (c) modified Fischer-Tropsch catalysts, or (d) Mo-sulfides and phosphides. This project focuses on Rh- and Cu-based catalysts. The logic was that (a) Rh-based catalysts are clearly the most selective for EtOH (but these catalysts can be costly), and (b) Cu-based catalysts appear to be the most selective of the non-Rh catalysts (and are less costly). In addition, Pd-based catalysts were studied since Pd is known for catalyzing CO hydrogenation to produce methanol, similar to copper. Approach. The overall approach of this project was based on (a) computational catalysis to identify optimum surfaces for the selective conversion of syngas to ethanol; (b) synthesis of surfaces approaching these ideal atomic structures, (c) specialized characterization to determine the extent to which the actual catalyst has these structures, and (d) testing at realistic conditions (e.g., elevated pressures) and differential conversions (to measure true kinetics, to avoid deactivation, and to avoid condensable concentrations of products in the outlet gas).

James Spivery; Doug Harrison; John Earle; James Goodwin; David Bruce; Xunhau Mo; Walter Torres; Joe Allison Vis Viswanathan; Rick Sadok; Steve Overbury; Viviana Schwartz

2011-07-29T23:59:59.000Z

159

Novel, Magnetically Fluidized-Bed Reactor Development for the Looping Process: Coal to Hydrogen Production Research and Development  

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

Novel, Magnetically Fluidized-Bed Novel, Magnetically Fluidized-Bed Reactor Development for the Looping Process: Coal to Hydrogen Production Research and Development Background The U.S. Department of Energy (DOE) National Energy Technology Laboratory (NETL) is committed to improving methods for co-producing power and chemicals, fuels, and hydrogen (H2). Gasification is a process by which fuels such as coal can be used to produce synthesis gas (syngas), a mixture of H2, carbon monoxide (CO), and carbon

160

Hydrogen production by high-temperature steam gasification of biomass and coal  

Science Conference Proceedings (OSTI)

High-temperature steam gasification of paper, yellow pine woodchips, and Pittsburgh bituminous coal was investigated in a batch-type flow reactor at temperatures in the range of 700 to 1,200{sup o}C at two different ratios of steam to feedstock molar ratios. Hydrogen yield of 54.7% for paper, 60.2% for woodchips, and 57.8% for coal was achieved on a dry basis, with a steam flow rate of 6.3 g/min at steam temperature of 1,200{sup o}C. Yield of both the hydrogen and carbon monoxide increased while carbon dioxide and methane decreased with the increase in gasification temperature. A 10-fold reduction in tar residue was obtained at high-temperature steam gasification, compared to low temperatures. Steam and gasification temperature affects the composition of the syngas produced. Higher steam-to-feedstock molar ratio had negligible effect on the amount of hydrogen produced in the syngas in the fixed-batch type of reactor. Gasification temperature can be used to control the amounts of hydrogen or methane produced from the gasification process. This also provides mean to control the ratio of hydrogen to CO in the syngas, which can then be processed to produce liquid hydrocarbon fuel since the liquid fuel production requires an optimum ratio between hydrogen and CO. The syngas produced can be further processed to produce pure hydrogen. Biomass fuels are good source of renewable fuels to produce hydrogen or liquid fuels using controlled steam gasification.

Kriengsak, S.N.; Buczynski, R.; Gmurczyk, J.; Gupta, A.K. [University of Maryland, College Park, MD (United States). Dept. of Mechanical Engineering

2009-04-15T23:59:59.000Z

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161

Conversion system overview assessment. Volume III. Solar thermal/coal or biomass derived fuels  

SciTech Connect

The three volumes of this report cover three distinct areas of solar energy research: solar thermoelectrics, solar-wind hybrid systems, and synthetic fuels derived with solar thermal energy. Volume III deals with the conversion of synthetic fuels with solar thermal heat. The method is a hybrid combination of solar energy with either coal or biomass. A preliminary assessment of this technology is made by calculating the cost of fuel produced as a function of the cost of coal and biomass. It is shown that within the projected ranges of coal, biomass, and solar thermal costs, there are conditions when solar synthetic fuels with solar thermal heat will become cost-competitive.

Copeland, R. J.

1980-02-01T23:59:59.000Z

162

Coal....  

U.S. Energy Information Administration (EIA)

DOE EIA WEEKLY COAL ... Coal Prices and Earnings (updated April 28, 2004) Spot coal prices in the East rose steadily since Labor Day 2003, with rapid escalations ...

163

Coal....  

U.S. Energy Information Administration (EIA)

DOE EIA WEEKLY COAL ... Coal Prices and Earnings (updated September 26) The average spot prices for reported coal purchases rose once again ...

164

Mechanism of hydrogen incorporation in coal liquefaction: Fifteenth report, progress as of March 31, 1995  

DOE Green Energy (OSTI)

The authors continued work on the reaction of deuterium with coal model materials. Their recent efforts have emphasized models in which organic compounds are immobilized on the surface of silica. They have also carried out some studies on the effect of silica itself on the reaction with deuterium. Work in progress and results are described for the subtask entitled, Silica-catalyzed hydrogenations of alkenes.

NONE

1995-05-01T23:59:59.000Z

165

Chemistry and structure of coal-derived asphaltenes, Phase III. Quarterly progress report, January--March 1978  

SciTech Connect

The solubility limits of Synthoil and PAMCO asphaltenes have been measured as a function of Hildebrand solubility parameters and hydrogen bonding. Solvents with moderate hydrogen bonding capacity such as dioxane, ethyl benzoate and dibutyl phthalate were found to be most effective in dissolving asphaltenes over the widest range of solubility parameters. VPO molecular weight studies of coal liquid derived carbenes, as a function of concentration in the solvent THF, indicate that these fractions are more strongly self-associated than the corresponding asphaltenes, and generally afford high infinite dilution number average molecular weights: Synthoil, 861; HRI H-Coal, 1156; Cat. Inc. SRC, 1228; PAMCO SRC, 1054. The variable ESR temperature dependence of the spin intensity for a Synthoil asphaltene-I/sub 2/ charge transfer followed a 1/T (Curie--Weiss) dependence over the temperature range from 25/sup 0/ to -114/sup 0/C suggesting that independent, non-interacting donor and acceptor doublets were formed. Weight percent OH values, determined from 'H NMR analysis of silylated asphaltenes, were found to provide a reasonably linear correlation with the absorbance of the monomeric OH infrared stretching bands of the asphaltenes.

Yen, T. F.

1978-01-01T23:59:59.000Z

166

A novel and cost-effective hydrogen sulfide removal technology using tire derived rubber particles.  

E-Print Network (OSTI)

??Hydrogen sulfide (H2S) is corrosive, toxic, and produced during the anaerobic digestion process at wastewater treatment plants. Tire derived rubber particles (TDRPTM) and other rubber (more)

Siefers, Andrea Mary

2010-01-01T23:59:59.000Z

167

Comparison of coal/solid recovered fuel (SRF) with coal/refuse derived fuel (RDF) in a fluidised bed reactor  

Science Conference Proceedings (OSTI)

An experimental study was undertaken to compare the differences between municipal solid waste (MSW) derived solid recovered fuel (SRF) (complying with CEN standards) and refuse derived fuel (RDF). Both fuels were co-combusted with coal in a 50 kW fluidised bed combustor and the metal emissions were compared. Synthetic SRF was prepared in the laboratory by grinding major constituents of MSW such as paper, plastic, textile and wood. RDF was obtained from a local mechanical treatment plant. Heavy metal emissions in flue gas and ash samples from the (coal + 10% SRF) fuel mixture were found to be within the acceptable range and were generally lower than that obtained for coal + 10% RDF fuel mixture. The relative distribution of heavy metals in ash components and the flue gas stream shows the presence of a large fraction (up to 98%) of most of the metals in the ash (except Hg and As). Thermo-gravimetric (TG) analysis of SRF constituents was performed to understand the behaviour of fuel mixtures in the absence and presence of air. The results obtained from the experimental study will enhance the confidence of fuel users towards using MSW-derived SRF as an alternative fuel.

Wagland, S.T.; Kilgallon, P.; Coveney, R. [School of Applied Sciences, Sustainable Systems Department, Cranfield University, Cranfield, Bedfordshire MK43 0AL (United Kingdom); Garg, A. [Centre for Environmental Science and Engineering (CESE), Indian Institute of Technology Bombay, Powai, Mumbai 400076 (India); Smith, R.; Longhurst, P.J.; Pollard, S.J.T. [School of Applied Sciences, Sustainable Systems Department, Cranfield University, Cranfield, Bedfordshire MK43 0AL (United Kingdom); Simms, N., E-mail: n.j.simms@cranfield.ac.uk [School of Applied Sciences, Sustainable Systems Department, Cranfield University, Cranfield, Bedfordshire MK43 0AL (United Kingdom)

2011-06-15T23:59:59.000Z

168

Clean Coal Research | Department of Energy  

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

Clean Coal Research Clean Coal Research Clean Coal Turbines Gasification Fuel Cells Hydrogen from Coal Coal to Liquids Major Demonstrations Crosscutting Research Carbon Capture and...

169

Materials exposure test facilities for varying low-Btu coal-derived gas  

SciTech Connect

As a part of the United States Department of Energy's High Temperature Turbine Technology Readiness Program, the Morgantown Energy Technology Center is participating in the Ceramics Corrosion/Erosion Materials Study. The objective is to create a technology base for ceramic materials which could be used by stationary gas power turbines operating in a high-temperature, coal-derived, low-Btu gas products of combustion environment. Two METC facilities have been designed, fabricated and will be operated simultaneously exposing ceramic materials dynamically and statically to products of combustion of a coal-derived gas. The current studies will identify the degradation of ceramics due to their exposure to a coal-derived gas combustion environment.

Nakaishi, C.V.; Carpenter, L.K.

1980-01-01T23:59:59.000Z

170

Coal....  

U.S. Energy Information Administration (EIA)

Coal Prices and Earnings (updated August 12) According to Platts Coal Outlooks Weekly Price Survey (August 11), the ...

171

Coal....  

U.S. Energy Information Administration (EIA)

Coal Prices and Earnings (updated September 2) The average spot prices for coal traded last week were relatively ...

172

Method for improving the sedimentation and filterability of coal-derived liquids  

SciTech Connect

An improvement in the separation of suspended solids from coal-derived liquids by a separations process in which solids size is a separations parameter is achieved by contacting the coal-derived liquid containing suspended solids with an effective amount of an additive selected from the group of sulfuric acid, phosphoric acid, phosphoric anhydride and salts of sulfuric and phosphoric acid, and maintaining the contacted liquid at a temperature within the range of about 150.degree.-400.degree. C and for a time sufficient to achieve the desired separation rate.

Katz, Sidney (Oak Ridge, TN); Rodgers, Billy R. (Concord, TN)

1979-01-02T23:59:59.000Z

173

Coal liquefaction process streams characterization and evaluation: Analysis of coal-derived synthetic crude from HRI CTSL Run CC-15 and HRI Run CMSL-2  

SciTech Connect

Under subcontract from CONSOL Inc. (US DOE Contract No. DE-AC22-89PC89883), IIT Research Institute, National Institute for Petroleum and Energy Research applied a suite of petroleum inspection tests to two direct coal liquefactions net product oils produced in two direct coal liquefaction processing runs. Two technical reports, authored by NIPER, are presented here. The following assessment briefly describes the two coal liquefaction runs and highlights the major findings of the project. It generally is concluded that the methods used in these studies can help define the value of liquefaction products and the requirements for further processing. The application of these methods adds substantially to our understanding of the coal liquefaction process and the chemistry of coal-derived materials. These results will be incorporated by CONSOL into a general overview of the application of novel analytical techniques to coal-derived materials at the conclusion of this contract.

Sturm, G.P. Jr.; Kim, J.; Shay, J. [National Inst. for Petroleum and Energy Research, Bartlesville, OK (United States)

1994-01-01T23:59:59.000Z

174

Agenda for the Derived Liquids to Hydrogen Distributed Reforming Working Group (BILIWG) Hydrogen Production Technical Team Research Review  

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

& Hydrogen Production Technical Team Research Review Agenda for Tuesday, November 6, 2007 Location: BCS Incorporated, 8929 Stephens Road, Laurel, MD. 20723 410-997-7778 8:30 - 9:00 Continental Breakfast 9:00 DOE Targets, Tools and Technology o Bio-Derived Liquids to Hydrogen Distributed Reforming Targets DOE, Arlene Anderson o H2A Overview, NREL, Darlene Steward o Bio-Derived Liquids to Hydrogen Distributed Reforming Cost Analysis DTI, Brian James 10:00 Research Review o Low-Cost Hydrogen Distributed Production Systems, H2Gen, Sandy Thomas o Integrated Short Contact Time Hydrogen Generator, GE Global Research, Wei Wei o Distributed Bio-Oil Reforming, NREL, Darlene Steward o High Pressure Steam Ethanol Reforming, ANL, Romesh Kumar

175

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

DOE Green Energy (OSTI)

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2}S in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 130-156 seconds at 120-140 C to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases, evaluate removal capabilities of hydrogen sulfide and COS from coal gases with formulated catalysts, and develop an economic regeneration method of deactivated catalysts. Simulated coal gas mixtures consist of 3,300-3,800-ppmv hydrogen sulfide, 1,600-1,900 ppmv sulfur dioxide, 18-21 v% hydrogen, 29-34 v% CO, 8-10 v% CO{sub 2}, 5-18 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 114-132 SCCM. The temperature of the reactor is controlled in an oven at 120-140 C. The pressure of the reactor is maintained at 116-129 psia. The molar ratio of H{sub 2}S to SO{sub 2} in the monolithic catalyst reactor is

K. C. Kwon

2007-09-30T23:59:59.000Z

176

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

DOE Green Energy (OSTI)

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2}S in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash coat, and catalytic metals, to develop a regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor. The task of developing kinetic rate equations and modeling the direct oxidation process to assist in the design of large-scale plants will be abandoned since formulation of catalysts suitable for the removal of H{sub 2}S and COS is being in progress. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 46-570 seconds under reaction conditions to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases and evaluate their capabilities in reducing hydrogen sulfide and COS in coal gases. Simulated coal gas mixtures consist of 3,200-4,000-ppmv hydrogen sulfide, 1,600-20,000-ppmv sulfur dioxide, 18-27 v% hydrogen, 29-41 v% CO, 8-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of simulated coal gas mixtures to the reactor are 30 - 180 cm{sup 3}/min at 1 atm and 25 C (SCCM). The temperature of the reactor is controlled in an oven at 120-155 C. The pressure of the reactor is maintained at 40-210 psia. The molar ratio

K.C. Kwon

2009-09-30T23:59:59.000Z

177

Production of jet fuels from coal derived liquids  

SciTech Connect

Amoco and Lummus Crest have developed seven cases for upgrading by-product liquids from the Great Plains Coal Gasification Plant to jet fuels, and in several of the cases, saleable chemicals in addition to jet fuels. The analysis shows that the various grades of jet fuel can be produced from the Great Plains tar oil, but not economically. However, the phenolic and naphtha streams do have the potential to significantly increase (on the order of $10--15 million/year) the net revenues at Great Plains by producing chemicals, especially cresylic acid, cresol, and xylenol. The amount of these chemicals, which can be marketed, is a concern, but profits can be generated even when oxygenated chemical sales are limited to 10 percent of the US market. Another concern is that while commercial processes exist to extract phenolic mixtures, these processes have not been demonstrated with the Great Plains phenolic stream. 9 refs., 24 figs., 14 tabs.

Fleming, B.A.; Fox, J.D.; Furlong, M.W.; Masin, J.G.; Sault, L.P.; Tatterson, D.F. (Amoco Oil Co., Naperville, IL (USA). Research and Development Dept.); Fornoff, L.L.; Link, M.A.; Stahlnecker, E.; Torster, K. (Lummus Crest, Inc., Bloomfield, NJ (USA))

1988-09-01T23:59:59.000Z

178

Air extraction in gas turbines burning coal-derived gas  

SciTech Connect

In the first phase of this contracted research, a comprehensive investigation was performed. Principally, the effort was directed to identify the technical barriers which might exist in integrating the air-blown coal gasification process with a hot gas cleanup scheme and the state-of-the-art, US made, heavy-frame gas turbine. The guiding rule of the integration is to keep the compressor and the expander unchanged if possible. Because of the low-heat content of coal gas and of the need to accommodate air extraction, the combustor and perhaps, the flow region between the compressor exit and the expander inlet might need to be modified. In selecting a compressed air extraction scheme, one must consider how the scheme affects the air supply to the hot section of the turbine and the total pressure loss in the flow region. Air extraction must preserve effective cooling of the hot components, such as the transition pieces. It must also ensure proper air/fuel mixing in the combustor, hence the combustor exit pattern factor. The overall thermal efficiency of the power plant can be increased by minimizing the total pressure loss in the diffusers associated with the air extraction. Therefore, a study of airflow in the pre- and dump-diffusers with and without air extraction would provide information crucial to attaining high-thermal efficiency and to preventing hot spots. The research group at Clemson University suggested using a Griffith diffuser for the prediffuser and extracting air from the diffuser inlet. The present research establishes that the analytically identified problems in the impingement cooling flow are factual. This phase of the contracted research substantiates experimentally the advantage of using the Griffith diffuser with air extraction at the diffuser inlet.

Yang, Tah-teh; Agrawal, A.K.; Kapat, J.S.

1993-11-01T23:59:59.000Z

179

Process for stabilizing the viscosity characteristics of coal derived materials and the stabilized materials obtained thereby  

SciTech Connect

A process is disclosed for stabilizing the viscosity of coal derived materials such as an SRC product by adding up to 5.0% by weight of a light volatile phenolic viscosity repressor. The viscosity will remain stabilized for a period of time of up to 4 months.

Bronfenbrenner, James C. (Allentown, PA); Foster, Edward P. (Allentown, PA); Tewari, Krishna (Allentown, PA)

1985-01-01T23:59:59.000Z

180

Enthalpy measurement of coal-derived liquids. Combined quarterly technical progress reports, April-June 1979 and July-September 1979. [Effect of association  

DOE Green Energy (OSTI)

Enthalpy measurements on a coal-derived naphtha and middle distillate, both produced by the SRC-II process, were made using flow calorimetry. The accuracy of the measurements, as reported by Omid, was within +- 1% of the measured enthalpy differences, ..delta..H. Experimental data for the naphtha were obtained over a pressure range of 100-300 psia and temperatures from 148/sup 0/ to 456/sup 0/F. The middle distillate enthalpy measurements were made in the pressure and temperature ranges of 130 to 1000 psia, and 157/sup 0/ to 675/sup 0/F, respectively. The methods of prediction of enthalpy developed for petroleum fractions were unsatisfactory when applied to the above data. A negative bias was observed in the predicted enthalpy values for several of the coal-liquids. Based on these results, it was theorized that the high experimental enthalpy values for coal-liquids were due to an energy of association attributed, primarily, to hydrogen-bonding effects. The petroleum-fraction enthalpy correlations were then tested on the experimental data for pure compounds, both associating and non-associating. The predicted values compared very well with the experimental results for non-associating model compounds. However, for associating model compounds the predicted enthalpy values were considerably lower than their experimental data. This served to confirm the basic premise that the high experimental enthalpy values, for model compounds and coal liquids, were a direct consequence of an energy of association attributed, primarily, to hydrogen-bonding effects.

Kidnay, A.J.; Yesavage, V.F.

1979-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
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181

Fuel Cell Technologies Office: Bio-Derived Liquids to Hydrogen...  

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

by reforming bio-liquids such as sugars, ethanol, or bio-oils or through gasification or pyrolysis of biomass feedstocks. In the near term, distributed hydrogen production...

182

Fuel Cell Technologies Office: Bio-Derived Liquids to Hydrogen...  

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

on October 24, 2006 Review of Working Group Charter & DOE RD&D Targets for Hydrogen Production from Renewable Liquid Fuels, Arlene Anderson, DOE Fuel Cell Technologies...

183

Biomass-derived Hydrogen-evolution catalyst and electrode  

combination of biomass and earth-abundant metals has resulted in a durable catalyst for splitting water into oxygen and hydrogen, which can be used as ...

184

Low-pressure hydrocracking of coal-derived Fischer-Tropsch waxes to diesel  

Science Conference Proceedings (OSTI)

Coal-derived low-temperature Fischer-Tropsch (LTFT) wax was hydrocracked at pressures of 3.5-7.0 MPa using silica-alumina-supported sulfided NiW/NiMo and an unsulfided noble metal catalyst, modified with MoO{sub 3}. A low-pressure operation at 3.5 MPa produced a highly isomerized diesel, having low cloud points (from -12 to -28{sup o}C) combined with high cetane numbers (69-73). These properties together with the extremely low sulfur ({lt}5 ppm) and aromatic ({lt}0.5%) contents place coal/liquid (CTL) derived distillates as highly valuable blending components to achieve Eurograde diesel specifications. The upgrading of coal-based LTFT waxes through hydrocracking to high-quality diesel fuel blend components in combination with commercial-feasible coal-integrated gasification combined cycle (coal-IGCC) CO{sub 2} capture and storage schemes should make CTL technology more attractive. 28 refs., 7 figs., 8 tabs.

Dieter Leckel [Sasol Technology Research and Development, Sasolburg (South Africa). Fischer-Tropsch Refinery Catalysis

2007-06-15T23:59:59.000Z

185

Production of jet fuel from coal-derived liquids  

SciTech Connect

Amoco and Lummus-Crest, under a contract with the United States Department of Energy, are evaluating the process options and economics for upgrading the naphtha, crude phenols, and tar oil by-products from the Great Plains Coal Gasification Plant to jet fuels and other salable products. Analytical characterizations of these three by-products indicate the range of products that can be manufactured from each and potential problems which could be encountered during refining. These characterizations, along with limited experimental data and Amoco's proprietary process models, were used to design conceptual processing schemes for maximizing the production of Grades JP-4, JP-8, and high-density (JP-8X) jet fuels from the by-product liquids. Conceptual designs have been completed and a case for profitable production of JP-8 has been selected for experimental testing and preliminary design. Samples of JP-4, JP-8, and JP-8X aviation turbine fuels have been manufactured from the Great Plains tar oil. Larger samples of JP-8 have also been produced and shipped to the US Air Force for further testing. Lummus-Crest Inc. is now completing a preliminary process design for the profitable production of JP-8 and has made recommendations for a production run to produce larger quantities of JP-8. 2 figs., 3 tabs.

Furlong, M.W.; Fox, J.D.; Masin, J.G.

1989-01-01T23:59:59.000Z

186

Production of jet fuel from coal-derived liquids  

SciTech Connect

Amoco and Lummus-Crest, under a contract with the United States Department of Energy, are evaluating the process options and economics for upgrading the naphtha, crude phenols, and tar oil by-products from the Great Plains Coal Gasification Plant to jet fuels and other salable products. Analytical characterizations of these three by-products indicate the range of products that can be manufactured from each and potential problems which could be encountered during refining. These characterizations, along with limited experimental data and Amoco's proprietary process models, were used to design conceptual processing schemes for maximizing the production of Grades JP-4, JP-8, and high-density (JP-8X) jet fuels from the by-product liquids. Conceptual designs have been completed and a case for profitable production of JP-8 has been selected for experimental testing and preliminary design in the later phases of the contract. Samples of JP-4, JP-8, and JP-8X aviation turbine fuels have been manufactured from the Great Plains tar oil. Larger samples of JP-8 are nearly completed. Specification of a design basis for profitable production of JP-8 is under way. 5 figs., 4 tabs.

Furlong, M.W.; Fox, J.D.; Masin, J.G.

1988-01-01T23:59:59.000Z

187

Production of jet fuel from coal-derived liquids  

Science Conference Proceedings (OSTI)

Amoco and Lummus Crest, under a contract with the United States Department of Energy, are evaluating the process options and economics for upgrading the naphtha, crude phenols, and tar oil by-products from the Great Plains Coal Gasification Plant to jet fuels and other salable products. Conceptual processing schemes for maximizing the production of Grades JP-4, JP-8, and high-density (JP-8X) jet fuels, for maximizing profits, and for profitable production of each of the three jet fuels from the by-product liquids have been developed. Economic analyses of the designs show that jet fuel can be produced from the by-products, but not economically. However, jet fuel production could be subsidized profitably by processing the phenolic and naphtha streams to cresols, phenols, BTX, and other valuable chemical by-products. Uncertainties in the studies are marketability of the chemical by-products, replacement fuel costs, and viable schemes to process the phenol stream, among others. 8 figs., 2 tabs.

Furlong, M.W.; Fox, J.D.; Masin, J.G.; Soderberg, D.J.

1990-01-01T23:59:59.000Z

188

Production of jet fuels from coal derived liquids  

Science Conference Proceedings (OSTI)

Amoco Oil Company has conducted bench- and pilot plant-scale experiments to produce jet fuels from the tar oil from the Great Plains Coal Gasification Plant in Beulah, North Dakota. Experiments show that the hydroprocessing conditions recommended in Task 1 are not severe enough to saturate the aromatics in the tar oil to meet jet fuel specifications. Alternatives were investigated. Jet fuel specifications can be achieved when the tar oil is: hydrotreated in an expanded-bed hydrotreater to lower aromatics and heteroatom content; the effluent is then hydrotreated in a second, fixed bed hydrotreater; and, finally, the 550{degree}F boiling fraction from the two hydrotreaters is hydrocracked to extinction. The process was verified by pilot-plant production of 2 barrels of JP-8 turbine fuel, which met all but the flash point specification for JP-8. In addition, small samples of JP-4, JP-8, and high-density fuel were produced as a part of Task 2. 13 figs., 21 tabs.

Furlong, M.; Fox, J.; Masin, J.

1989-06-01T23:59:59.000Z

189

Production of jet fuel from coal-derived liquids  

SciTech Connect

Amoco and Lummus Crest, under a contract with the United States Department of Energy, are evaluating the process options and economics for upgrading the naphtha, crude phenols, and tar oil by-products from the Great Plains Coal Gasification Plant to jet fuels and other salable products. Analytical characterizations of these three by-products indicate the range of products that can be manufactured from each, and potential problems which could be encountered during refining. These characterizations, along with limited experimental data and Amoco's proprietary process models, were used to design conceptual processing schemes for maximizing the production of Grades JP-4, JP-8, and high-density (JP-8X) jet fuels from the by-product liquids. Conceptual designs have been completed and a case for profitable production of JP-8 has been selected for experimental testing and preliminary design in the later phases of the contract. Experimental work to date has shown that the tar oil stream requires substantially more severe processing than the preliminary design estimates indicated. A new design basis is now being tested and samples of JP-4, JP-8, and JP-8X are in production, based on that new, more severe processing scheme. Six barrels of tar oil have been hydrotreated according to the first step of the processing scheme and will be used to produce barrel quantities of JP-8. 2 refs., 2 figs.

Furlong, M.W.; Fox, J.D.; Masin, J.G.

1988-01-01T23:59:59.000Z

190

Production of jet fuel from coal-derived liquids  

Science Conference Proceedings (OSTI)

Amoco and Lummus Crest, under a contract with the United States Department of Energy, are evaluating the process options and economics for upgrading the naphtha, crude phenols, and tar oil by-products from the Great Plains Coal Gasification Plant to jet fuels and other salable products. Task 1 of the work, in which processes to produce each of the three jet fuels, JP-4, JP-8, and JP-8X, were designed, has been completed. The formal Task 1 report should issue next quarter. Task 2 work was initiated this quarter. In Task 2, process conditions for producing jet fuel from the Great Plains tar oil stream will be verified and samples of each of the three jet fuels will be produced. Experimental work shows that the hydrotreating conditions specified in Task 1 will not convert sufficient aromatics in the tar oil to produce jet fuel. Alternative schemes have been proposed and are being tested in the laboratories at Amoco Research Center. The simplest of these schemes, in which the heavy ends from the hydrotreater are recycled to extinction, was tested and proved infeasible. A second stage, fixed bed hydrotreater will be added to the process along with the expanded bed, first-stage hydrotreater and the hydrocracker specified in the Task 1 design. Future work will include additional experiments to specify the best process configuration and production of samples of each of the three grades of jet fuel. 6 figs., 7 tabs.

Furlong, M.W.; Fox, J.D.; Masin, J.G.; Soderberg, D.J.

1988-01-01T23:59:59.000Z

191

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

DOE Green Energy (OSTI)

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2} in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives using a monolithic catalyst reactor, experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 40-560 seconds at 120-150 C to evaluate effects of reaction temperatures, total pressure, space time, and catalyst regeneration on conversion of hydrogen sulfide into elemental sulfur and formation of COS. Simulated coal gas mixtures consist of 3,600-4,000-ppmv hydrogen sulfide, 1,800-2,000 ppmv sulfur dioxide, 23-27 v% hydrogen, 36-41 v% CO, 10-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 30-180 SCCM. The temperature of the reactor is controlled in an oven at 120-150 C. The pressure of the reactor is maintained at 40-210 psia. The molar ratio of H{sub 2}S to SO{sub 2} in the monolithic catalyst reactor is mai

K. C. Kwon

2006-09-30T23:59:59.000Z

192

Coal-firing sulfur coal with refuse derived fuels. Technical progress report {number_sign}7, [April--June 1996  

DOE Green Energy (OSTI)

The objectives for this quarter of study on the co-firing of high sulfur coal with refuse derived fuels project were two-fold. First, the organic compounds tentatively identified as combustion products in the previous report were confirmed by comparing retention times with pure samples. Secondly, a reduced amount of unburned carbon in the fly ash and an oxygen concentration at about 3--6% in the flue gases were achieved by the addition of removable heat exchange tubes in the AFBC system.

Pan, Wei-Ping, Riley, J.T.; Lloyd, W.G.

1996-05-31T23:59:59.000Z

193

Coal....  

U.S. Energy Information Administration (EIA)

DOE EIA WEEKLY COAL ... Coal Prices and Earnings (updated July 7, 2004) In the trading week ended July 2, the average spot coal prices tracked by EIA were mixed.

194

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

DOE Patents (OSTI)

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

Siriwardane, R.V.

1995-12-31T23:59:59.000Z

195

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

DOE Patents (OSTI)

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

Siriwardane, Ranjani V. (Morgantown, WV)

1997-01-01T23:59:59.000Z

196

Durable regenerable sorbent pellets for removal of hydrogen sulfide coal gas  

DOE Patents (OSTI)

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

Siriwardane, Ranjani V. (Morgantown, WV)

1999-01-01T23:59:59.000Z

197

Bio-Derived Liquids to Hydrogen Distributed Reforming Targets...  

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

Group includes individuals from DOE, the national laboratories, industry, and academia. Corn Stover Harvest Bio-Derived Liquids Reforming Distributed reforming of biomass derived...

198

Coal gasification apparatus  

DOE Patents (OSTI)

Coal hydrogenation vessel has hydrogen heating passages extending vertically through its wall and opening into its interior.

Nagy, Charles K. (Monaca, PA)

1982-01-01T23:59:59.000Z

199

Coal-oil slurry preparation  

DOE Patents (OSTI)

A pumpable slurry of pulverized coal in a coal-derived hydrocarbon oil carrier which slurry is useful as a low-ash, low-sulfur clean fuel, is produced from a high sulfur-containing coal. The initial pulverized coal is separated by gravity differentiation into (1) a high density refuse fraction containing the major portion of non-coal mineral products and sulfur, (2) a lowest density fraction of low sulfur content and (3) a middlings fraction of intermediate sulfur and ash content. The refuse fraction (1) is gasified by partial combustion producing a crude gas product from which a hydrogen stream is separated for use in hydrogenative liquefaction of the middlings fraction (3). The lowest density fraction (2) is mixed with the liquefied coal product to provide the desired fuel slurry. Preferably there is also separately recovered from the coal liquefaction LPG and pipeline gas.

Tao, John C. (Perkiomenville, PA)

1983-01-01T23:59:59.000Z

200

Analysis of the market and product costs for coal-derived high Btu gas  

Science Conference Proceedings (OSTI)

DOE analyzed the market potential and economics of coal-derived high-Btu gas using supply and demand projections that reflect the effects of natural gas deregulation, recent large oil-price rises, and new or pending legislation designed to reduce oil imports. The results indicate that an increasingly large market for supplemental gas should open up by 1990 and that SNG from advanced technology will probably be as cheap as gas imports over a wide range of assumptions. Although several studies suggest that a considerable market for intermediate-Btu gas will also exist, the potential supplemental gas demand is large enough to support both intermediate - and high-Btu gas from coal. Advanced SNG-production technology will be particularly important for processing the US's abundant, moderately to highly caking Eastern coals, which current technology cannot handle economically.

Not Available

1980-12-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

Emissions Resulting from the Full-Scale Cofiring of Pelletized Refuse-Derived Fuel and Coal  

E-Print Network (OSTI)

Full-scale cofiring tests of binder-enhanced pellets of densified, refuse-derived fuel (dRDF) and high-sulfur coal were conducted during June and July of 1987 in Boiler #5 at Argonne National Laboratory. These tests were conducted with industry, state, and municipality participation both in critiquing the test plan and in witnessing the actual test runs. Approximately 600 tons of dRDF containing 0%, 4%, or 8% binder were blended with high-sulfur coal at levels of up to 30%, based on the BTU content. This paper describes the dRDF/coal cofiring tests, the emissions and ash samples that were taken, the analyses that were conducted on these samples, preliminary test results, and future research plans.

Ohlsson, O. O.; Daugherty, K.; Venables, B.

1988-09-01T23:59:59.000Z

202

Seeking for ultrashort "non-bonded" hydrogen-hydrogen contacts in some rigid hydrocarbons and their derivatives  

E-Print Network (OSTI)

In this communication a systematic computational survey is done on some rigid hydrocarbon skeletons and their chlorinated derivatives in order to seek for the so-called ultrashort "non-bonded" hydrogen-hydrogen contacts. It is demonstrated that upon a proper choice of the main hydrocarbons backbone and adding some bulky chlorine atoms instead of the original hydrogen atoms in parts of the employed hydrocarbons, the resulting strain triggers structural changes that yields ultrashort hydrogen-hydrogen contacts with distances as small as 1.38 Angstrom. Such ultrashort contacts is clearly less than the world record of a ultrashort non-bonded hydrogen-hydrogen contact, 1.56 Angstrom, very recently realized experimentally by Pascal and coworkers in in,in-bis(hydrosilane) [J. Am. Chem. Soc. 135, 13235 (2013)]. Accordingly, it is demonstrated that various backbones, e.g. half-cage pentacyclododecanes and tetracyclododecanes, after proper structural modifications, are capable to reveal ultrashort non-bonded hydrogen-h...

Firouzi, Rohoullah

2013-01-01T23:59:59.000Z

203

Fuel Cell Technologies Office: Bio-Derived Liquids to Hydrogen Distributed  

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

Group Meeting - November 2007 Group Meeting - November 2007 The Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group participated in a Hydrogen Production Technical Team Research Review on November 6, 2007. The meeting provided the opportunity for researchers to share their experiences in converting bio-derived liquids to hydrogen with members of the Department of Energy Hydrogen Production Technical Team. The following meeting documents are available as Adobe Acrobat PDFs. Download Adobe Reader. Proceedings Agenda, discussion points, and participant list (PDF 146 KB) Action items and meeting highlights (PDF 104 KB) 2007 Annual Merit Review Report excerpts on bio-derived liquids to hydrogen distributed reforming research (PDF 3.9 MB) Presentations DOE Targets, Tools, and Technology

204

Integrated High Temperature Coal-to-Hydrogen System with CO2 Separation  

DOE Green Energy (OSTI)

A significant barrier to the commercialization of coal-to-hydrogen technologies is high capital cost. The purity requirements for H{sub 2} fuels are generally met by using a series of unit clean-up operations for residual CO removal, sulfur removal, CO{sub 2} removal and final gas polishing to achieve pure H{sub 2}. A substantial reduction in cost can be attained by reducing the number of process operations for H{sub 2} cleanup, and process efficiency can be increased by conducting syngas cleanup at higher temperatures. The objective of this program was to develop the scientific basis for a single high-temperature syngas-cleanup module to produce a pure stream of H{sub 2} from a coal-based system. The approach was to evaluate the feasibility of a 'one box' process that combines a shift reactor with a high-temperature CO{sub 2}-selective membrane to convert CO to CO{sub 2}, remove sulfur compounds, and remove CO{sub 2} in a simple, compact, fully integrated system. A system-level design was produced for a shift reactor that incorporates a high-temperature membrane. The membrane performance targets were determined. System level benefits were evaluated for a coal-to-hydrogen system that would incorporate membranes with properties that would meet the performance targets. The scientific basis for high temperature CO{sub 2}-selective membranes was evaluated by developing and validating a model for high temperature surface flow membranes. Synthesis approaches were pursued for producing membranes that integrated control of pore size with materials adsorption properties. Room temperature reverse-selectivity for CO{sub 2} was observed and performance at higher temperatures was evaluated. Implications for future membrane development are discussed.

James A. Ruud; Anthony Ku; Vidya Ramaswamy; Wei Wei; Patrick Willson

2007-05-31T23:59:59.000Z

205

Production and Optimization of Direct Coal Liquefaction derived Low Carbon-Footprint Transportation Fuels  

DOE Green Energy (OSTI)

This report summarizes works conducted under DOE Contract No. DE-FC26-05NT42448. The work scope was divided into two categories - (a) experimental program to pretreat and refine a coal derived syncrude sample to meet transportation fuels requirements; (b) system analysis of a commercial scale direct coal liquefaction facility. The coal syncrude was derived from a bituminous coal by Headwaters CTL, while the refining study was carried out under a subcontract to Axens North America. The system analysis included H{sub 2} production cost via six different options, conceptual process design, utilities requirements, CO{sub 2} emission and overall plant economy. As part of the system analysis, impact of various H{sub 2} production options was evaluated. For consistence the comparison was carried out using the DOE H2A model. However, assumptions in the model were updated using Headwaters database. Results of Tier 2 jet fuel specifications evaluation by the Fuels & Energy Branch, US Air Force Research Laboratory (AFRL/RZPF) located at Wright Patterson Air Force Base (Ohio) are also discussed in this report.

Steven Markovich

2010-06-30T23:59:59.000Z

206

Hydrogen and electricity from coal with carbon dioxide separation using chemical looping reactors  

SciTech Connect

Concern about global climate change has led to research on low CO{sub 2} emission in the process of the energy conversion of fossil fuel. One of the solutions is the conversion of fossil fuel into carbon-free energy carriers, hydrogen, and electricity with CO{sub 2} capture and storage. In this paper, the main purpose is to investigate the thermodynamics performance of converting coal to a hydrogen and electricity system with chemical-looping reactors and to explore the influences of operating parameters on the system performance. Using FeO/Fe{sub 3}O{sub 4} as an oxygen carrier, we propose a carbon-free coproduction system of hydrogen and electricity with chemical-looping reactors. The performance of the new system is simulated using ASPEN PLUS software tool. The influences of the chemical-looping reactor's temperature, steam conversion rate, and O{sub 2}/coal quality ratio on the system performance, and the exergy performance are discussed. The results show that a high-purity of H{sub 2} (99.9%) is reached and that CO{sub 2} can be separated. The system efficiency is 57.85% assuming steam reactor at 815 C and the steam conversion rate 37%. The system efficiency is affected by the steam conversion rate, rising from 53.17 to 58.33% with the increase of the steam conversion rate from 28 to 41%. The exergy efficiency is 54.25% and the losses are mainly in the process of gasification and HRSG. 14 refs., 12 figs., 3 tabs.

Xiang Wenguo; Chen Yingying [Southeast University, Nanjing (China). Key Laboratory of Clean Coal Power Generation and Combustion Technology of Ministry of Education

2007-08-15T23:59:59.000Z

207

www.elsevier.com/locate/fuel Trace elements in coal derived liquids: analysis by ICP-MS and  

E-Print Network (OSTI)

Concentrations of trace elements in coal derived liquids have been investigated by inductively coupled plasma-mass spectrometry (ICP-MS) and by Mssbauer spectroscopy. Liquefaction extracts prepared from the Argonne Premium Coals and a coal tar pitch have been examined. Microwave digestion in concentrated nitric acid has been shown as a suitable method for determining trace element concentrations in coal derived liquids by ICP-MSfor sample sizes as small as 320 mg. High concentrations of Fe were found for all extract samples (?2651474 ppm). Ti, Cr, Mn, Co, Ga, Sb, Cs and Ba were measurable. Concentration distributions of trace elements found in the extracts bore little relation to the corresponding distributions in the original coals. The proportions of individual trace elements present in the original coals and found in the extracts, varied widely. Mssbauer spectroscopy of the extracts indicated that the high Fe-concentrations corresponded to the presence of organometallic-Fe compoundsand not to pyritic iron. There is evidence suggesting the presence of material derived from iron-storage proteins such as ferritin, but final proof is lacking. Our data suggest that other metallic ions detected in these coal derived liquids may be present in association with the organic material. Concentrations of paramagnetic metal species were found to be of the same order of magnitude as ESR spin-densities already found in coal liquids. Both types of paramagnetic species are suspected of causing loss of signal in

Mssbauer Spectroscopy; R. Richaud A; H. Lachas A; M. -j. Lazaro A; L. J. Clarke B; K. E. Jarvis B; A. A. Herod A; T. C. Gibb C; R. Kandiyoti A

1999-01-01T23:59:59.000Z

208

Effects of coal-derived trace species on performance of molten carbonate fuel cells. Final report  

DOE Green Energy (OSTI)

The Carbonate Fuel Cell is a very promising option for highly efficient generation of electricity from many fuels. If coal-gas is to be used, the interactions of coal-derived impurities on various fuel cell components need to be understood. Thus the effects on Carbonate Fuel Cell performance due to ten different coal-derived contaminants viz., NH{sub 3}, H{sub 2}S, HC{ell}, H{sub 2}Se, AsH{sub 3}, Zn, Pb, Cd, Sn, and Hg, have been studied at Energy Research Corporation. Both experimental and theoretical evaluations were performed, which have led to mechanistic insights and initial estimation of qualitative tolerance levels for each species individually and in combination with other species. The focus of this study was to investigate possible coal-gas contaminant effects on the anode side of the Carbonate Fuel Cell, using both out-of-cell thermogravimetric analysis by isothermal TGA, and fuel cell testing in bench-scale cells. Separate experiments detailing performance decay in these cells with high levels of ammonia contamination (1 vol %) and with trace levels of Cd, Hg, and Sn, have indicated that, on the whole, these elements do not affect carbonate fuel cell performance. However, some performance decay may result when a number of the other six species are present, singly or simultaneously, as contaminants in fuel gas. In all cases, tolerance levels have been estimated for each of the 10 species and preliminary models have been developed for six of them. At this stage the models are limited to isothermal, benchscale (300 cm{sup 2} size) single cells. The information obtained is expected to assist in the development of coal-gas cleanup systems, while the contaminant performance effects data will provide useful basic information for modeling fuel cell endurance in conjunction with integrated gasifier/fuel-cell systems (IGFC).

Not Available

1992-05-01T23:59:59.000Z

209

Effects of coal-derived trace species on performance of molten carbonate fuel cells  

DOE Green Energy (OSTI)

The Carbonate Fuel Cell is a very promising option for highly efficient generation of electricity from many fuels. If coal-gas is to be used, the interactions of coal-derived impurities on various fuel cell components need to be understood. Thus the effects on Carbonate Fuel Cell performance due to ten different coal-derived contaminants viz., NH{sub 3}, H{sub 2}S, HC{ell}, H{sub 2}Se, AsH{sub 3}, Zn, Pb, Cd, Sn, and Hg, have been studied at Energy Research Corporation. Both experimental and theoretical evaluations were performed, which have led to mechanistic insights and initial estimation of qualitative tolerance levels for each species individually and in combination with other species. The focus of this study was to investigate possible coal-gas contaminant effects on the anode side of the Carbonate Fuel Cell, using both out-of-cell thermogravimetric analysis by isothermal TGA, and fuel cell testing in bench-scale cells. Separate experiments detailing performance decay in these cells with high levels of ammonia contamination (1 vol %) and with trace levels of Cd, Hg, and Sn, have indicated that, on the whole, these elements do not affect carbonate fuel cell performance. However, some performance decay may result when a number of the other six species are present, singly or simultaneously, as contaminants in fuel gas. In all cases, tolerance levels have been estimated for each of the 10 species and preliminary models have been developed for six of them. At this stage the models are limited to isothermal, benchscale (300 cm{sup 2} size) single cells. The information obtained is expected to assist in the development of coal-gas cleanup systems, while the contaminant performance effects data will provide useful basic information for modeling fuel cell endurance in conjunction with integrated gasifier/fuel-cell systems (IGFC).

Not Available

1992-05-01T23:59:59.000Z

210

COAL DERIVED MATRIX PITCHES FOR CARBON-CARBON COMPOSITE MANUFACTURE/PRODUCTION OF FIBERS AND COMPOSITES FROM COAL-BASED PRECURSORS  

Science Conference Proceedings (OSTI)

The Consortium for premium Carbon Products from Coal, with funding from the US Department of Energy, National Energy Technology Laboratory continue with the development of innovative technologies that will allow coal or coal-derived feedstocks to be used in the production of value-added carbon materials. In addition to supporting eleven independent projects during budget period 3, three meetings were held at two separate locations for the membership. The first was held at Nemacolin Woodlands Resort on May 15-16, 2000. This was followed by two meetings at Penn State, a tutorial on August 11, 2000 and a technical progress meeting on October 26-27.

Peter G. Stansberry; John W. Zondlo

2001-07-01T23:59:59.000Z

211

Refinery Integration of By-Products from Coal-Derived Jet Fuels  

SciTech Connect

The final report summarizes the accomplishments toward project goals during length of the project. The goal of this project was to integrate coal into a refinery in order to produce coal-based jet fuel, with the major goal to examine the products other than jet fuel. These products are in the gasoline, diesel and fuel oil range and result from coal-based jet fuel production from an Air Force funded program. The main goal of Task 1 was the production of coal-based jet fuel and other products that would need to be utilized in other fuels or for non-fuel sources, using known refining technology. The gasoline, diesel fuel, and fuel oil were tested in other aspects of the project. Light cycle oil (LCO) and refined chemical oil (RCO) were blended, hydrotreated to removed sulfur, and hydrogenated, then fractionated in the original production of jet fuel. Two main approaches, taken during the project period, varied where the fractionation took place, in order to preserve the life of catalysts used, which includes (1) fractionation of the hydrotreated blend to remove sulfur and nitrogen, followed by a hydrogenation step of the lighter fraction, and (2) fractionation of the LCO and RCO before any hydrotreatment. Task 2 involved assessment of the impact of refinery integration of JP-900 production on gasoline and diesel fuel. Fuel properties, ignition characteristics and engine combustion of model fuels and fuel samples from pilot-scale production runs were characterized. The model fuels used to represent the coal-based fuel streams were blended into full-boiling range fuels to simulate the mixing of fuel streams within the refinery to create potential 'finished' fuels. The representative compounds of the coal-based gasoline were cyclohexane and methyl cyclohexane, and for the coal-base diesel fuel they were fluorine and phenanthrene. Both the octane number (ON) of the coal-based gasoline and the cetane number (CN) of the coal-based diesel were low, relative to commercial fuels ({approx}60 ON for coal-based gasoline and {approx}20 CN for coal-based diesel fuel). Therefore, the allowable range of blending levels was studied where the blend would achieve acceptable performance. However, in both cases of the coal-based fuels, their ignition characteristics may make them ideal fuels for advanced combustion strategies where lower ON and CN are desirable. Task 3 was designed to develop new approaches for producing ultra clean fuels and value-added chemicals from refinery streams involving coal as a part of the feedstock. It consisted of the following three parts: (1) desulfurization and denitrogenation which involves both new adsorption approach for selective removal of nitrogen and sulfur and new catalysts for more effective hydrotreating and the combination of adsorption denitrogenation with hydrodesulfurization; (2) saturation of two-ring aromatics that included new design of sulfur resistant noble-metal catalysts for hydrogenation of naphthalene and tetralin in middle distillate fuels, and (3) value-added chemicals from naphthalene and biphenyl, which aimed at developing value-added organic chemicals from refinery streams such as 2,6-dimethylnaphthalene and 4,4{prime}-dimethylbiphenyl as precursors to advanced polymer materials. Major advances were achieved in this project in designing the catalysts and sorbent materials, and in developing fundamental understanding. The objective of Task 4 was to evaluate the effect of introducing coal into an existing petroleum refinery on the fuel oil product, specifically trace element emissions. Activities performed to accomplish this objective included analyzing two petroleum-based commercial heavy fuel oils (i.e., No. 6 fuel oils) as baseline fuels and three co-processed fuel oils, characterizing the atomization performance of a No. 6 fuel oil, measuring the combustion performance and emissions of the five fuels, specifically major, minor, and trace elements when fired in a watertube boiler designed for natural gas/fuel oil, and determining the boiler performance when firing the five fuels. Two

Caroline Clifford; Andre Boehman; Chunshan Song; Bruce Miller; Gareth Mitchell

2008-03-31T23:59:59.000Z

212

The mobile phase in coals: Its nature and modes of release: Final report: Part 1, Structural inferences from dry catalytic hydrogenation of a subbituminous coal  

DOE Green Energy (OSTI)

In a study to provide insight into the two component structural model of coal and the mechanisms of coal liquefaction, an approach was adopted in which a subbituminous coal was reacted with hydrogen in the presence of an impregnated molybdenum sulphide catalyst and in the absence of solvent. Reactions were conducted at temperatures between 300 and 400/sup 0/C and for reaction times up to 180 min. The composition and yields of gaseous products, chloroform-soluble liquids and insoluble residues were followed as a function of the reaction conditions by means of different analytical and characterization techniques: gas chromatography; /sup 1/H NMR; elemental analysis; FTIR; solvent swelling in pyridine. 105 refs., 20 figs., 12 tabs.

Terrer, M.T.; Derbyshire, F.J.

1986-12-01T23:59:59.000Z

213

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

214

Regenerable Sorbent Development for Sulfur, Chloride and Ammonia Removal from Coal-Derived Synthesis Gas  

DOE Green Energy (OSTI)

A large number of components in coal form corrosive and toxic compounds during coal gasification processes. DOEs NETL aims to reduce contaminants to parts per billion in order to utilize gasification gas streams in fuel cell applications. Even more stringent requirements are expected if the fuel is to be utilized in chemical production applications. Regenerable hydrogen sulfide removal sorbents have been developed at NETL. These sorbents can remove the hydrogen sulfide to ppb range at 316 C and at 20 atmospheres. The sorbent can be regenerated with oxygen. Reactivity and physical durability of the sorbent did not change during the multi-cycle tests. The sorbent development work has been extended to include the removal of other major impurities, such as HCl and NH3. The sorbents for HCl removal that are available today are not regenerable. Regenerable HCl removal sorbents have been developed at NETL. These sorbents can remove HCl to ppb range at 300 C to 500 C. The sorbent can be regenerated with oxygen. Results of TGA and bench-scale flow reactor tests with both regenerable and non-regenerable HCl removal sorbents will be discussed in the paper. Bench-scale reactor tests were also conducted with NH3 removal sorbents. The results indicated that the sorbents have a high removal capacity and good regenerability during the multi-cycle tests. Future emphasis of the NETL coal gasification/cleanup program is to develop multi-functional sorbents to remove multiple impurities in order to minimize the steps involved in the cleanup systems. To accomplish this goal, a regenerable sorbent capable of removing both HCl and H2S was developed. The results of the TGA conducted with the sorbent to evaluate the feasibility of both H2S and HCl sorption will be discussed in this paper.

Siriwardane, R.V.; Tian, H.; Simonyi, T.; Webster, T.

2007-08-01T23:59:59.000Z

215

Photoelectrochemical Hydrogen Production Using New Combinatorial Chemistry Derived Materials  

DOE Green Energy (OSTI)

Solar photoelectrochemical water-splitting has long been viewed as one of the holy grails of chemistry because of its potential impact as a clean, renewable method of fuel production. Several known photocatalytic semiconductors can be used; however, the fundamental mechanisms of the process remain poorly understood and no known material has the required properties for cost effective hydrogen production. In order to investigate morphological and compositional variations in metal oxides as they relate to opto-electrochemical properties, we have employed a combinatorial methodology using automated, high-throughput, electrochemical synthesis and screening together with conventional solid-state methods. This report discusses a number of novel, high-throughput instruments developed during this project for the expeditious discovery of improved materials for photoelectrochemical hydrogen production. Also described within this report are results from a variety of materials (primarily tungsten oxide, zinc oxide, molybdenum oxide, copper oxide and titanium dioxide) whose properties were modified and improved by either layering, inter-mixing, or doping with one or more transition metals. Furthermore, the morphologies of certain materials were also modified through the use of structure directing agents (SDA) during synthesis to create mesostructures (features 2-50 nm) that increased surface area and improved rates of hydrogen production.

Jaramillo, Thomas F.; Baeck, Sung-Hyeon; Kleiman-Shwarsctein, Alan; Stucky, Galen D. (PI); McFarland, Eric W. (PI)

2004-10-25T23:59:59.000Z

216

DESULFURIZATION OF COAL MODEL COMPOUNDS AND COAL LIQUIDS  

E-Print Network (OSTI)

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

Wrathall, James Anthony

2011-01-01T23:59:59.000Z

217

Investigation of the filtration processes of coal hydrogenation slurries and suspensions obtained after the extraction of oils  

Science Conference Proceedings (OSTI)

As a result of an investigation of the filtration of slurries and their suspensions in hydrogenates under a pressure difference ..delta..P = 0.03 MPa at t = 25 to 120/sup 8/C on various filtration barriers (the ash content of the filtrates did not exceed 0.1%) it was established that the filtration rate of the slurries and their suspensions in hydrogenates is strongly dependent on the type of coal and the hydrogenation conditions and decreases as the content of solid substances and asphaltenes increases. The rate of filtration of the suspensions of the slurries in the hydrogenates is approximately an order of magnitude greater than that of the original slurries; this is due to the sharp drop in the viscosity of the liquid and the aggregation of the small solid particles when the slurry is mixed with the hydrogenate. The rate of filtration for the slurries can be increased by adding auxiliary substances.

Gel'perin, N.I.; Pebalk, V.L.; Shashkova, M.N.; Gorlov, E.G.; Zotova, O.V.

1987-10-10T23:59:59.000Z

218

Prebaked Anode from Coal Extract  

Science Conference Proceedings (OSTI)

We previously reported that the coal extract prepared from non-hydrogenative extraction of thermal coals using two-ring-aromatic solvent (Hyper-coal) is suitable...

219

Co-firing high sulfur coal with refuse derived fuels. Quarterly report, October - December 1996  

DOE Green Energy (OSTI)

The objectives of this quarter of study on the co-firing of high sulfur coal with refuse derived fuels project were two-fold. First, the effect of S0{sub 2} on the formation of chlorine during combustion processes was examined. To simulate the conditions used in the AFBC system, experiments were conducted in a quartz tube in an electrically heated furnace. The principle analytical technique used for identification of the products from this study was GC/MS. The evolved gas was trapped by an absorbent and analyzed with a GC/MS system. The preliminary results indicate an inhibiting effect of S0{sub 2} on the Deacon Reaction. Secondly, information on the evolution of chlorine, sulfur and organic compounds from coals 95031 and 95011 were studied with the AFBC system. 2 figs., 1 tab.

Pan, W.-P.; Riley, J.T.; Lloyd, W.G.

1996-12-01T23:59:59.000Z

220

Process for coal liquefaction employing selective coal feed  

DOE Patents (OSTI)

An improved coal liquefaction process is provided whereby coal conversion is improved and yields of pentane soluble liquefaction products are increased. In this process, selected feed coal is pulverized and slurried with a process derived solvent, passed through a preheater and one or more dissolvers in the presence of hydrogen-rich gases at elevated temperatures and pressures, following which solids, including mineral ash and unconverted coal macerals, are separated from the condensed reactor effluent. The selected feed coals comprise washed coals having a substantial amount of mineral matter, preferably from about 25-75%, by weight, based upon run-of-mine coal, removed with at least 1.0% by weight of pyritic sulfur remaining and exhibiting vitrinite reflectance of less than about 0.70%.

Hoover, David S. (New Tripoli, PA); Givens, Edwin N. (Bethlehem, PA)

1983-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

Hydrogen recovery by novel solvent systems  

DOE Green Energy (OSTI)

The objective of this work is to develop a novel method for purification of hydrogen from coal-derived synthesis gas. The study involved a search for suitable mixtures of solvents for their ability to separate hydrogen from the coal derived gas stream in significant concentration near their critical point of miscibility. The properties of solvent pairs identified were investigated in more detail to provide data necessary for economic evaluation and process development.

Shinnar, R.; Ludmer, Z.; Ullmann, A.

1991-08-01T23:59:59.000Z

222

Chemically authentic surrogate mixture model for the thermophysical properties of a coal-derived liquid fuel  

Science Conference Proceedings (OSTI)

We developed a surrogate mixture model to represent the physical properties of a coal-derived liquid fuel using only information obtained from a gas chromatography-mass spectrometry analysis of the fuel and a recently developed 'advanced distillation curve'. We then predicted the density, speed of sound, and viscosity of the fuel and compared them to limited experimental data. The surrogate contains five components (n-propylcyclohexane, trans-decalin, {alpha}-methyldecalin, bicyclohexane, and n-hexadecane), yet comparisons to limited experimental data demonstrate that the model is able to represent the density, sound speed, and viscosity to within 1, 4, and 5%, respectively. 102 refs., 2 figs., 5 tabs.

M.L. Huber; E.W. Lemmon; V. Diky; B.L. Smith; T.J. Bruno [National Institute of Standards and Technology (NIST), Boulder, CO (United States). Physical and Chemical Properties Division

2008-09-15T23:59:59.000Z

223

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

224

Coal gasification apparatus. [Patent application  

DOE Patents (OSTI)

Coal hydrogenation vessel has hydrogen heating passages extending vertically through its wall and opening into its interior.

Nagy, C.K.

1981-04-24T23:59:59.000Z

225

Solids precipitation and polymerization of asphaltenes in coal-derived liquids  

DOE Patents (OSTI)

The precipitation and removal of particulate solids from coal-derived liquids by adding a process-derived anti-solvent liquid fraction and continuing the precipitation process at a temperature above the melting point of the mixed liquids for sufficient time to allow the asphaltenes to polymerize and solids to settle at atmospheric pressure conditions. The resulting clarified light hydrocarbon overflow liquid contains less than about 0.02 W % ash and is suitable as turbine fuel or as boiler fuel for burning without particulate emission control equipment. An underflow liquid fraction containing less than about 0.1 W % solids along with low sulfur and nitrogen concentrations is suitable as a boiler fuel with emission control equipment.

Kydd, Paul H. (Lawrenceville, NJ)

1984-01-01T23:59:59.000Z

226

NETL: Coal & Coal Biomass to Liquids - Systems Studies  

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

security and a sustainable hydrogen economy by economically producing hydrogen from coal. Hydrogen represents a clean alternative fuel that can help to reduce the nation's...

227

Synthesis of methyl methacrylate from coal-derived syngas: Quarterly report,, October 1-December 31, 1997  

SciTech Connect

Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of three steps of synthesis of a propionate, its condensation with formaldehyde, and esterification of resulting methacrylic acid (MAA) with methanol to produce MMA. Over the last quarter, Eastman developed two new processes which have resulted in two new invention reports. One process deals with carbonylation of benzyl ether which represents a model for coal liquefaction and the second focuses on the acceleration of carbonylation rates for propionic acid synthesis, via use of polar aprotic solvents. These two inventions are major improvements in the novel Mo-catalyzed homogeneous process for propionic acid synthesis technology, developed by Eastman. Over the last quarter, RTI completed three reaction cycles and two regeneration cycles as a part of long-term reaction regeneration cycle study on a 10% Nb{sub 2}O{sub 5}/Si0{sub 2} catalyst, for vapor phase condensation reaction of formaldehyde with propionic acid.

NONE

1998-09-01T23:59:59.000Z

228

Prediction of thermodynamic properties of coal derivatives. Final technical report, September 1, 1987--February 28, 1991  

Science Conference Proceedings (OSTI)

The purpose of this research program is to understand the relationship between macroscopic thermodynamic properties and the various types of intermolecular forces. Since coal-derived liquids contain a wide variety of compounds, a theory capable of successfully predicting the thermophysical properties for coal processes must take into account the molecular shapes and all significant intermolecular forces: dispersion forces, anisotropic forces due to dipoles and quadrupoles, as well as Lewis acid-base interactions. We have developed the Acid-Base-Perturbed-Anisotropic-Chain Theory (ABPACT), a comprehensive theory that is capable of predicting the thermophysical properties for many systems where these different intermolecular forces are present. The ABPACT can treat non-polar compounds, polar compounds and compounds that associate through Lewis acid-base interactions. In addition to our theoretical work, we have used computer simulations to evaluate (and in some cases correct) the assumptions made in this theory. We also have conducted experiments to help us better understand the interplay of different kinds of interactions in multicomponent mixtures.

Donohue, M.D.

1990-09-01T23:59:59.000Z

229

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

230

DOE Hydrogen Analysis Repository: Centralized Hydrogen Production...  

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

Coal Gasification with Sequestration Project Summary Full Title: Well-to-Wheels Case Study: Centralized Hydrogen Production from Coal Gasification with Sequestration Project ID:...

231

Carbide-Derived Carbons with Tunable Porosity Optimized for Hydrogen Storage  

Science Conference Proceedings (OSTI)

On-board hydrogen storage is a key requirement for fuel cell-powered cars and trucks. Porous carbon-based materials can in principle adsorb more hydrogen per unit weight at room temperature than liquid hydrogen at -176 oC. Achieving this goal requires interconnected pores with very high internal surface area, and binding energies between hydrogen and carbon significantly enhanced relative to H2 on graphite. In this project a systematic study of carbide-derived carbons, a novel form of porous carbon, was carried out to discover a high-performance hydrogen sorption material to meet the goal. In the event we were unable to improve on the state of the art in terms of stored hydrogen per unit weight, having encountered the same fundamental limit of all porous carbons: the very weak interaction between H2 and the carbon surface. On the other hand we did discover several strategies to improve storage capacity on a volume basis, which should be applicable to other forms of porous carbon. Further discoveries with potentially broader impacts include Proof that storage performance is not directly related to pore surface area, as had been previously claimed. Small pores (supercapacitors with record high specific capacitance, and perm-selective membranes which bind cytokines for control of infections and possibly hemodialysis filters.

Fisher, John E.; Gogotsi, Yury; Yildirim, Taner

2010-01-07T23:59:59.000Z

232

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

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

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

233

The Performance of Planar Solid Oxide Fuel Cells using Hydrogen-depleted Coal Syngas.  

E-Print Network (OSTI)

??Since solid oxide fuel cells can operate on fuel containing both hydrogen and carbon monoxide, it may prove possible to remove hydrogen from syngas streams (more)

Burnette, David D.

2007-01-01T23:59:59.000Z

234

Kinetics of catalyzed steam gasification of low-rank coals to produce hydrogen. Final report for the period ending March 31, 1986  

SciTech Connect

The principal goal of coal char-steam gasification research at the University of North Dakota Energy Research Center (UNDERC) is to establish the feasibility of low-rank coal gasification for hydrogen production. The program has focused on determining reaction conditions for maximum product gas hydrogen content and on evaluating process kinetics with and without catalyst addition. The high inherent reactivity of lignites and subbituminous coals, compared to coals of higher rank, make them the probable choice for use in steam gasification. An extensive matrix of char-steam gasification tests was performed in a laboratory-scale thermogravimetric analyzer (TGA) at temperatures of 700/sup 0/, 750/sup 0/, and 800/sup 0/C. Four low-rank coals and one bituminous coal were included in the TGA test matrix. Catalysts screened in the study included K/sub 2/CO/sub 3/, Na/sub 2/CO/sub 3/, trona, nahcolite, sunflower hull ash, and lignite ash. Results showed uncatalyzed North Dakota and Texas lignites to be slightly more reactive than a Wyoming subbituminous coal, and 8 to 10 times more reactive than an Illinois bituminous coal. Several catalysts that substantially improved low-rank coal steam gasification rates included pure and mineral (trona and nahcolite) alkali carbonates. The reactivity observed when using trona and nahcolite to catalyze the steam gasification was the highest, at nearly 3.5 times that without catalysts. The use of these inexpensive, naturally-occurring alkalis as gasification catalysts may result in elimination of the need for catalyst recovery in the hydrogen-from-coal process, thereby simplifying operation and improving process economics. The study included evaluations of temperature and catalyst loading effects, coal and catalyst screening, and determinations of the apparent activation energies of the steam gasification reaction. 11 refs., 23 figs., 9 tabs.

Galegher, S.J.; Timpe, R.C.; Willson, W.G.; Farnum, S.A.

1986-06-01T23:59:59.000Z

235

Infrastructure Costs Associated with Central Hydrogen Production from Biomass and Coal - DOE Hydrogen and Fuel Cells Program FY 2012 Annual Progress Report  

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

7 7 FY 2012 Annual Progress Report DOE Hydrogen and Fuel Cells Program Darlene Steward (Primary Contact), Billy Roberts, Karen Webster National Renewable Energy Laboratory (NREL) 15013 Denver West Parkway Golden, CO 80401-3305 Phone: (303) 275-3837 Email: Darlene.Steward@nrel.gov DOE Manager HQ: Fred Joseck Phone: (202) 586-7932 Email: Fred.Joseck@hq.doe.gov Project Start Date: Fiscal Year (FY) 2010 Project End Date: Project continuation and direction determined annually by DOE FY 2012 Objectives Elucidate the location-dependent variability of * infrastructure costs for biomass- and coal-based central hydrogen production and delivery and the tradeoffs inherent in plant-location choices Provide modeling output and correlations for use in other * integrated analyses and tools

236

Prediction of thermodynamic properties of coal derivatives. Final technical report, March 1, 1991--February 28, 1994  

Science Conference Proceedings (OSTI)

We have developed new equations of state for pure-component chain molecules. The excellent performance of complicated theories, such as the Generalized Flory Dimer (GFD) theory can be mimicked by simpler equations, if assumptions for the shape parameters are made. We developed engineering correlations based on GFD theory, using local composition theory to take into account attractive forces. During this period, we compared methods for calculating repulsive and attractive contributions to equation of state against computer simulation data for hard and square-well chains, and against experimental data from the literature. We also have studied microstructure and local order in fluids that contain asymmetric molecules. We developed a thermodynamic model for polar compounds based on a site-site interaction approach. We have shown the equivalence of various classes of theories for hydrogen bonding, and used this equivalence to derive a multiple site model for water. In addition, simple cubic equations of state have been applied to calculate physical and chemical-reaction equilibria in nonideal systems. We measured infinite dilution activity coefficients using HPLC. We also measured high pressure vapor liquid equilibria of ternary and quaternary systems containing supercritical solvents. We used FT-IR spectroscopy to examine self-association of aliphatic alcohols due to hydrogen bonding, and to investigate the hydrogen bonding in polymer-solvent mixtures.

Donohue, M.D.

1993-09-01T23:59:59.000Z

237

The evaluation of a coal-derived liquid as a feedstock for the production of high-density aviation turbine fuel  

DOE Green Energy (OSTI)

The conversion of coal-derived liquids to transportation fuels has been the subject of many studies sponsored by the US Department of Energy and the US Department of Defense. For the most part, these studies evaluated conventional petroleum processes for the production of specification-grade fuels. Recently, however, the interest of these two departments expanded to include the evaluation of alternate fossil fuels as a feedstock for the production of high-density aviation turbine fuel. In this study, we evaluated five processes for their ability to produce intermediates from a coal-derived liquid for the production of high-density turbine fuel. These processes include acid-base extraction to reduce the heteroatom content of the middle distillate and the atmospheric and vacuum gas oils, solvent dewaxing to reduce the paraffin (alkane) content of the atmospheric and vacuum gas oils, Attapulgus clay treatment to reduce the heteroatom content of the middle distillate, coking to reduce the distillate range of the vacuum gas oil, and hydrogenation to remove heteroatoms and to saturate aromatic rings in the middle distillate and atmospheric gas oil. The chemical and physical properties that the US Air Force considers critical for the development of high-denisty aviation turbine fuel are specific gravity and net heat of combustion. The target minimum values for these properties are a specific gravity of at least 0.85 and a net heat of combustion of at least 130,000 Btu/gal. In addition, the minimum hydrogen content is 13.0 wt %, the maximum freeze point is {minus}53{degrees}F ({minus}47{degrees}C), the maximum amount of aromatics is about 25 to 30 vol %, and the maximum amount of paraffins is 10 vol %. 13 refs., 20 tabs.

Thomas, K.P.; Hunter, D.E.

1989-08-01T23:59:59.000Z

238

Evaluation of sorbents for the cleanup of coal-derived synthesis gas at elevated temperatures  

E-Print Network (OSTI)

Integrated Gasification Combined Cycle (IGCC) with carbon dioxide capture is a promising technology to produce electricity from coal at a higher efficiency than with traditional subcritical pulverized coal (PC) power plants. ...

Couling, David Joseph

2012-01-01T23:59:59.000Z

239

Evaluation of coal pretreatment prior to co-processing  

SciTech Connect

The Western Research Institute is currently developing a mild gasification process for the recovery of a stabilized char product for use as a fuel. A liquid product of limited value is produced during the mild gasification process that may be suited as a co-processing vehicle for coal-oil co-processing. Research was conducted to evaluate co-processing of this mild gasification liquid with coal. The two major areas of research discussed in this report are: (1) coal pretreatment with a coal-derived liquid to induce coal swelling and promote catalyst dispersion and (2) co-processing coal that has been thermally pretreated in the presence of the mild gasification liquid. The results of the investigation to evaluate co-processing of coal that has been thermally pretreated in the presence of the mild gasification liquid indicate that the thermal pretreatment adversely affected the coal-oil co-processing under hydrogen pressure. Thermally pretreated coals co-processed under a hydrogen atmosphere and without benefit of catalyst exhibited about 86 wt % conversion as compared to 96 wt % for coal that was only thermally dried. The addition of the iron pentacarbonyl catalyst precursor to the thermally pretreated coals did improve the conversion to near that of the dried coal. Results from analysis of the product obtained from co-processing the Illinois No. 6 coal showed it was upgraded in terms of oxygen content and hydrogen to carbon atomic ratio when compared to the mild gasification liquid.

Guffey, F.D.; Barbour, F.A.; Blake, R.F.

1991-12-01T23:59:59.000Z

240

Carbide-Derived Carbons with Tunable Porosity Optimized for Hydrogen Storage  

SciTech Connect

On-board hydrogen storage is a key requirement for fuel cell-powered cars and trucks. Porous carbon-based materials can in principle adsorb more hydrogen per unit weight at room temperature than liquid hydrogen at -176 oC. Achieving this goal requires interconnected pores with very high internal surface area, and binding energies between hydrogen and carbon significantly enhanced relative to H2 on graphite. In this project a systematic study of carbide-derived carbons, a novel form of porous carbon, was carried out to discover a high-performance hydrogen sorption material to meet the goal. In the event we were unable to improve on the state of the art in terms of stored hydrogen per unit weight, having encountered the same fundamental limit of all porous carbons: the very weak interaction between H2 and the carbon surface. On the other hand we did discover several strategies to improve storage capacity on a volume basis, which should be applicable to other forms of porous carbon. Further discoveries with potentially broader impacts include Proof that storage performance is not directly related to pore surface area, as had been previously claimed. Small pores (< 1.5 nm) are much more effective in storing hydrogen than larger ones, such that many materials with large total surface areas are sub-par performers. Established that the distribution of pore sizes can be controlled during CDC synthesis, which opens the possibility of developing high performance materials within a common family while targeting widely disparate applications. Examples being actively pursued with other funding sources include methane storage, electrode materials for batteries and supercapacitors with record high specific capacitance, and perm-selective membranes which bind cytokines for control of infections and possibly hemodialysis filters.

Fisher, John E.; Gogotsi, Yury; Yildirim, Taner

2010-01-07T23:59:59.000Z

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241

Hydrogen recovery by novel solvent systems. Final report  

DOE Green Energy (OSTI)

The objective of this work is to develop a novel method for purification of hydrogen from coal-derived synthesis gas. The study involved a search for suitable mixtures of solvents for their ability to separate hydrogen from the coal derived gas stream in significant concentration near their critical point of miscibility. The properties of solvent pairs identified were investigated in more detail to provide data necessary for economic evaluation and process development.

Shinnar, R.; Ludmer, Z.; Ullmann, A.

1991-08-01T23:59:59.000Z

242

Refinery Integration of By-Products from Coal-Derived Jet Fuels  

Science Conference Proceedings (OSTI)

This report summarizes the accomplishments toward project goals during the first twelve months of the project to assess the properties and performance of coal based products. These products are in the gasoline, diesel and fuel oil range and result from coal based jet fuel production from an Air Force funded program. Specific areas of progress include generation of coal based material that has been fractionated into the desired refinery cuts, acquisition and installation of a research gasoline engine, and modification of diesel engines for use in evaluating diesel produced in the project. The desulfurization of sulfur containing components of coal and petroleum is being studied so that effective conversion of blended coal and petroleum streams can be efficiently converted to useful refinery products. Equipment is now in place to begin fuel oil evaluations to assess the quality of coal based fuel oil. Coal samples have procured and are being assessed for cleaning prior to use in coking studies.

Leslie R. Rudnick; Andre Boehman; Chunshan Song; Bruce Miller; John Andresen

2004-09-17T23:59:59.000Z

243

REFINERY INTEGRATION OF BY-PRODUCTS FROM COAL-DERIVED JET FUELS  

Science Conference Proceedings (OSTI)

This report summarizes the accomplishments toward project goals during the first six months of the project to assess the properties and performance of coal based products. These products are in the gasoline, diesel and fuel oil range and result from coal based jet fuel production from an Air Force funded program. Specific areas of progress include generation of coal based material that has been fractionated into the desired refinery cuts, acquisition and installation of a research gasoline engine, and modification of diesel engines for use in evaluating diesel produced in the project. The desulfurization of sulfur containing components of coal and petroleum is being studied so that effective conversion of blended coal and petroleum streams can be efficiently converted to useful refinery products. Equipment is now in place to begin fuel oil evaluations to assess the quality of coal based fuel oil. Coal samples have procured and are being assessed for cleaning prior to use in coking studies.

Leslie R. Rudnick; Andre Boehman; Chunshan Song; Bruce Miller; John Andresen

2004-04-23T23:59:59.000Z

244

REFINERY INTEGRATION OF BY-PRODUCTS FROM COAL-DERIVED JET FUELS  

SciTech Connect

This report summarizes the accomplishments toward project goals during the first six months of the second year of the project to assess the properties and performance of coal based products. These products are in the gasoline, diesel and fuel oil range and result from coal based jet fuel production from an Air Force funded program. Specific areas of progress include generation of coal based material that has been fractionated into the desired refinery cuts, acquisition and installation of a research gasoline engine, and modification of diesel engines for use in evaluating diesel produced in the project. The desulfurization of sulfur containing components of coal and petroleum is being studied so that effective conversion of blended coal and petroleum streams can be efficiently converted to useful refinery products. Equipment is now in place to begin fuel oil evaluations to assess the quality of coal based fuel oil. Coal samples have procured and are being assessed for cleaning prior to use in coking studies.

Leslie R. Rudnick; Andre Boehman; Chunshan Song; Bruce Miller; Gareth Mitchell

2005-05-18T23:59:59.000Z

245

Refinery Integration of By-Products from Coal-Derived Jet Fuels  

Science Conference Proceedings (OSTI)

This report summarizes the accomplishments toward project goals during the first six months of the second year of the project to assess the properties and performance of coal based products. These products are in the gasoline, diesel and fuel oil range and result from coal based jet fuel production from an Air Force funded program. Specific areas of progress include generation of coal based material that has been fractionated into the desired refinery cuts, acquisition and installation of a research gasoline engine, and modification of diesel engines for use in evaluating diesel produced in the project. The desulfurization of sulfur containing components of coal and petroleum is being studied so that effective conversion of blended coal and petroleum streams can be efficiently converted to useful refinery products. Evaluations to assess the quality of coal based fuel oil are reported. Coal samples have procured and are being assessed for cleaning prior to use in coking studies.

Leslie R. Rudnick; Andre Boehman; Chunshan Song; Bruce Miller; Gareth Mitchell

2005-11-17T23:59:59.000Z

246

Coal liquefaction in an inorganic-organic medium  

SciTech Connect

Improved process for liquefaction of coal by contacting pulverized coal in an inorganic-organic medium solvent system containing a ZnCl.sub.2 catalyst, a polar solvent with the structure RX where X is one of the elements O, N, S or P, and R is hydrogen or a lower hydrocarbon radical; the solvent system can contain a hydrogen donor solvent (and must when RX is water) which is immiscible in the ZnCl.sub.2 and is a hydroaromatic hydrocarbon, selected from tetralin, dihydrophenanthrene, dihydroanthracene or a hydrogenated coal derived hydroaromatic hydrocarbon distillate fraction.

Vermeulen, Theodore (Berkeley, CA); Grens, II, Edward A. (Danville, CA); Holten, Ronald R. (El Cerrito, CA)

1982-01-01T23:59:59.000Z

247

Integrated Warm Gas Multicontaminant Cleanup Technologies for Coal-Derived Syngas  

SciTech Connect

One of the key obstacles for the introduction of commercial gasification technology for the production of power with Integrated Gasification Combined Cycle (IGCC) plants or the production of value added chemicals, transportation fuels, and hydrogen has been the cost of these systems. This situation is particularly challenging because the United States has ample coal resources available as raw materials and effective use of these raw materials could help us meet our energy and transportation fuel needs while significantly reducing our need to import oil. One component of the cost of these systems that faces strong challenges for continuous improvement is removing the undesirable components present in the syngas. The need to limit the increase in cost of electricity to < 35% for new coal-based power plants which include CO{sub 2} capture and sequestration addresses both the growing social concern for global climate change resulting from the emission of greenhouse gas and in particular CO{sub 2} and the need to control cost increases to power production necessary to meet this social objective. Similar improvements to technologies for trace contaminants are getting similar pressure to reduce environmental emissions and reduce production costs for the syngas to enable production of chemicals from coal that is cost competitive with oil and natural gas. RTI, with DOE/NETL support, has been developing sorbent technologies that enable capture of trace contaminants and CO{sub 2} at temperatures above 400 °F that achieve better capture performance, lower costs and higher thermal efficiency. This report describes the specific work of sorbent development for mercury (Hg), arsenic (As), selenium (Se), cadmium (Cd), and phosphorous (P) and CO{sub 2} removal. Because the typical concentrations of Hg, As, Se, Cd, and P are less than 10 ppmv, the focus has been on single-use sorbents with sufficient capacity to ensure replacement costs are cost effective. The research in this report describes the development efforts which expand this sorbent development effort to include Se, Cd, and P as well as Hg and As. Additional research has focused on improving removal performance with the goal of achieving effluent concentrations that are suitable for chemical production applications. By contrast, sorbent development for CO{sub 2} capture has focused on regenerable sorbents that capture the CO{sub 2} byproduct at higher CO{sub 2} pressures. Previous research on CO{sub 2} sorbents has demonstrated that the most challenging aspect of developing CO{sub 2} sorbents is regeneration. The research documented in this report investigates options to improve regeneration of the CO{sub 2} capture sorbents. This research includes effort on addressing existing regeneration limitations for sorbents previously developed and new approaches that focus initially on the regeneration performance of the sorbent.

Turk, Brian; Gupta, Raghubir; Sharma, Pradeepkumar; Albritton, Johnny; Jamal, Aqil

2010-09-30T23:59:59.000Z

248

DEVELOPMENT OF DISPOSABLE SORBENTS FOR CHLORIDE REMOVAL FROM HIGH TEMPERATURE COAL-DERIVED GASES  

DOE Green Energy (OSTI)

Advanced integrated-gasification combined-cycle (IGCC) and integrated-gasification fuel cell (IGFC) systems require the development of high temperature sorbents for the removal of hydrogen chloride (HCl) vapor to less than 1 parts-per-million (ppm) levels. HCl is a highly reactive, corrosive, and toxic gas which must be removed to meet environmental regulations, to protect power generation equipment, and to minimize deterioration of hot gas desulfurization sorbents. The objective of this program was to develop disposable, alkali-based sorbents capable of reducing HCl vapor levels to less than 1 ppm in the temperature range from 400 to 750 C and pressures in the range from 1 to 20 atm. The primary areas of focus of this program were to investigate different methods of sorbent fabrication, testing their suitability for different reactor configurations, obtaining reaction kinetics data, and conducting a preliminary economic feasibility assessment. This program was a joint effort between SRI International (SRI), Research Triangle Institute (RTI), and General Electric Corporate Research and Development (GE-CRD). SRI, the prime contractor and RTI, a major subcontractor, performed most of the work in this program. Thermochemical calculations indicated that sodium-based sorbents were capable of reducing HCl vapor levels to less than 1 ppm at temperatures up to 650 C, but the regeneration of spent sorbents would require complex process steps. Nahcolite (NaHCO{sub 3}), a naturally-occurring mineral, could be used as an inexpensive sorbent to remove HCl vapor in hot coal gas streams. In the current program, nahcolite powder was used to fabricate pellets suitable for fixed-bed reactors and granules suitable for fluidized-bed reactors. Pilot-scale equipment were used to prepare sorbents in large batches: pellets by disk pelletization and extrusion techniques, and granules by granulation and spray-drying techniques. Bench-scale fixed- and fluidized-bed reactors were assembled at SRI and RTI to conduct tests at high-temperature, high-pressure conditions (HTHP). The HTHP tests confirmed the ability of nahcolite pellets and granules to reduce the HCl vapor levels to less than 1 ppm levels with a very high sorbent utilization for chloride capture. The effect of several operating variables such as temperature, pressure, presence of hydrogen sulfide, and sorbent preparation methods was studied on the efficacy of HCl removal by the sorbent. Pilot-scale tests were performed in the fluidized-bed mode at the gasifier facility at the GE-CRD. Sorbent exposure tests were also conducted using a hot coal gas stream from the DOE/FETC's fluidized-bed gasifier at Morgantown, WV. These tests confirmed the results obtained at SRI and RTI. A preliminary economic assessment showed that the cost of HCl removal in a commercial IGCC system will be about $0.001/kWh (1 mills/kWh).

Gopala Krishnan; Raghubir Gupta

1999-09-01T23:59:59.000Z

249

Synthesis of acrylates and methacrylates from coal-derived syngas. Quarterly report, October--December 1996  

SciTech Connect

Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas, under a contract from the US Department of Energy, Federal Energy Technology Center. This three-step process consists of synthesis of a propionate, its condensation with formaldehyde, and esterification of resulting methacrylic acid (MAA) with methanol to produce MMA. Eastman has focused on the propionate synthesis step. the resultant Mo catalysts work efficiently at much less severe conditions (170{degrees}C and 30 atm) than the conventional Ni catalysts (270{degrees}C and 180 atm). Bechtel has performed an extensive cost analysis which shows that Eastman`s propionate synthesis step is competitive with other technologies to produce the anhydride. In the second step, RTI and Eastman have developed active and stable V-Si-P ternary metal oxide catalysts Nb/SiO{sub 2} and Ta/SiO{sub 2} catalysts for the condensation of propionic anhydride and acid with formaldehyde. RTI has demonstrated a novel correlation among the catalyst acid-base properties, condensation reaction yield, and long-term catalyst activity. Current research focuses on enhancing the condensation reaction yields by better understanding of the acid-base property correlation, in situ condensation in a high-temperature, high- pressure (HTHP) slurry reactor, and alternate formaldehyde feedstocks. Based on Eastman and RTI laboratory data, a cost estimate is also being developed for the integrated process.

NONE

1997-05-02T23:59:59.000Z

250

COMBUSTION OF COAL IN AN OPPOSED FLOW DIFFUSION BURNER  

E-Print Network (OSTI)

P.J. and Wells, J.H. , Coal, Coke and Coal Chemicals, 108, (of coal, carbon, char. coke, and other coal derived orpulverized coal, char, coke, solvent refined coal, and coal

Chin, W.K.

2010-01-01T23:59:59.000Z

251

Hydrogen Fuel  

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

Hydrogen is a clean fuel that, when consumed, produces only water. Hydrogen can be produced from a variety of domestic sources, such as coal, natural gas, nuclear power, and renewable power. These...

252

DEVELOPMENT OF NOVEL CERAMIC NANOFILM-FIBER INTEGRATED OPTICAL SENSORS FOR RAPID DETECTION OF COAL DERIVED SYNTHESIS GAS  

DOE Green Energy (OSTI)

The overall goal of this project is to conduct fundamental studies on advanced ceramic materials and fiber optic devices for developing new types of high temperature (>500{degree}C) fiber optic chemical sensors (FOCS) for monitoring fossil (mainly coal) and biomass derived gases in power plants. The primary technical objective is to investigate and demonstrate the nanocrystalline doped-ceramic thin film enabled FOCS that possess desired stability, sensitivity and selectivity for in-situ, rapid gas detection in the syngas streams from gasification and combustion flue gases. This report summarizes research works of two integrated parts: (1) development of metal oxide solid thin films as sensing materials for detection and measurement of important gas components relevant to the coal- and biomass-derived syngas and combustion gas streams at high temperatures; and (2) development of fiber optic devices that are potentially useful for constructing FOCS in combination with the solid oxide thin films identified in this program.

Junhang Dong; Hai Xiao; Xiling Tang; Hongmin Jiang; Kurtis Remmel; Amardeep Kaur

2012-09-30T23:59:59.000Z

253

Co-firing high sulfur coal with refuse derived fuels. Technical progress report No. 6, January--March 1996  

DOE Green Energy (OSTI)

The objectives for this quarter of study on the co-firing of high sulfur coals with refuse derived fuels were two-fold. First, the effects of different experimental parameters such as temperature, flow rates and reaction times on the formation of chlorinated organic compounds were studied using the tubular furnace as a reactor followed by GC/MS analysis. Secondly, the effect of fuel/air ratio on the flue gas composition and combustion efficiency were studied with the AFBC system.

Pan, W.P.; Riley, J.T.; Lloyd, W.G.

1996-02-29T23:59:59.000Z

254

Sunlight Ancient and Modern: the Relative Energy Efficiency of Hydrogen from Coal and Current Biomass .  

E-Print Network (OSTI)

??The significance of hydrogen production is increasing as fossil fuels are being depleted and energy security is of increasing importance to the United States. Furthermore, (more)

Zhang, Ling

2004-01-01T23:59:59.000Z

255

Integrated Warm Gas Multicontaminant Cleanup Technologies for Coal-Derived Syngas  

Science Conference Proceedings (OSTI)

One of the key obstacles for the introduction of commercial gasification technology for the production of power with Integrated Gasification Combined Cycle (IGCC) plants or the production of value added chemicals, transportation fuels, and hydrogen has been the cost of these systems. This situation is particularly challenging because the United States has ample coal resources available as raw materials and effective use of these raw materials could help us meet our energy and transportation fuel needs while significantly reducing our need to import oil. One component of the cost of these systems that faces strong challenges for continuous improvement is removing the undesirable components present in the syngas. The need to limit the increase in cost of electricity to oil and natural gas. RTI, with DOE/NETL support, has been developing sorbent technologies that enable capture of trace contaminants and CO{sub 2} at temperatures above 400 °F that achieve better capture performance, lower costs and higher thermal efficiency. This report describes the specific work of sorbent development for mercury (Hg), arsenic (As), selenium (Se), cadmium (Cd), and phosphorous (P) and CO{sub 2} removal. Because the typical concentrations of Hg, As, Se, Cd, and P are less than 10 ppmv, the focus has been on single-use sorbents with sufficient capacity to ensure replacement costs are cost effective. The research in this report describes the development efforts which expand this sorbent development effort to include Se, Cd, and P as well as Hg and As. Additional research has focused on improving removal performance with the goal of achieving effluent concentrations that are suitable for chemical production applications. By contrast, sorbent development for CO{sub 2} capture has focused on regenerable sorbents that capture the CO{sub 2} byproduct at higher CO{sub 2} pressures. Previous research on CO{sub 2} sorbents has demonstrated that the most challenging aspect of developing CO{sub 2} sorbents is regeneration. The research documented in this report investigates options to improve regeneration of the CO{sub 2} capture sorbents. This research includes effort on addressing existing regeneration limitations for sorbents previously developed and new approaches that focus initially on the regeneration performance of the sorbent.

Turk, Brian; Gupta, Raghubir; Sharma, Pradeepkumar; Albritton, Johnny; Jamal, Aqil

2010-09-30T23:59:59.000Z

256

NETL: Coal & Coal Biomass to Liquids  

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

Coal Biomass to Liquids Hydrogen-from-Coal RD&D ENERGY ANALYSIS About Us Search Products Contacts SMART GRID ANALYSIS BASELINE STUDIES QUALITY GUIDELINES NETL-RUA About NETL-RUA...

257

Coal/biomass fuels and the gas turbine: Utilization of solid fuels and their derivatives  

Science Conference Proceedings (OSTI)

This paper discusses key design and development issues in utilizing coal and other solid fuels in gas turbines. These fuels may be burned in raw form or processed to produce liquids or gases in more or less refined forms. The use of such fuels in gas turbines requires resolution of technology issues which are of little or no consequence for conventional natural gas and refined oil fuels. For coal, these issues are primarily related to the solid form in which coal is naturally found and its high ash and contaminant levels. Biomass presents another set of issues similar to those of coal. Among the key areas discussed are effects of ash and contaminant level on deposition, corrosion, and erosion of turbine hot parts, with particular emphasis on deposition effects.

DeCorso, M. [Power Tech Associates, Inc., Paramus, NJ (United States); Newby, R. [Westinghouse Electric Corp., Pittsburgh, PA (United States); Anson, D. [Battelle, Columbus, OH (United States); Wenglarz, R. [Allison Engine Co., Indianapolis, IN (United States); Wright, I. [Oak Ridge National Lab., TN (United States)

1996-06-01T23:59:59.000Z

258

Refinery Integration of By-Products from Coal-Derived Jet Fuels  

Science Conference Proceedings (OSTI)

This report summarizes the accomplishments toward project goals during the first six months of the third year of the project to assess the properties and performance of coal based products. These products are in the gasoline, diesel and fuel oil range and result from coal based jet fuel production from an Air Force funded program. Specific areas of progress include generation of coal based material that has been fractionated into the desired refinery cuts, acquisition and installation of a research gasoline engine, and modification of diesel engines for use in evaluating diesel produced in the project. Characterization of the gasoline fuel indicates a dominance of single ring alkylcycloalkanes that have a low octane rating; however, blends containing these compounds do not have a negative effect upon gasoline when blended in refinery gasoline streams. Characterization of the diesel fuel indicates a dominance of 3-ring aromatics that have a low cetane value; however, these compounds do not have a negative effect upon diesel when blended in refinery diesel streams. The desulfurization of sulfur containing components of coal and petroleum is being studied so that effective conversion of blended coal and petroleum streams can be efficiently converted to useful refinery products. Equipment is now in place to begin fuel oil evaluations to assess the quality of coal based fuel oil. Combustion and characterization of fuel oil indicates that the fuel is somewhere in between a No. 4 and a No. 6 fuel oil. Emission testing indicates the fuel burns similarly to these two fuels, but trace metals for the coal-based material are different than petroleum-based fuel oils. Co-coking studies using cleaned coal are highly reproducible in the pilot-scale delayed coker. Evaluation of the coke by Alcoa, Inc. indicated that while the coke produced is of very good quality, the metals content of the carbon is still high in iron and silica. Coke is being evaluated for other possible uses. Methods to reduce metal content are being evaluated.

Caroline E. Burgess Clifford; Andre Boehman; Chunshan Song; Bruce Miller; Gareth Mitchell

2006-05-17T23:59:59.000Z

259

Development of Continuous Solvent Extraction Processes for Coal Derived Carbon Products  

SciTech Connect

This DOE NETL-sponsored effort seeks to develop continuous processes for producing carbon products from solvent-extracted coal. A key process step is removal of solids from liquefied coal. Three different processes were compared: gravity separation, centrifugation using a decanter-type Sharples Pennwalt centrifuge, and a Spinner-II centrifuge. The data suggest that extracts can be cleaned to as low as 0.5% ash level and probably lower using a combination of these techniques.

Elliot B. Kennel

2006-12-31T23:59:59.000Z

260

Development of Kilowatt-Scale Coal Fuel Cell Technology - DOE Hydrogen and Fuel Cells Program FY 2012 Annual Progress Report  

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

5 5 FY 2012 Annual Progress Report DOE Hydrogen and Fuel Cells Program Steven S.C. Chuang (Primary Contact), Tritti Siengchum, Jelvehnaz Mirzababaei, Azadeh Rismanchian, and Seyed Ali Modjtahedi The University of Akron 302 Buchtel Common Akron, OH 44310-3906 Phone: (330) 972-6993 Email: schuang@uakron.edu DOE Managers HQ: Dimitrios Papageorgopoulos Phone: (202) 586-5463 Email: Dimitrios.Papageorgopoulos@ee.doe.gov GO: Reg Tyler Phone: (720) 356-1805 Email: Reginald.Tyler@go.doe.gov Contract Number: DE-FC36-08GO0881114 Project Start Date: June 1, 2008 Project End Date: May 31, 2012 *Congressionally directed project Fiscal Year (FY) 2012 Objectives To develop a kilowatt-scale coal-based solid oxide fuel cell (SOFC) technology. The outcome of this research effort

Note: This page contains sample records for the topic "hydrogen coal derived" from the National Library of EnergyBeta (NLEBeta).
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they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
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261

Production of High Purity Hydrogen from Domestic Coal: Assessing the Techno-Economic Impact of Emerging Technologies  

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

Production of High Purity Production of High Purity Hydrogen from Domestic Coal: Assessing the Techno-Economic Impact of Emerging Technologies August 30, 2010 DOE/NETL-2010/1432 Disclaimer This report was prepared as an account of work sponsored by an agency of the United States (U.S.) government. Neither the U.S., nor any agency thereof, nor any of their employees, nor any of their contractors, subcontractors, or their employees makes any warranty, expressed or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily

262

Hydrogen Fuel Basics | Department of Energy  

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

Hydrogen Fuel Basics Hydrogen Fuel Basics Hydrogen Fuel Basics August 14, 2013 - 2:06pm Addthis Hydrogen is a clean fuel that, when consumed, produces only water. Hydrogen can be produced from a variety of domestic sources, such as coal, natural gas, nuclear power, and renewable power. These qualities make it an attractive fuel option for transportation and electricity generation applications. Hydrogen is an energy carrier that can be used to store, move, and deliver energy produced from other sources. The energy in hydrogen fuel is derived from the fuels and processes used to produce the hydrogen. Today, hydrogen fuel can be produced through several methods. The most common methods are thermal, electrolytic, and photolytic processes. Thermal Processes Thermal processes for hydrogen production typically involve steam

263

Hydrogen Fuel Basics | Department of Energy  

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

Hydrogen Fuel Basics Hydrogen Fuel Basics Hydrogen Fuel Basics August 14, 2013 - 2:06pm Addthis Hydrogen is a clean fuel that, when consumed, produces only water. Hydrogen can be produced from a variety of domestic sources, such as coal, natural gas, nuclear power, and renewable power. These qualities make it an attractive fuel option for transportation and electricity generation applications. Hydrogen is an energy carrier that can be used to store, move, and deliver energy produced from other sources. The energy in hydrogen fuel is derived from the fuels and processes used to produce the hydrogen. Today, hydrogen fuel can be produced through several methods. The most common methods are thermal, electrolytic, and photolytic processes. Thermal Processes Thermal processes for hydrogen production typically involve steam

264

A GIS-based Assessment of Coal-based Hydrogen Infrastructure Deployment in the State of Ohio  

E-Print Network (OSTI)

electricity and CO 2 from coal with commercially readyHong B, Slatick E. Carbon dioxide emission factors for coal.EIA Quarterly Coal Report JanuaryApril 1994:18. 1994. DOE/

Johnson, Nils; Yang, Christopher; Ogden, J

2009-01-01T23:59:59.000Z

265

Predicting extents of mercury oxidation in coal-derived flue gases  

SciTech Connect

The extent of Hg oxidation determines the portion of Hg in the flue gas from a coal-fired power station that can be removed in SO{sub 2} scrubbers. This article evaluates predicted extents of Hg oxidation from a detailed chemical reaction mechanism, emphasizing the data from 1 and 29 MW pilotscale furnaces for diverse coal types. The proposed mercury (Hg) oxidation mechanism consists of a 168-step gas phase mechanism that accounts for interaction among all important flue gas species and a heterogeneous oxidation mechanism on unburned carbon (UBC) particles, similar to established chemistry for dioxin production under comparable conditions. The mechanism was incorporated into a gas cleaning system simulator to predict the proportions of elemental and oxidized Hg species in the flue gases, given relevant coal properties (C/H/O/N/S/Cl/Hg), flue gas composition (O{sub 2}, H{sub 2}O, HCl), emissions (NOx, SOx, CO), the recovery of fly ash, fly ash loss-on-ignition (LOI), and a thermal history. Predictions are validated without parameter adjustments against datasets from lab-scale and from pilot-scale coal furnaces at 1 and 29 MWt. Collectively, the evaluations cover 16 coals representing ranks from sub-bituminous through high-volatile bituminous, including cases with Cl{sub 2} and CaCl{sub 2} injection. The predictions are, therefore, validated over virtually the entire domain of Cl-species concentrations and UBC levels of commercial interest. Additional predictions identify the most important operating conditions in the furnace and gas cleaning system, including stoichiometric ratio, NOX, LOI, and residence time, as well as the most important coal properties, including coal-Cl. 33 refs., 4 figs., 3 tabs.

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

2005-07-01T23:59:59.000Z

266

Zero emission coal: a future source of clean electric power and hydrogen  

DOE Green Energy (OSTI)

The pairing of two novel technologies may permit coal energy to satisfy a dramatically increasing world energy demand for the next few hundred years. This can be done while virtually eliminating not only airborne SO{sub x}, NO{sub x}, mercury and particulate emissions, but also the main greenhouse gas, carbon dioxide (CO{sub 2}). The Zero Emission Coal Alliance, a collaboration of approximately 20 international industrial and government entities is investigating these concepts with the objective of completing the first pilot plant within 5 years. Paradoxically, climate change was not the overriding consideration that drove the development of these inventions. The more important consideration was that, if world carbon use continues to accelerate at rates even close to those in the last century, carbon from fossil fuels will overwhelm the natural CO{sub 2} sinks. In this view, the 'Kyoto' objectives are almost meaningless and misdirect enormous resources - both human and financial. If a world population of 10 billion reaches a standard of living comaprable, on the average, to that of the US in 2000 (with similar carbon use), then world yearly CO{sub 2} emissions will be ten times their current level. Carbon (in the form of coal) is our most important energy resource. The Challenge is to find sustainable ways of using it.

Ziock, H. J. (Hans-Joachim)

2001-01-01T23:59:59.000Z

267

Hydrogen  

U.S. Energy Information Administration (EIA)

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

268

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

269

Center for Coal-Derived Low Energy Materials for Sustainable Construction  

SciTech Connect

The overarching goal of this project was to create a sustained center to support the continued development of new products and industries that manufacture construction materials from coal combustion by-products or CCBs (e.g., cements, grouts, wallboard, masonry block, fillers, roofing materials, etc). Specific objectives includes the development of a research kiln and associated system and the formulation and production of high performance low-energy, low-CO2 emitting calcium sulfoaluminate (CAS) cement that utilize coal combustion byproducts as raw materials.

Jewell, Robert; Robl, Tom; Rathbone, Robert

2012-06-30T23:59:59.000Z

270

Coal liquefaction process  

DOE Patents (OSTI)

An improved coal liquefaction process is provided which enables conversion of a coal-oil slurry to a synthetic crude refinable to produce larger yields of gasoline and diesel oil. The process is characterized by a two-step operation applied to the slurry prior to catalytic desulfurization and hydrogenation in which the slurry undergoes partial hydrogenation to crack and hydrogenate asphaltenes and the partially hydrogenated slurry is filtered to remove minerals prior to subsequent catalytic hydrogenation.

Karr, Jr., Clarence (Morgantown, WV)

1977-04-19T23:59:59.000Z

271

Liquefaction of sub-bituminous coal  

SciTech Connect

Sub-bituminous coal is directly liquefied in two stages by use of a liquefaction solvent containing insoluble material as well as 850.degree. F.+ material and 850.degree. F.- material derived from the second stage, and controlled temperature and conversion in the second stage. The process is in hydrogen balance.

Schindler, Harvey D. (Fair Lawn, NJ); Chen, James M. (Edison, NJ)

1986-01-01T23:59:59.000Z

272

A GIS-based Assessment of Coal-based Hydrogen Infrastructure Deployment in the State of Ohio  

E-Print Network (OSTI)

6 Coal price (2005$) $1.29/MMBTU 93.8 kg CO 2 /MMBTU coal COsales $0.05/kWh price (2005$) Coal type Illinois no.coal-to- electricity ef?ciency is 37%, carbon capture is 91%, and the electricity price

Johnson, Nils; Yang, Christopher; Ogden, J

2009-01-01T23:59:59.000Z

273

Toxicity of shale oil to freshwater algae: comparisons with petroleum and coal-derived oils  

DOE Green Energy (OSTI)

The toxicities of various water-soluble fractions of Paraho/SOHIO shale oils and coal liquefaction products to the algae Selenastrum capricornutum and Microcystis aeruginosa are investigated. Photosynthetic inhibition is the criterion of toxicity. A secondary objective of the algal bioassay is determination of the range of toxic concentrations. (ACR)

Giddings, J.M.

1980-01-01T23:59:59.000Z

274

Hydrogen Production and Purification from Coal and Other Heavy Feedstocks Year 6 - Activity 1.4 - Development of a National Center for Hydrogen Technology  

SciTech Connect

Air Products and Chemicals, Inc., is developing the sour pressure swing adsorption (PSA) technology which can be used to reject acid gas components (hydrogen sulfide [H{sub 2}S] and carbon dioxide [CO{sub 2}]) from sour syngas streams such as coal gasification syngas. In the current work, tests were conducted to investigate the impact of continuous exposure of real sour syngas and dilute levels of hydrochloric acid (HCl) and ammonia (NH{sub 3}) on the preferred adsorbent of that process. The results show a modest (~10%15%) decrease in CO{sub 2} adsorption capacity after sour syngas exposure, as well as deposition of metals from carbonyl decomposition. Continuous exposure to HCl and NH{sub 3} yield a higher degree of CO{sub 2} capacity degradation (up to 25%). These tests represent worst-case approaches since the exposure is continuous and the HCl and NH{sub 3} levels are relatively high compare to an industrial sour syngas stream. Long-term PSA tests are needed to unequivocally evaluate the impact of cyclic exposure to these types of streams.

Dunham, Grant

2012-03-15T23:59:59.000Z

275

Chemicals from coal  

Science Conference Proceedings (OSTI)

This chapter contains sections titled: Chemicals from Coke Oven Distillate; The Fischer-Tropsch Reaction; Coal Hydrogenation; Substitute Natural Gas (SNG); Synthesis Gas Technology; Calcium Carbide; Coal and the Environment; and Notes and References

Harold A. Wittcoff; Bryan G. Reuben; Jeffrey S. Plotkin

2004-12-01T23:59:59.000Z

276

Development of Mercury and Hydrogen Chloride Emission Monitors for Coal Gasifiers  

SciTech Connect

The gas conditioning issues involved with coal gasification streams are very complex and do not have simple solutions. This is particularly true in view of the fact that the gas conditioning system must deal with tars, high moisture contents, and problems with NH{sub 3} without affecting low ppb levels of Hg, low levels (low ppm or less) of HCl, or the successful operation of conditioner components and analytical systems. Those issues are far from trivial. Trying to develop a non-chemical system for gas conditioning was very ambitious in view of the difficult sampling environment and unique problems associated with coal gasification streams. Although a great deal was learned regarding calibration, sample transport, instrumentation options, gas stream conditioning, and CEM design options, some challenging issues still remain. Sample transport is one area that is often not adequately considered. Because of the gas stream composition and elevated temperatures involved, special attention will need to be given to the choice of materials for the sample line and other plumbing components. When using gas stream oxidation, there will be sample transport regions under oxidizing as well as reducing conditions, and each of those regions will require different materials of construction for sample transport. The catalytic oxidation approach worked well for removal of tars and NH{sub 3} on a short term basis, but durability issues related to using the catalyst tube during extended testing periods still require study.

G. Norton; D. Eckels; C. Chriswell

2001-02-26T23:59:59.000Z

277

Catalysts for upgrading coal-derived liquids. Quarterly report, October 1-December 31, 1980  

DOE Green Energy (OSTI)

A linear relationship represents the hydrogenation activity decay of catalysts used in four experimental runs reported previously. The weight percent hydrogen in the reactor product oils plotted against oil-catalyst contact time for experimental runs ZBB, ZBC, ZBD, and ZBE reveals a linear decay rate of 0.0083 wt% hydrogen per hour. This is one quantitative measure of catalyst activity decay. The data for the plot incorporate three different catalysts or combinations used to process a PAMCO liquid at 1500 psig, 435C and LVHST of 2 hours. The data set covers run duration of up to 120 hours of oil-catalyst contact. An air driven hydrogen compressor was installed in the Catalyst Life Test Unit to reduce the costs associated with bottle hydrogen. Minor repairs were made on the oil feed pump. Five experimental runs were made with Shell 324 NiMo/Al catalyst using two feedstocks: (1) 40 wt% EDS/EDS raw solvent and (2) 30 wt% SRC-I creosote oil. The EDS feed oil proved to be rather easily hydrotreated as evidenced by 82 to 100% nitrogen removal, essentially complete desulfurization and no catalyst activity decay during 260 hours of continuous operation. Rapid coking resulted from the highly hydrogen deficient SRC/creosote mixture. The Shell 324 catalyst gave excellent hydrogenation of both liquids by increasing the hydrogen content of the product oils by about 3.8 wt%. This catalyst will be used in future studies; however, a new feedstock consisting of 30 wt% SRC-I/PAMCO process solvent will be assessed for use in catalyst decay mechanism studies.

Crynes, B.L.

1981-01-14T23:59:59.000Z

278

Refinery Integration of By-Products from Coal-Derived Jet Fuels  

SciTech Connect

This report summarizes the accomplishments toward project goals during the second six months of the third year of the project to assess the properties and performance of coal based products. These products are in the gasoline, diesel and fuel oil range and result from coal based jet fuel production from an Air Force funded program. Specific areas of progress include generation of coal based material that has been fractionated into the desired refinery cuts and examination of carbon material, the use of a research gasoline engine to test coal-based gasoline, and modification of diesel engines for use in evaluating diesel produced in the project. At the pilot scale, the hydrotreating process was modified to separate the heavy components from the LCO and RCO fractions before hydrotreating in order to improve the performance of the catalysts in further processing. Characterization of the gasoline fuel indicates a dominance of single ring alkylcycloalkanes that have a low octane rating; however, blends containing these compounds do not have a negative effect upon gasoline when blended in refinery gasoline streams. Characterization of the diesel fuel indicates a dominance of 3-ring aromatics that have a low cetane value; however, these compounds do not have a negative effect upon diesel when blended in refinery diesel streams. Both gasoline and diesel continue to be tested for combustion performance. The desulfurization of sulfur containing components of coal and petroleum is being studied so that effective conversion of blended coal and petroleum streams can be efficiently converted to useful refinery products. Activated carbons have proven useful to remove the heavy sulfur components, and unsupported Ni/Mo and Ni/Co catalysts have been very effective for hydrodesulfurization. Equipment is now in place to begin fuel oil evaluations to assess the quality of coal based fuel oil. Combustion and characterization of the latest fuel oil (the high temperature fraction of RCO from the latest modification) indicates that the fraction is heavier than a No. 6 fuel oil. Combustion efficiency on our research boiler is {approx}63% for the heavy RCO fraction, lower than the combustion performance for previous co-coking fuel oils and No. 6 fuel oil. An additional coal has been procured and is being processed for the next series of delayed co-coking runs. Work continues on characterization of liquids and solids from co-coking of hydrotreated decant oils; liquid yields include more saturated and hydro- aromatics, while the coke quality varies depending on the conditions used. Pitch material is being generated from the heavy fraction of co-coking. Investigation of coal extraction as a method to produce RCO continues; the reactor modifications to filter the products hot and to do multi-stage extraction improve extraction yields from {approx}50 % to {approx}70%. Carbon characterization of co-cokes for use as various carbon artifacts continues.

Caroline E. Burgess Clifford; Andre' Boehman; Chunshan Song; Bruce Miller; Gareth Mitchell

2006-09-17T23:59:59.000Z

279

Bimetallic promotion of cooperative hydrogen transfer and heteroatom removal in coal liquefaction. Final technical report, September 1, 1988--December 31, 1991  

DOE Green Energy (OSTI)

The ultimate objective of this research has been to uncover novel reagents and experimental conditions for heteroatom removal and hydrogen transfer processes, which would be applicable to the liquefaction of coal under low-severity conditions. To this end, one phase of this research has investigated the cleavage of carbon-heteroatom bonds involving sulfur, oxygen, nitrogen and halogen by subvalent transition-metal complexes. A second phase of the study has assessed the capability of the same transition-metal complexes or of organoaluminum Lewis acids to catalyze the cleavage of carbon-hydrogen bonds in aromatics and hence to promote hydrogen shuttling. Finally, a third phase of our work has uncovered a remarkable synergistic effect of combinations of transition metals with organoaluminum Lewis acids on hydrogen shuttling between aromatics and hydroaromatics. (VC)

Eisch, J.J.

1992-04-07T23:59:59.000Z

280

Assessing Strategies for Fuel and Electricity Production in a California Hydrogen Economy  

E-Print Network (OSTI)

production of hydrogen, electricity and CO 2 from coal withproduction of hydrogen, electricity, and CO 2 from coal withDecarbonized hydrogen and electricity from natural gas.

McCarthy, Ryan; Yang, Christopher; Ogden, Joan M.

2008-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

Hydrogen Generation from Biomass-Derived Surgar Alcohols via the Aqueous-Phase Carbohydrate Reforming (ACR) Process  

DOE Green Energy (OSTI)

This project involved the investigation and development of catalysts and reactor systems that will be cost-effective to generate hydrogen from potential sorbitol streams. The intention was to identify the required catalysts and reactors systems as well as the design, construction, and operation of a 300 grams per hour hydrogen system. Virent was able to accomplish this objective with a system that generates 2.2 kgs an hour of gas containing both hydrogen and alkanes that relied directly on the work performed under this grant. This system, funded in part by the local Madison utility, Madison, Gas & Electric (MGE), is described further in the report. The design and development of this system should provide the necessary scale-up information for the generation of hydrogen from corn-derived sorbitol.

Randy Cortright

2006-06-30T23:59:59.000Z

282

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. Table 1 provides an overview of the major markets for carbon products. Current sources of materials for these processes generally rely on petroleum distillation products or coal tar distillates obtained as a byproduct of metcoke production facilities. In the former case, the American materials industry, just as the energy industry, is dependent upon foreign sources of petroleum. In the latter case, metcoke production is decreasing every year due to the combined difficulties associated with poor economics and a significant environmental burden. Thus, a significant need exists for an environmentally clean process which can used domestically obtained raw materials and which can still be very competitive economically.

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

2005-04-13T23:59:59.000Z

283

Co-firing high sulfur coal with refuse derived fuels. Final report  

DOE Green Energy (OSTI)

This project was designed to evaluate the combustion performance of and emissions from a fluidized bed combustor during the combustion of mixtures of high sulfur and/or high chlorine coals and municipal solid waste (MSW). The project included four major tasks, which were as follows: (1) Selection, acquisition, and characterization of raw materials for fuels and the determination of combustion profiles of combination fuels using thermal analytical techniques; (2) Studies of the mechanisms for the formation of chlorinated organics during the combustion of MSW using a tube furnace; (3) Investigation of the effect of sulfur species on the formation of chlorinated organics; and (4) Examination of the combustion performance of combination fuels in a laboratory scale fluidized bed combustor. Several kinds of coals and the major combustible components of the MSW, including PVC, newspaper, and cellulose were tested in this project. Coals with a wide range of sulfur and chlorine contents were used. TGA/MS/FTIR analyses were performed on the raw materials and their blends. The possible mechanism for the formation of chlorinated organics during combustion was investigated by conducting a series of experiments in a tube furnace. The effect of sulfur dioxide on the formation of molecular chlorine during combustion processes was examined in this study.

Pan, W.P.; Riley, J.T.; Lloyd, W.G.

1997-11-30T23:59:59.000Z

284

Energy Basics: Hydrogen Fuel  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

EERE: Energy Basics Hydrogen Fuel Hydrogen is a clean fuel that, when consumed, produces only water. Hydrogen can be produced from a variety of domestic sources, such as coal,...

285

Optical Fiber Chemical Sensor with Sol-Gel Derived Refractive Material as Transducer for High Temperature Gas Sensing in Clean Coal Technology  

SciTech Connect

The chemistry of sol-gel derived silica and refractive metal oxide has been systematically studied. Sol-gel processes have been developed for preparing porous silica and semiconductor metal oxide materials. Micelle/reversed micelle techniques have been developed for preparing nanometer sized semiconductor metal oxides and noble metal particles. Techniques for doping metal ions, metal oxides and nanosized metal particles into porous sol-gel material have also been developed. Optical properties of sol-gel derived materials in ambient and high temperature gases have been studied by using fiber optic spectroscopic techniques, such as fiber optic ultraviolet/visible absorption spectrometry, fiber optic near infrared absorption spectrometry and fiber optic fluorescence spectrometry. Fiber optic spectrometric techniques have been developed for investigating the optical properties of these sol-gel derived materials prepared as porous optical fibers or as coatings on the surface of silica optical fibers. Optical and electron microscopic techniques have been used to observe the microstructure, such as pore size, pore shape, sensing agent distribution, of sol-gel derived material, as well as the size and morphology of nanometer metal particle doped in sol-gel derived porous silica, the nature of coating of sol-gel derived materials on silica optical fiber surface. In addition, the chemical reactions of metal ion, nanostructured semiconductor metal oxides and nanometer sized metal particles with gas components at room temperature and high temperatures have also been investigated with fiber optic spectrometric methods. Three classes of fiber optic sensors have been developed based on the thorough investigation of sol-gel chemistry and sol-gel derived materials. The first group of fiber optic sensors uses porous silica optical fibers doped with metal ions or metal oxide as transducers for sensing trace NH{sub 3} and H{sub 2}S in high temperature gas samples. The second group of fiber optic sensors uses sol-gel derived porous silica materials doped with nanometer particles of noble metals in the form of fiber or coating for sensing trace H{sub 2}, NH{sub 3} and HCl in gas samples at for applications ambient temperature. The third classes of fiber optic sensors use sol-gel derived semiconductor metal oxide coating on the surface of silica optical fiber as transducers for selectively sensing H{sub 2}, CH{sub 4} and CO at high temperature. In addition, optical fiber temperature sensors use the fluorescence signal of rare-earth metal ions doped porous silica optical fiber or the optical absorption signal of thermochromic metal oxide materials coated on the surface of silica optical fibers have also been developed for monitoring gas temperature of corrosive gas. Based on the results obtained from this project, the principle of fiber optic sensor techniques for monitoring matrix gas components as well as trace components of coal gasification derived syngas has been established. Prototype sensors for sensing trace ammonia and hydrogen sulfide in gasification derived syngas have been built up in our laboratory and have been tested using gas samples with matrix gas composition similar to that of gasification derived fuel gas. Test results illustrated the feasibility of these sensors for applications in IGCC processes.

Shiquan Tao

2006-12-31T23:59:59.000Z

286

The economical production of alcohol fuels from coal-derived synthesis gas. Sixth quarterly technical progress report, January 1, 1993--March 31, 1993  

Science Conference Proceedings (OSTI)

Preliminary economic investigations have focused on cost reduction measures in the production of syngas from coal. A spread sheet model has been developed which can determine the cost of syngas production based upon the cost of equipment and raw materials and the market value of energy and by-products. In comparison to natural gas derived syngas, coal derived syngas is much more expensive, suggesting a questionable economic status of coal derived alcohol fuels. While it is possible that use of less expensive coal or significant integration of alcohol production and electricity production may reduce the cost of coal derived syngas, it is unlikely to be less costly to produce than syngas from natural gas. Fuels evaluation is being conducted in three parts. First, standard ASTM tests are being used to analyze the blend characteristics of higher alcohols. Second, the performance characteristics of higher alcohols are being evaluated in a single-cylinder research engine. Third, the emissions characteristics of higher alcohols are being investigated. The equipment is still under construction and the measurement techniques are still being developed. Of particular interest is n-butanol, since the MoS{sub 2} catalyst produces only linear higher alcohols. There is almost no information on the combustion and emission characteristics of n-butanol, hence the importance of gathering this information in this research.

Not Available

1993-04-01T23:59:59.000Z

287

Co-firing high sulfur coal with refuse derived fuels. Technical report {number_sign}4  

DOE Green Energy (OSTI)

In order to study combustion performance under conditions similar to that in the AFBC system, the authors conducted a series of experiments at a heating rate of 100 C/min using the TGA/FTIR/MS system. Results indicate that more hydrocarbons are evolved at the faster heating rate, owing to incomplete combustion of the fuel. Chlorinated organic compounds can be formed at high heating rates. Certain oxidation products such as organic acids and alcohols are obtained at the slow heating rate. To simulate the conditions used in the atmospheric fluidized bed combustor (AFBC) at Western Kentucky University, studies were also conducted using a quartz tube in a tube furnace. The temperature conditions were kept identical to those of the combustor. The products evolved from the combustion of coal, PVC, and mixtures of the two were trapped in suitable solvents at different temperatures, and analyzed using the Shimadzu GC/MS system. The detection limits and the GC/MS analytical parameters were also established. The experiments were conducted keeping in mind the broader perspective; that of studying conditions conducive to the formation of chlorinated organic compounds from the combustion of coal/MSW blends. 32 figs., 16 tabs.

Pan, W.P.; Riley, J.T.; Lloyd, W.G.

1995-08-03T23:59:59.000Z

288

Development of alternative fuels from coal-derived syngas. Quarterly status report No. 6, January 1--March 31, 1992  

SciTech Connect

The overall objectives of this program are to investigate potential technologies for the conversion of coal-derived synthesis gas to oxygenated fuels, hydrocarbon fuels, fuel intermediates, and octane enhancers; and to demonstrate the most promising technologies at DOE`s LaPorte, Texas, Slurry Phase Alternative Fuels Development Unit (AFDU). BASF continues to have difficulties in scaling-up the new isobutanol synthesis catalyst developed in Air Products` laboratories. Investigations are proceeding, but the proposed operation at LaPorte in April is now postponed. DOE has accepted a proposal to demonstrate Liquid Phase Shift (LPS) chemistry at LaPorte as an alternative to isobutanol. There are two principal reasons for carrying out this run. First, following the extensive modifications at the site, operation on a relatively ``benign`` system is needed before we start on Fischer-Tropsch technology in July. Second, use of shift catalyst in a slurry reactor will enable DOE`s program on coal-based Fischer-Tropsch to encompass commercially available cobalt catalysts-up to now they have been limited to iron-based catalysts which have varying degrees of shift activity. In addition, DOE is supportive of continued fuel testing of LaPorte methanol-tests of MIOO at Detroit Diesel have been going particularly well. LPS offers the opportunity to produce methanol as the catalyst, in the absence of steam, is active for methanol synthesis.

Brown, D.M.

1992-05-19T23:59:59.000Z

289

Prediction of thermodynamic properties of coal derivatives. Annual technical report, March 1, 1991--February 28, 1992  

Science Conference Proceedings (OSTI)

The purpose of this research program is to understand and model the effect of the different intermolecular forces on the thermodynamic properties of systems containing pure compounds and mixtures. The compounds under consideration vary considerably in size, shape and energy. Therefore in order to develop a theory capable of describing accurately the thermodynamic properties and phase behavior of such systems over a wide range of temperature and pressure, one has to take into account explicitly the differences in shape and size among the various compounds as well as the different type of intermolecular interactions. In order to get a better understanding of the intermolecular forces and to test some of our recent models, we have performed considerable experimental work. We used FTIR to examine hydrogen bonding interactions between small molecules and between small molecules and polymers. In addition, we investigated experimentally the high pressure phase behavior of ternary and quaternary systems exhibiting polar and hydrogen bonding interactions.

Donohue, M.D.

1991-10-01T23:59:59.000Z

290

Advanced liquefaction using coal swelling and catalyst dispersion techniques. Volume 2, appendices. Final technical report, October 1, 1991--September 30, 1994  

Science Conference Proceedings (OSTI)

Liquefaction experiments were undertaken using subbituminous Black Thunder mine coal to observe the effects of aqueous SO{sub 2} coal beneficiation and the introduction of various coal swelling solvents and catalyst precursors. Aqueous SO{sub 2} beneficiation of Black Thunder coal removed alkali metals and alkaline earth metals, increased the sulfur content and increased the catalytic liquefaction conversion to THF solubles compared to untreated Black Thunder coal. The liquefaction solvent had varying effects on coal conversion, depending upon the type of solvent added. The hydrogen donor solvent, dihydroanthracene, was most effective, while a coal-derived Wilsonville solvent promoted more coal conversion than did relatively inert 1-methylnaphthalene. Swelling of coal with hydrogen bonding solvents tetrahydrofuran (THF), isopropanol, and methanol, prior to reaction resulted in increased noncatalytic conversion of both untreated and SO{sub 2} treated Black Thunder coals, while dimethylsulfoxide (DMSO), which was absorbed more into the coal than any other swelling solvent, was detrimental to coal conversion. Swelling of SO{sub 2} treated coal before liquefaction resulted in the highest coal conversions; however, the untreated coal showed the most improvements in catalytic reactions when swelled in either THF, isopropanol, or methanol prior to liquefaction. The aprotic solvent DMSO was detrimental to coal conversion.

Curtis, C.W. [Auburn Univ., AL (United States); Chander, S. [Pennsylvania State Univ., College Park, PA (United States); Gutterman, C.

1995-04-01T23:59:59.000Z

291

Co-firing high sulfur coal with refuse derived fuels. Technical progress report No. 8, July 1996--August 1996  

DOE Green Energy (OSTI)

The objective of this study was to examine the possible formation of chlorinated organic compounds during the combustion of blends of refuse derived fuels (RDF) and coal under conditions similar to those of an atmospheric fluidized bed combustion (AFBC) system. A series of experiments were conducted using a TGA interfaced to FTIR. Additional experiments using a tube furnace preheated to AFBC operating temperatures were also conducted. The combustion products were cryogenically trapped and analyzed with a GC/MS system. The chlorination of phenols and the condensation reactions of chlorophenols were investigated in this study. A possible mechanism for the formation of chlorinated organic compounds such as dibenzodioxins and dibenzofurans, by chlorination and condensation reactions involving phenols, was proposed.

Pan, Wei-Ping; Riley, J.T.; Lloyd, W.G.

1996-08-31T23:59:59.000Z

292

BSA 12-45: Biomass-derived Hydrogen-evolution catalyst and ...  

A simply made, inexpensive combination of biomass and earth-abundant metals has resulted in a durable catalyst for splitting water into oxygen and hydrogen, which can ...

293

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, efforts have focused on the development of carbon electrodes for Direct Carbon Fuel Cells (DCFC), and on carbon foam composites used in ballistic armor, as well as the hydrotreatment of solvents used in the basic solvent extraction process. A major goal is the production of 1500 pounds of binder pitch, corresponding to about 3000 pounds of hydrotreated solvent.

Elliot B. Kennel; Quentin C. Berg; Stephen P. Carpenter; Dady Dadyburjor; Jason C. Hissam; Manoj Katakdaunde; Liviu Magean; Abha Saddawi; Alfred H. Stiller; John W. Zondlo

2006-03-07T23:59:59.000Z

294

Effects of coal-derived trace species on the performance of molten carbonate fuel cells  

DOE Green Energy (OSTI)

The overall objective of the present study was to determine in detail the interaction effects of 10 simultaneously present, coal-gas contaminants, both on each other and on components of the Carbonate Fuel Cell. The primary goal was to assess underlying chemistries and reaction mechanisms which may cause decay in fuel cell performance or endurance as a result of both physics-chemical and/or mechanical interactions with the cell components and internal fuel cell parts. It was found, both from theory and cell test evidence, that trace contaminant interactions may occur with: Fuel-cell Electrodes (e.g., in this study with the Ni-anode), Lithium/Potassium Carbonate Electrolyte, Nickel and SS-Hardware, and by Mechanical Obstruction of Gas Flow in the Anode Plenum.

Pigeaud, A.

1991-10-01T23:59:59.000Z

295

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

296

Effects of low-temperature catalytic pretreatments on coal structure and reactivity in liquefaction. Final technical report, Volume 2 - hydrogenative and hydrothermal pretreatments and spectroscopic characterization using pyrolysis-GC-MS, CPMAS {sup 13}C NMR and FT-IR  

Science Conference Proceedings (OSTI)

It has been indicated by DOE COLIRN panel that low-temperature catalytic pretreatment is a promising approach to the development of an improved liquefaction process. This work is a fundamental study on effects of pretreatments on coal structure and reactivity in liquefaction. The main objectives of this project are to study the coal structural changes induced by low-temperature catalytic and thermal pretreatments by using spectroscopic techniques; and to clarify the pretreatment-induced changes in reactivity or convertibility of coals. As the second volume of the final report, here we summarize our work on spectroscopic characterization of four raw coals including two subbituminous coals and two bituminous coals, tetrahydrofuran (THF)-extracted but unreacted coals, the coals (THF-insoluble parts) that have been thermally pretreated. in the absence of any solvents and in the presence of either a hydrogen-donor solvent or a non-donor solvent, and the coals (THF-insoluble parts) that have been catalytically pretreated in the presence of a dispersed Mo sulfide catalyst in the absence of any solvents and in the presence of either a hydrogen-donor solvent or a non-donor solvent.

Chunshan Song; Hatcher, P.G.; Saini, A.K.; Wenzel, K.A.

1998-01-01T23:59:59.000Z

297

REFORMULATION OF COAL-DERIVED TRANSPORTATION FUELS: SELECTIVE OXIDATION OF CARBON MONOXIDE ON METAL FOAM CATALYSTS  

DOE Green Energy (OSTI)

Hydrocarbon fuels must be reformed in a series of steps to provide hydrogen for use in proton exchange membrane fuel cells (PEMFCs). Preferential oxidation (PROX) is one method to reduce the CO concentration to less than 10 ppm in the presence of {approx}40% H{sub 2}, CO{sub 2}, and steam. This will prevent CO poisoning of the PEMFC anode. Structured supports, such as ceramic monoliths, can be used for the PROX reaction. Alternatively, metal foams offer a number of advantages over the traditional ceramic monolith.

Paul Chin; Xiaolei Sun; George W. Roberts; Amornmart Sirijarhuphan; Sourabh Pansare; James G. Goodwin Jr; Richard W. Rice; James J. Spivey

2005-06-01T23:59:59.000Z

298

Method for coal liquefaction  

SciTech Connect

A process is disclosed for coal liquefaction in which minute particles of coal in intimate contact with a hydrogenation catalyst and hydrogen arc reacted for a very short time at a temperature in excess of 400.degree. C. at a pressure of at least 1500 psi to yield over 50% liquids with a liquid to gaseous hydrocarbon ratio in excess of 8:1.

Wiser, Wendell H. (Kaysville, UT); Oblad, Alex G. (Salt Lake City, UT); Shabtai, Joseph S. (Salt Lake City, UT)

1994-01-01T23:59:59.000Z

299

The economical production of alcohol fuels from coal-derived synthesis gas. Quarterly technical progress report Number 8, 1 July, 1993--30 September, 1993  

DOE Green Energy (OSTI)

Task 1, the preparation of catalyst materials, is proceeding actively. At WVU, catalysts based on Mo are being prepared using a variety of approaches to alter the oxidation state and environment of the Mo. At UCC and P, copper-based zinc chromite spinel catalysts will be prepared and tested. The modeling of the alcohol-synthesis reaction in a membrane reactor is proceeding actively. Under standard conditions, pressure drop in the membrane reactor has been shown to be negligible. In Task 2, base case designs had previously been completed with a Texaco gasifier. Now, similar designs have been completed using the Shell gasifier. A comparison of the payback periods or production cost of these plants shows significant differences among the base cases. However, a natural gas only design, prepared for comparison purposes, gives a lower payback period or production cost. Since the alcohol synthesis portion of the above processes is the same, the best way to make coal-derived higher alcohols more attractive economically than natural gas-derived higher alcohols is by making coal-derived syngas less expensive than natural gas-derived syngas. The maximum economically feasible capacity for a higher alcohol plant from coal-derived syngas appears to be 32 MM bbl/yr. This is based on consideration of regional coal supply in the eastern US, coal transportation, and regional product demand. The benefits of economics of scale are illustrated for the base case designs. A value for higher alcohol blends has been determined by appropriate combination of RVP, octane number, and oxygen content, using MTBE as a reference. This analysis suggests that the high RVP of methanol in combination with its higher water solubility make higher alcohols more valuable than methanol.

Not Available

1993-10-01T23:59:59.000Z

300

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

Note: This page contains sample records for the topic "hydrogen coal derived" from the National Library of EnergyBeta (NLEBeta).
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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

PRODUCTION OF FOAMS, FIBERS AND PITCHES USING A COAL EXTRACTION PROCESS  

DOE Green Energy (OSTI)

This Department of Energy National Energy Technology Laboratory sponsored project developed processes for converting coal feedstocks to carbon products, including coal-derived pitch, coke foams and fibers based on solvent extraction processes. A key technology is the use of hydrogenation accomplished at elevated temperatures and pressures to obtain a synthetic coal pitch. Hydrogenation, or partial direct liquefaction of coal, is used to modify the properties of raw coal such that a molten synthetic pitch can be obtained. The amount of hydrogen required to produce a synthetic pitch is about an order of magnitude less than the amount required to produce synthetic crude oil. Hence the conditions for synthetic pitch production consume very little hydrogen and can be accomplished at substantially lower pressure. In the molten state, hot filtration or centrifugation can be used to separate dissolved coal chemicals from mineral matter and insolubles (inertinite), resulting in the production of a purified hydrocarbon pitch. Alternatively, if hydrogenation is not used, aromatic hydrocarbon liquids appropriate for use as precursors to carbon products can obtained by dissolving coal in a solvent. As in the case for partial direct liquefaction pitches, undissolved coal is removed via hot filtration or centrifugation. Excess solvent is boiled off and recovered. The resultant solid material, referred to as Solvent Extracted Carbon Ore or SECO, has been used successfully to produce artificial graphite and carbon foam.

Chong Chen; Elliot B. Kennel; Liviu Magean; Pete G. Stansberry; Alfred H. Stiller; John W. Zondlo

2004-06-20T23:59:59.000Z

302

THE ECONOMICAL PRODUCTION OF ALCOHOL FUELS FROM COAL-DERIVED SYNTHESIS GAS  

DOE Green Energy (OSTI)

The kinetic data for a Mo-Ni-K/C catalyst were completed. Kinetic schemes were derived for the formation of methanol and ethanol over this catalyst. TPR results on alkali-substituted Mo/C are beginning to be amenable to a systematic quantitative analysis.

NONE

1997-04-01T23:59:59.000Z

303

REFORMULATION OF COAL-DERIVED TRANSPORTATION FUELS: SELECTIVE OXIDATION OF CARBON MONOXIDE ON METAL FOAM CATALYSTS  

DOE Green Energy (OSTI)

Several different catalytic reactions must be carried out in order to convert hydrocarbons (or alcohols) into hydrogen for use as a fuel for polyelectrolyte membrane (PEM) fuel cells. Each reaction in the fuel-processing sequence has a different set of characteristics, which influences the type of catalyst support that should be used for that particular reaction. A wide range of supports are being evaluated for the various reactions in the fuel-processing scheme, including porous and non-porous particles, ceramic and metal straight-channel monoliths, and ceramic and metal monolithic foams. These different types of support have distinctly different transport characteristics. The best choice of support for a given reaction will depend on the design constraints for the system, e.g., allowable pressure drop, and on the characteristics of the reaction for which the catalyst is being designed. Three of the most important reaction characteristics are the intrinsic reaction rate, the exothermicity/endothermicity of the reaction, and the nature of the reaction network, e.g., whether more than one reaction takes place and, in the case of multiple reactions, the configuration of the network. Isotopic transient kinetic analysis was used to study the surface intermediates. The preferential oxidation of low concentrations of carbon monoxide in the presence of high concentrations of hydrogen (PROX) is an important final step in most fuel processor designs. Data on the behavior of straight-channel monoliths and foam monolith supports will be presented to illustrate some of the factors involved in choosing a support for this reaction.

Mr. Paul Chin; Dr. Xiaolei Sun; Professor George W. Roberts; Professor James J. Spivey; Mr. Amornmart Sirijarhuphan; Dr. James G. Goodwin, Jr.; Dr. Richard W. Rice

2002-12-31T23:59:59.000Z

304

Integrated coal liquefaction process  

DOE Patents (OSTI)

In a process for the liquefaction of coal in which coal liquids containing phenols and other oxygenated compounds are produced during the liquefaction step and later hydrogenated, oxygenated compounds are removed from at least part of the coal liquids in the naphtha and gas oil boiling range prior to the hydrogenation step and employed as a feed stream for the manufacture of a synthesis gas or for other purposes.

Effron, Edward (Springfield, NJ)

1978-01-01T23:59:59.000Z

305

ANNUAL REPORT OCTOBER 1, 1979-SEPTEMBER 30, 1980 CHEMISTRY AND MORPHOLOGY OF COAL LIQUEFACTION  

E-Print Network (OSTI)

AND MORPHOLOGY OF COAL LIQUEFACTION LA , . . ,:;. ~~Microscope Studies of Coal during Hydrogenation Taskspread evenly over the coal grains of this particular area.

Heinemann, Heinz

2013-01-01T23:59:59.000Z

306

Coal Ash Behavior in Reducing Environments (CABRE) III Year 6 - Activity 1.10 - Development of a National Center for Hydrogen  

SciTech Connect

The Energy & Environmental Research Center (EERC) has been conducting research on gasification for six decades. One of the objectives of this gasification research has been to maximize carbon conversion and the watergas shift process for optimal hydrogen production and syngas quality. This research focus and experience were a perfect fit for the National Center for Hydrogen Technology (NCHT) Program at the EERC for improving all aspects of coal gasification, which ultimately aids in the production and purification of hydrogen. A consortia project was developed under the NCHT Program to develop an improved predictive model for ash formation and deposition under the project entitled Coal Ash Behavior in Reducing Environments (CABRE) III: Development of the CABRE III Model. The computer-based program is now applicable to the modeling of coal and ash behavior in both entrained-flow and fluidized-bed gasification systems to aid in overall gasification efficiency. This model represents a significant improvement over the CABRE II model and runs on a Microsoft Windows PC platform. The major achievements of the CABRE III model are partitioning of inorganic transformations between various phases for specific gas cleanup equipment; slag property predictions, including standard temperatureviscosity curves and slag flow and thickness; deposition rates in gasification cleanup equipment; provision for composition analysis for all input and output streams across all process equipment, including major elements and trace elements of interest; composition analysis of deposit streams for various deposit zones, including direct condensation on equipment surfaces (Zone A), homogeneous particulate deposition (Zone B), and entrained fly ash deposition (Zone C); and physical removal of ash in cyclones based on D50 cut points. Another new feature of the CABRE III model is a user-friendly interface and detailed reports that are easily exportable into Word documents, Excel spreadsheets, or as pdf files. The user interface provides stepwise guides with built-in checks for efficient entry of required input data on fuels of interest to allow a successful execution of the model. The model was developed with data from several fuels selected by the sponsors, including bituminous coal, subbituminous coal, lignite, and petroleum coke (petcoke). The data from these fuels were obtained using small pilot-scale entrained-flow and fluidized-bed gasifiers at the Energy & Environmental Research Center (EERC). The CABRE III model is expected to further advance the knowledge base for the NCHT Program and, more importantly, allow for prediction of the slagging and fouling characteristics of fuels in reducing environments. The information obtained from this program will potentially also assist in maintaining prolonged gasifier operation free from failure or facilitate troubleshooting to minimize downtime in the event of a problem.

Stanislowski, Joshua; Azenkeng, Alexander; McCollor, Donald; Galbreath, Kevin; Jensen, Robert; Lahr, Brent

2012-03-31T23:59:59.000Z

307

Coal liquefaction process streams characterization and evaluation. Characterization of coal-derived materials by field desorption mass spectrometry, two-dimensional nuclear magnetic resonance, supercritical fluid extraction, and supercritical fluid chromatography/mass spectrometry  

SciTech Connect

Under contract from the DOE , and in association with CONSOL Inc., Battelle, Pacific Northwest Laboratory (PNL) evaluated four principal and several complementary techniques for the analysis of non-distillable direct coal liquefaction materials in support of process development. Field desorption mass spectrometry (FDMS) and nuclear magnetic resonance (NMR) spectroscopic methods were examined for potential usefulness as techniques to elucidate the chemical structure of residual (nondistillable) direct coal liquefaction derived materials. Supercritical fluid extraction (SFE) and supercritical fluid chromatography/mass spectrometry (SFC/MS) were evaluated for effectiveness in compound-class separation and identification of residual materials. Liquid chromatography (including microcolumn) separation techniques, gas chromatography/mass spectrometry (GC/MS), mass spectrometry/mass spectrometry (MS/MS), and GC/Fourier transform infrared (FTIR) spectroscopy methods were applied to supercritical fluid extracts. The full report authored by the PNL researchers is presented here. The following assessment briefly highlights the major findings of the project, and evaluates the potential of the methods for application to coal liquefaction materials. These results will be incorporated by CONSOL into a general overview of the application of novel analytical techniques to coal-derived materials at the conclusion of CONSOL`s contract.

Campbell, J.A.; Linehan, J.C.; Robins, W.H. [Battelle Pacific Northwest Lab., Richland, WA (United States)

1992-07-01T23:59:59.000Z

308

DOE Hydrogen Analysis Repository: MiniCAM  

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

Oil, Gas, Biomass, Hydro, Nuclear, Wind, Solar PV), Hydrogen production (Coal, Oil, Gas, Biomass, Electrolysis), synthetic fuels (liquids and gases from coal, oil, gas,...

309

An Integrated Hydrogen Vision for California  

E-Print Network (OSTI)

of $2.00-2.50 per kilogram. Gasification of Coal and Othermore generally as gasification, hydrogen can be producedproduced from coal gasification POx processes at delivered

2004-01-01T23:59:59.000Z

310

Hydrogen Delivery Infrastructure Option Analysis  

E-Print Network (OSTI)

, vehicles can still drive with gasoline/diesel derived from tar sand, oil shale, and coal derived liquids

311

Determination of the Effect of Coal/Biomass-Derived Syngas Contaminants on the Performance of Fischer-Tropsch and Water-Gas-Shift Catalysts  

SciTech Connect

Today, nearly all liquid fuels and commodity chemicals are produced from non-renewable resources such as crude oil and natural gas. Because of increasing scrutiny of carbon dioxide (CO{sub 2}) emissions produced using traditional fossil-fuel resources, the utilization of alternative feedstocks for the production of power, hydrogen, value-added chemicals, and high-quality hydrocarbon fuels such as diesel and substitute natural gas (SNG) is critical to meeting the rapidly growing energy needs of modern society. Coal and biomass are particularly attractive as alternative feedstocks because of the abundant reserves of these resources worldwide. The strategy of co-gasification of coal/biomass (CB) mixtures to produce syngas for synthesis of Fischer-Tropsch (FT) fuels offers distinct advantages over gasification of either coal or biomass alone. Co-feeding coal with biomass offers the opportunity to exploit economies of scale that are difficult to achieve in biomass gasification, while the addition of biomass to the coal gasifier feed leverages proven coal gasification technology and allows CO{sub 2} credit benefits. Syngas generated from CB mixtures will have a unique contaminant composition because coal and biomass possess different concentrations and types of contaminants, and the final syngas composition is also strongly influenced by the gasification technology used. Syngas cleanup for gasification of CB mixtures will need to address this unique contaminant composition to support downstream processing and equipment. To investigate the impact of CB gasification on the production of transportation fuels by FT synthesis, RTI International conducted thermodynamic studies to identify trace contaminants that will react with water-gas-shift and FT catalysts and built several automated microreactor systems to investigate the effect of single components and the synergistic effects of multiple contaminants on water-gas-shift and FT catalyst performance. The contaminants investigated were sodium chloride (NaCl), potassium chloride (KCl), hydrogen sulfide (H{sub 2}S), carbonyl sulfide (COS), ammonia (NH{sub 3}), and combinations thereof. This report details the thermodynamic studies and the individual and multi-contaminant results from this testing program.

Trembly, Jason; Cooper, Matthew; Farmer, Justin; Turk, Brian; Gupta, Raghubir

2010-12-31T23:59:59.000Z

312

Equation-of-state for fluids at high densities-hydrogen isotope measurements and thermodynamic derivations  

DOE Green Energy (OSTI)

Hydrogen isotopes play an important role in energy technologies, in particular, the compression to high densities for initiation of controlled thermonuclear fusion energy. At high densities the properties of the compressed hydrogen isotopes depart drastically from ideal thermodynamic predictions. The measurement of accurate data including the author's own recent measurements of n-H/sub 2/ and n-D/sub 2/ in the range 75 to 300 K and 0.2 to 2.0 GPa (2 to 20 kbar) is reviewed. An equation-of-state of the Benedict type is fit to these data with a double-process least-squares computer program. The results are reviewed and compared with existing data and with a variety of theoretical work reported for fluid hydrogens. A new heuristic correlation is presented for simplicity in predicting volumes and sound velocity at high pressures. 9 figures, 1 table.

Liebenberg, D.H.; Mills, R.L.; Bronson, J.C.

1977-01-01T23:59:59.000Z

313

Prediction of thermodynamic properties of coal derivatives. Annual technical report, March 1, 1992--February 28, 1993  

Science Conference Proceedings (OSTI)

The purpose of this research program is to understand and model the effect of the different intermolecular forces on the thermodynamic properties of systems containing pure compounds and mixtures. The compounds under consideration vary considerably in size, shape and energy. Therefore in order to develop a theory capable of describing accurately the thermodynamic properties and phase behavior of such systems over a wide range of temperature and pressure, one has to take into account explicitly the differences in shape and size among the various compounds as well as the different type of intermolecular interactions. We have developed equations of state for pure-component chain molecules. We have shown that the excellent performance of complicated theories such as the Generalized Flory Dimer (GFD) theory can be mimicked by simpler equations, if certain assumptions for the shape parameters are made. We developed engineering correlations based on the GFD theory, using local composition theory to take into account the attractive contribution. We compared various methods for the calculation of the repulsive and attractive contributions against computer simulation data for hard and square-well chains, and experimental data from the literature. We also have studied microstructure and local order in fluids that contain asymmetric molecules. In addition, simple cubic equations of state have been applied to calculate physical and chemical-reaction equilibria in non-ideal systems. In order to obtain a better understanding of the intermolecular forces and to test some of our recent models, we have performed considerable experimental work. We used FT-IR to examine the self-association of aliphatic alcohols due to hydrogen bonding. In addition, FT-IR spectroscopy was used to investigate Lewis acid-base interactions between probe and entrainer-cosolvent molecules.

Donohue, M.D.

1992-11-01T23:59:59.000Z

314

THE ECONOMICAL PRODUCTION OF ALCOHOL FUELS FROM COAL-DERIVED SYNTHESIS GAS  

DOE Green Energy (OSTI)

Langmuir-Hinshelwood-type kinetic schemes were derived for the formation of methanol through butanol and total hydrocarbons over a Co-K-MoS{sub 2}/C catalyst. Reduced Mo-Ni-K/C materials continue to be considered as promising catalysts for HAS. A kinetic study of this catalyst has been started. TPR results on alkali-substituted Mo/C are beginning to be amenable to a systematic quantitative analysis. The characterization studies of transition-metal-oxide catalysts has ended. Consideration of various models for the performance of a packed-bed membrane reactor in the synthesis of methanol indicates that a model involving large (but finite) permeances of CO and MeOH may be optimal. Comparison of the membrane reactor with a packed-bed tubular reactor indicates that the former may be advantageous at low total flow rates.

NONE

1997-01-01T23:59:59.000Z

315

Microsoft Word - FE_Hydrogen_Program_Plan_2003_External_FINAL...  

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

OFFICE OF FOSSIL ENERGY - HYDROGEN PROGRAM PLAN HYDROGEN COORDINATION GROUP JUNE 2003 Hydrogen from Natural Gas and Coal: The Road to a Sustainable Energy Future HYDROGEN FROM...

316

Bioconversion of coal derived synthesis gas to liquid fuels. Quarterly technical progress report, 1 April--30 June 1994  

DOE Green Energy (OSTI)

The overall objective of the project is to develop an integrated two-stage fermentation process for conversion of coal-derived synthesis gas to a mixture of alcohols. This is achieved in two steps. In the first step, Butyribacterium methylotrophicum converts carbon monoxide (CO) to butyric and acetic acids. Subsequent fermentation of the acids by Clostridium acetobutylicum leads to the production of butanol and ethanol. The tasks for this quarter were: development/isolation of superior strains for fermentation of syngas; evaluation of bioreactor configuration for improved mass transfer of syngas; recovery of carbon and electrons from H{sub 2}-CO{sub 2}; initiation of pervaporation for recovery of solvents; and selection of solid support material for trickle-bed fermentation. Technical progress included the following. Butyrate production was enhanced during H{sub 2}/CO{sub 2} (50/50) batch fermentation. Isolation of CO-utilizing anaerobic strains is in progress. Pressure (15 psig) fermentation was evaluated as a means of increasing CO availability. Polyurethane foam packing material was selected for trickle bed solid support. Cell recycle fermentation on syngas operated for 3 months. Acetate was the primary product at pH 6.8. Trickle bed and gas lift fermentor designs were modified after initial water testing. Pervaporation system was constructed. No alcohol selectivity was shown with the existing membranes during initial start-up.

Jain, M.K.; Worden, R.M.; Grethlein, A.

1994-07-18T23:59:59.000Z

317

Co-firing high sulfur coal with refuse derived fuels. Technical progress report No. 5, [October--December 1995  

DOE Green Energy (OSTI)

Studies involving the tubular furnace are in the process of identifying the ideal experimental coal-to-refuse derived fuel(RDF) ratio for use in the AFBC system. A series of experiments with this furnace has been performed to determine the possible chemical pathway for formation of chlorinated organic compounds during the combustion of various RDF sources. Phenol and chlorine appear to be likely reactants necessary for the formation of these compounds. The main goal of these experiment is to determine the exact experimental conditions for the formation of chlorinated organic compounds, as well as methods to inhibit their development. Work on the fluidized bed combustor has involved five combustion runs, in which a combustion efficiency of greater than 96% and with a consistent CO{sub 2} concentration of approximately 13% was obtained. Modifications responsible for these improvements include the addition of the underbed fuel feed system and revision of the flue gas sampling system. New methods of determining combustion efficiency and percentage of SO{sub 2} capture using TG techniques to analyze combustion products are being developed. The current outlook using this TGA/FTIR method is very promising, since previously obscured reactions are being studied. the analysis of combustion products is revealing a more complete picture of the combustion process within the AFBC system.

Pan, Wei-Ping; Riley, J.T.; Lloyd, W.G.

1995-11-30T23:59:59.000Z

318

Upgraded Coal Interest Group  

Science Conference Proceedings (OSTI)

The Upgraded Coal Interest Group (UCIG) is an EPRI 'users group' that focuses on clean, low-cost options for coal-based power generation. The UCIG covers topics that involve (1) pre-combustion processes, (2) co-firing systems and fuels, and (3) reburn using coal-derived or biomass-derived fuels. The UCIG mission is to preserve and expand the economic use of coal for energy. By reducing the fuel costs and environmental impacts of coal-fired power generation, existing units become more cost effective and thus new units utilizing advanced combustion technologies are more likely to be coal-fired.

Evan Hughes

2009-01-08T23:59:59.000Z

319

A GIS-based Assessment of Coal-based Hydrogen Infrastructure Deployment in the State of Ohio  

E-Print Network (OSTI)

2004. [12] Parks K. GIS-based infrastructure modeling, 2010information systems (GIS). Washington, DC: National Hydrogenwww.elsevier.com/locate/he A GIS-based assessment of coal-

Johnson, Nils; Yang, Christopher; Ogden, J

2009-01-01T23:59:59.000Z

320

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

Note: This page contains sample records for the topic "hydrogen coal derived" 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

TECHNICAL AND ECONOMIC ASSESSMENT OF TRANSITION STRATEGIES TOWARD WIDESPREAD USE OF HYDROGEN AS AN ENERGY CARRIER  

E-Print Network (OSTI)

of hydrogen from: Coal gasification with and without CO 22 sequestration Biomass gasification Distributed productionof hydrogen from: Coal gasification with and without CO 2

Ogden, J; Yang, Christopher; Johnson, Nils; Ni, Jason; Lin, Zhenhong

2005-01-01T23:59:59.000Z

322

Technical and Economic Assessment of Transition Strategies Toward Widespread Use of Hydrogen as an Energy Carrier  

E-Print Network (OSTI)

of hydrogen from: Coal gasification with and without CO 22 sequestration Biomass gasification Distributed productionof hydrogen from: Coal gasification with and without CO 2

Ogden, Joan M; Yang, Christopher; Johnson, Nils; Ni, Jason; Lin, Zhenhong

2005-01-01T23:59:59.000Z

323

DOE Hydrogen and Fuel Cells Program: 2011 Annual Progress Report  

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

1 1 Printable Version 2011 Annual Progress Report The 2011 Progress Report for the DOE Hydrogen and Fuel Cells Program summarizes the hydrogen and fuel cell R&D activities and accomplishments for FY 2011. Published in November 2011, the full document is very large; each technical report is available as an individual Adobe Acrobat PDF. Front Cover and Title Page Table of Contents I. Introduction, Sunita Satyapal, U.S. Department of Energy II. Hydrogen Production Distributed Bio-Derived Liquid Production Biomass Gasification Separations Hydrogen from Coal Electrolysis Hi-Temp Thermochemical Photoelectrochemical Biological Production Analysis Production Basic Energy Sciences III. Hydrogen Delivery IV. Hydrogen Storage Metal Hydride Chemical Hydrogen Storage Hydrogen Sorption

324

DOE Hydrogen and Fuel Cells Program: 2010 Annual Progress Report  

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

0 0 Printable Version 2010 Annual Progress Report The 2010 Progress Report for the DOE Hydrogen Program summarizes the hydrogen and fuel cell R&D activities and accomplishments for FY 2010. Published in February 2011, the full document is very large; each technical report is available as an individual Adobe Acrobat PDF. Front Cover Table of Contents I. Introduction, Sunita Satyapal, U.S. Department of Energy II. Hydrogen Production Distributed Bio-Derived Liquid Production Biomass Gasification Separations Hydrogen from Coal Electrolysis Hi-Temp Thermochemical Photoelectrochemical Biological Production Cross-Cutting/Production III. Hydrogen Delivery IV. Hydrogen Storage Metal Hydride Center of Excellence Chemical Hydrogen Storage Center of Excellence Hydrogen Sorption Center of Excellence

325

Degradation of SOFC anodes and SOFC performance in coal ...  

Science Conference Proceedings (OSTI)

Symposium, Materials in Clean Power Systems V: Clean Coal-, Hydrogen ... of SOFC anodes and SOFC performance in coal syngas containing phosphine.

326

Proceedings, twenty-five annual international Pittsburgh coal conference  

SciTech Connect

The conference theme was 'coal - energy, environment and sustainable development'. The topics covered energy and environmental issues, and technologies related to coal and its byproducts. These included: gasification, hydrogen from coal, combustion technologies, coal production and preparation, synthesis of liquid fuels, gas turbines and fuel cells for synthesis gas and hydrogen applications, coal chemistry and geosciences, global climate change, underground coal gasification, environmental control technologies, and coal utilization byproducts.

NONE

2008-07-01T23:59:59.000Z

327

DOE Hydrogen Analysis Repository: Infrastructure Costs Associated...  

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

Infrastructure Costs Associated with Central Hydrogen Production from Biomass and Coal Project Summary Full Title: Infrastructure Costs Associated with Central Hydrogen Production...

328

New Projects Set to Target Efficiency, Environmental Gains at Advanced Coal  

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

Projects Set to Target Efficiency, Environmental Gains at Projects Set to Target Efficiency, Environmental Gains at Advanced Coal Gasification Facilities New Projects Set to Target Efficiency, Environmental Gains at Advanced Coal Gasification Facilities July 27, 2010 - 1:00pm Addthis Washington, D.C. -- Four projects that will demonstrate an innovative technology that could eventually enhance hydrogen fuel production, lower greenhouse gas (GHG) emissions, improve efficiencies and lower consumer electricity costs from advanced coal gasification power systems have been selected by the U.S. Department of Energy (DOE). The projects will test membrane technology to separate hydrogen and carbon dioxide (CO2) from coal or coal/biomass-derived synthesis gas (syngas), such as from Integrated Gasification Combined Cycle (IGCC) power systems.

329

Basic properties of coals and other solids. Final report, September 1, 1989--August 30, 1992  

SciTech Connect

The previous project dissected the heats of interactions of a series of coals into components that represented Bronsted acidity, hydrogen-bonding acidity and dispersion force interactions through comparison with the simple prototype solid acids: sulfonic acid resin, silica, and graphitized carbon black respectively. The present grant has emphasized the interaction of basic components in the coal with strong Bronsted acids and boron trichloride, a very strong Lewis acid, with a brief examination of the interactions of the coals with phenols as weaker hydrogen-bonding acids. We have also compared several coals with liquids derived from them at Wilsonville and Exxon. Finally, we have examined the effect of citric acid washing on several coals.

Arnett, E.M.

1992-12-31T23:59:59.000Z

330

Rough cost estimates of solar thermal/coal or biomass-derived fuels. [Hybrid approach: solar thermal plus either coal or biomass  

SciTech Connect

The production of a synthetic fuel from a solar thermal resource could provide a means of replacing critical liquid and gaseous fossil fuels. The solar thermal resource is large and economics favors a southwestern site. A synthetic fuel would provide a desirable product and a means of transporting solar thermal energy to large load centers outside the southwest. This paper presents cost data for one method of producing synthetic methane. A hybrid approach was chosen, a combination of solar thermal and either coal or biomass. The magnitude of the solar thermal resource is estimated as well as projected cost. Cost projections for coal and biomass are accumulated. The cost of synthetic gas from a hybrid and a conventional fuel source are compared.

Copeland, R. J.

1979-01-01T23:59:59.000Z

331

Hydrogen Storage Using Electric Field Enhanced Adsorption  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2010 TMS Annual Meeting & Exhibition. Symposium , Materials in Clean Power Systems V: Clean Coal-, Hydrogen...

332

NATIONAL HYDROGEN ENERGY ROADMAP  

E-Print Network (OSTI)

and replaced by coal gasification with carbon sequestration and, to a lesser extent, by biomass gasification. By 2050, biomass and wind, combined, provide 35% of hydrogen supplies. Hydrogen production from nuclear.energy.gov/hydrogenandfuelcells/posture_plan04.html. sequestration sites opt for more coal gasification while those with ample wind or biomass

333

Study of hydrogen in coals, polymers, oxides, and muscle water by nuclear magnetic resonance; extension of solid-state high-resolution techniques. [Hydrogen molybdenum bronze  

DOE Green Energy (OSTI)

Nuclear magnetic resonance (NMR) spectroscopy has been an important analytical and physical research tool for several decades. One area of NMR which has undergone considerable development in recent years is high resolution NMR of solids. In particular, high resolution solid state /sup 13/C NMR spectra exhibiting features similar to those observed in liquids are currently achievable using sophisticated pulse techniques. The work described in this thesis develops analogous methods for high resolution /sup 1/H NMR of rigid solids. Applications include characterization of hydrogen aromaticities in fossil fuels, and studies of hydrogen in oxides and bound water in muscle.

Ryan, L.M.

1981-10-01T23:59:59.000Z

334

Program on Technology Innovation: Wavelength-Multiplexed Diode Laser Absorption Sensors for Rapid Monitoring of Coal-Derived Synthesis Gas  

Science Conference Proceedings (OSTI)

Sensors are needed to monitor gas temperature and synthesis products during coal gasificationin the reactor, at the reactor exit, and along the path to potential use by gas turbines. The harsh operating conditions of coal gasification create a challenging measurement environment. In particular, an optimized gasifier is operated at pressures of 2040 atm (20274053 kPa) with the expectation for operation at even higher pressures. The synthesis gas is also heavily laden with particulate, and the gasifier r...

2012-02-27T23:59:59.000Z

335

Proceedings, twenty-fourth annual international Pittsburgh coal conference  

SciTech Connect

Topics covered include: gasification technologies; coal production and preparation; combustion technologies; environmental control technologies; synthesis of liquid fuels, chemicals, materials and other non-fuel uses of coal; hydrogen from coal; advanced synthesis gas cleanup; coal chemistry, geosciences and resources; Fischer-Tropsch technology; coal and sustainability; global climate change; gasification (including underground gasification); materials, instrumentation and controls; and coal utilisation byproducts.

NONE

2007-07-01T23:59:59.000Z

336

HS_Coal_Studyguide.indd  

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

Coal Coal Fossil Energy Study Guide: Coal Coal is the most plentiful fuel in the fossil family. The United States has more coal reserves than any other country in the world. In fact, one-fourth of all known coal in the world is in the United States, with large deposits located in 38 states. The United States has almost as much energ y in coal that can be mined as the rest of the world has in oil that can be pumped from the ground. TYPES OF COAL Coal is a black rock made up of large amounts of carbon. Like all fossil fuels, coal can be burned to release energy. Coal contains elements such as hydrogen, oxygen, and nitrogen; has various amounts of minerals; and is itself considered to be a mineral of organic origin. Due to the variety of materials buried over time in the

337

HYDROGENATION AND CRACKING OF COAL RELATED FUSED-RING STRUCTURES USING ZnCl2 AND AlCl3 CATALYSTS  

E-Print Network (OSTI)

The Na enes in Processed Coal EPRI Report AF- & DevelopmentCA (1976). Whitehurst, Coals in Behavior of Western at EPRIH. H. , ed. , Chemistry of Coal Utilization~~_:e.l~mer:

Salim, Sadie S.

2013-01-01T23:59:59.000Z

338

EFFECTS OF LEWIS ACID CATALYSTS ON THE HYDROGENATION AND CRACKING OF TWO-RING AROMATIC AND HYDROAROMATIC STRUCTURES RELATED TO COAL  

E-Print Network (OSTI)

Asphaltenes in Processed Coal", EPRI Report AF-480, preparedS. A. and Bell, A. T. , "Coal Liquefaction Using ZincJ. H. , and Vermeulen, T. , "Coal Conversion Using Zinc

Salim, Sadie S.

2013-01-01T23:59:59.000Z

339

Production of low-cost hydrogen. Final report, September 1989--August 1993  

DOE Green Energy (OSTI)

Significant technical progress has been made over the last decade to develop efficient processes for upgrading coal resources to distillable hydrocarbons which may be used to displace petroleum-derived fuels. While several different direct coal liquefaction routes are under investigation, each of them have in common the need for large quantities of hydrogen to convert the aromatic coal matrix to liquid products in the normal distillation range, and for hydrotreating to improve liquid product quality. In fact, it has been estimated that the production, recovery, and efficient use of hydrogen accounts for over 50 percent of the capital cost of the liquefaction facility. For this reason, improved methods for producing low-cost hydrogen are essential to the operating economics of the liquefaction process. This Final Report provides an assessment of the application of the MTCI indirect gasification technology for the production of low-cost hydrogen from coal feedstocks. The MTCI gasification technology is unique in that it overcomes many of the problems and issues associated with direct and other indirectly heated coal gasification systems. Although the MTCI technology can be utilized for producing hydrogen from almost any carbonaceous feedstock (fossil, biomass and waste), this report presents the results of an experimental program sponsored by the Department of Energy, Morgantown Energy Research Center, to demonstrate the production of hydrogen from coal, mild gasification chars, and liquefaction bottoms.

Not Available

1993-06-01T23:59:59.000Z

340

Integrated coal cleaning, liquefaction, and gasification process  

DOE Patents (OSTI)

Coal is finely ground and cleaned so as to preferentially remove denser ash-containing particles along with some coal. The resulting cleaned coal portion having reduced ash content is then fed to a coal hydrogenation system for the production of desirable hydrocarbon gases and liquid products. The remaining ash-enriched coal portion is gasified to produce a synthesis gas, the ash is removed from the gasifier usually as slag, and the synthesis gas is shift converted with steam and purified to produce the high purity hydrogen needed in the coal hydrogenation system. This overall process increases the utilization of as-mined coal, reduces the problems associated with ash in the liquefaction-hydrogenation system, and permits a desirable simplification of a liquids-solids separation step otherwise required in the coal hydrogenation system.

Chervenak, Michael C. (Pennington, NJ)

1980-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

Method for coal liquefaction  

DOE Patents (OSTI)

A process is disclosed for coal liquefaction in which minute particles of coal in intimate contact with a hydrogenation catalyst and hydrogen arc reacted for a very short time at a temperature in excess of 400 C at a pressure of at least 1500 psi to yield over 50% liquids with a liquid to gaseous hydrocarbon ratio in excess of 8:1. 1 figures.

Wiser, W.H.; Oblad, A.G.; Shabtai, J.S.

1994-05-03T23:59:59.000Z

342

Coal liquefaction process  

DOE Patents (OSTI)

A C.sub.5 -900.degree. F. (C.sub.5 -482.degree. C.) liquid yield greater than 50 weight percent MAF feed coal is obtained in a coal liquefaction process wherein a selected combination of higher hydrogen partial pressure, longer slurry residence time and increased recycle ash content of the feed slurry are controlled within defined ranges.

Carr, Norman L. (Allison Park, PA); Moon, William G. (Cheswick, PA); Prudich, Michael E. (Pittsburgh, PA)

1983-01-01T23:59:59.000Z

343

Hydrogenation of carbonaceous materials  

DOE Patents (OSTI)

A method for reacting pulverized coal with heated hydrogen-rich gas to form hydrocarbon liquids suitable for conversion to fuels wherein the reaction involves injection of pulverized coal entrained in a minimum amount of gas and mixing the entrained coal at ambient temperature with a separate source of heated hydrogen. In accordance with the present invention, the hydrogen is heated by reacting a small portion of the hydrogen-rich gas with oxygen in a first reaction zone to form a gas stream having a temperature in excess of about 1000.degree. C. and comprising a major amount of hydrogen and a minor amount of water vapor. The coal particles then are reacted with the hydrogen in a second reaction zone downstream of the first reaction zone. The products of reaction may be rapidly quenched as they exit the second reaction zone and are subsequently collected.

Friedman, Joseph (Encino, CA); Oberg, Carl L. (Canoga Park, CA); Russell, Larry H. (Agoura, CA)

1980-01-01T23:59:59.000Z

344

DOE Hydrogen and Fuel Cells Program: 2009 Annual Progress Report  

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

9 9 Printable Version 2009 Annual Progress Report The 2009 Progress Report for the DOE Hydrogen Program summarizes the hydrogen and fuel cell R&D activities and accomplishments for FY 2009. Published in November 2009, the full document is very large; each technical report is available as an individual Adobe Acrobat PDF. Download Adobe Reader. Front Cover (PDF 1.2 MB) Table of Contents (PDF 318 KB) I. Introduction, Sunita Satyapal, U.S. Department of Energy (PDF 1.5 MB) II. Hydrogen Production Distributed Production from Bio-Derived Liquids Biomass Gasification Separations Hydrogen from Coal Electrolysis Hi-Temp Thermochemical Nuclear Hydrogen Initiative Photoelectrochemical Biological Cross-Cutting/Production III. Hydrogen Delivery IV. Hydrogen Storage Metal Hydride Center of Excellence

345

DOE Hydrogen and Fuel Cells Program: 2008 Annual Progress Report  

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

8 8 Printable Version 2008 Annual Progress Report The 2008 Progress Report for the DOE Hydrogen Program summarizes the hydrogen and fuel cell R&D activities and accomplishments for FY 2008. Published in November 2008, the full document is very large; each technical report is available as an individual Adobe Acrobat PDF. Download Adobe Reader. Front Cover (PDF 1.2 MB) Table of Contents (PDF 180 KB) I. Introduction, JoAnn Milliken, U.S. Department of Energy (PDF 980 KB) II. Hydrogen Production Distributed Production from Bio-Derived Liquids Electrolysis Separations Biomass Gasification Photoelectrochemical Biological Production Hydrogen From Coal Nuclear Hydrogen Initiative Hi-Temp Thermochemical Cross-Cutting Basic Energy Sciences III. Hydrogen Delivery IV. Hydrogen Storage

346

CATALYTIC CONVERSION OF SOLVENT REFINED COAL TO LIQUID PRODUCTS  

E-Print Network (OSTI)

I. Solvent Refined Coal II. Catalysts III. Purpose andSondreal, E.A. , "Viscosity of Coal Liquids - The Effect ofAnthraxylon - Kinetics of Coal Hydrogenation," Ind. and Eng.

Tanner, K.I.

2010-01-01T23:59:59.000Z

347

Process to upgrade coal liquids by extraction prior to hydrodenitrogenation  

DOE Patents (OSTI)

Oxygen compounds are removed, e.g., by extraction, from a coal liquid prior to its hydrogenation. As a result, compared to hydrogenation of such a non-treated coal liquid, the rate of nitrogen removal is increased.

Schneider, Abraham (Overbrook Hills, PA); Hollstein, Elmer J. (Wilmington, DE); Janoski, Edward J. (Havertown, PA); Scheibel, Edward G. (Media, PA)

1982-01-01T23:59:59.000Z

348

System Study of Rich Catalytic/Lean burn (RCL) Catalytic Combustion for Natural Gas and Coal-Derived Syngas Combustion Turbines  

SciTech Connect

Rich Catalytic/Lean burn (RCL{reg_sign}) technology has been successfully developed to provide improvement in Dry Low Emission gas turbine technology for coal derived syngas and natural gas delivering near zero NOx emissions, improved efficiency, extending component lifetime and the ability to have fuel flexibility. The present report shows substantial net cost saving using RCL{reg_sign} technology as compared to other technologies both for new and retrofit applications, thus eliminating the need for Selective Catalytic Reduction (SCR) in combined or simple cycle for Integrated Gasification Combined Cycle (IGCC) and natural gas fired combustion turbines.

Shahrokh Etemad; Lance Smith; Kevin Burns

2004-12-01T23:59:59.000Z

349

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

Science Conference Proceedings (OSTI)

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

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

2006-05-15T23:59:59.000Z

350

DESIGNING AND OPPORTUNITY FUEL WITH BIOMASS AND TIRE-DERIVED FUEL FOR COFIRING AT WILLOW ISLAND GENERATING STATION AND COFIRING SAWDUST WITH COAL AT ALBRIGHT GENERATING STATION  

DOE Green Energy (OSTI)

During the period July 1, 2000-March 31, 2004, Allegheny Energy Supply Co., LLC (Allegheny) conducted an extensive demonstration of woody biomass cofiring at its Willow Island and Albright Generating Stations. This demonstration, cofunded by USDOE and Allegheny, and supported by the Biomass Interest Group (BIG) of EPRI, evaluated the impacts of sawdust cofiring in both cyclone boilers and tangentially-fired pulverized coal boilers. The cofiring in the cyclone boiler--Willow Island Generating Station Unit No.2--evaluated the impacts of sawdust alone, and sawdust blended with tire-derived fuel. The biomass was blended with the coal on its way to the combustion system. The cofiring in the pulverized coal boiler--Albright Generating Station--evaluated the impact of cofiring on emissions of oxides of nitrogen (NO{sub x}) when the sawdust was injected separately into the furnace. The demonstration of woody biomass cofiring involved design, construction, and testing at each site. The results addressed impacts associated with operational issues--capacity, efficiency, and operability--as well as formation and control of airborne emissions such as NO{sub x}, sulfur dioxide (SO{sub 2}2), opacity, and mercury. The results of this extensive program are detailed in this report.

K. Payette; D. Tillman

2004-06-01T23:59:59.000Z

351

Low-rank coal oil agglomeration  

DOE Patents (OSTI)

A low-rank coal oil agglomeration process. High mineral content, a high ash content subbituminous coals are effectively agglomerated with a bridging oil which is partially water soluble and capable of entering the pore structure, and usually coal derived.

Knudson, Curtis L. (Grand Forks, ND); Timpe, Ronald C. (Grand Forks, ND)

1991-01-01T23:59:59.000Z

352

Combustion-Turbine Design Guidelines Based on Deposition-Corrosion Considerations, Volume 2: Coal-Derived Liquid Studies  

Science Conference Proceedings (OSTI)

Middle-distillate coal liquids test out as acceptable gas turbine fuels in terms of deposition and corrosion. Solid-liquid slurries would also be acceptable if turbine cleaning techniques were fully used.This series of tests provided design and operating guidelines that would minimize ash deposition and turbine corrosion.

1984-06-01T23:59:59.000Z

353

Low temperature aqueous desulfurization of coal  

DOE Patents (OSTI)

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

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

1985-01-01T23:59:59.000Z

354

Low temperature aqueous desulfurization of coal  

DOE Patents (OSTI)

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

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

1985-04-18T23:59:59.000Z

355

Development and Implementation of Materials to Enable Clean Coal ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2010 TMS Annual Meeting & Exhibition. Symposium , Materials in Clean Power Systems V: Clean Coal-, Hydrogen...

356

The economical production of alcohol fuels from coal-derived synthesis gas: Case studies, design, and economics  

DOE Green Energy (OSTI)

This project is a combination of process simulation and catalyst development aimed at identifying the most economical method for converting coal to syngas to linear higher alcohols to be used as oxygenated fuel additives. There are two tasks. The goal of Task 1 is to discover, study, and evaluate novel heterogeneous catalytic systems for the production of oxygenated fuel enhancers from synthesis gas, and to explore, analytically and on the bench scale, novel reactor and process concepts for use in converting syngas to liquid fuel products. The goal of Task 2 is to simulate, by computer, energy efficient and economically efficient processes for converting coal to energy (fuel alcohols and/or power). The primary focus is to convert syngas to fuel alcohols. This report contains results from Task 2. The first step for Task 2 was to develop computer simulations of alternative coal to syngas to linear higher alcohol processes, to evaluate and compare the economics and energy efficiency of these alternative processes, and to make a preliminary determination as to the most attractive process configuration. A benefit of this approach is that simulations will be debugged and available for use when Task 1 results are available. Seven cases were developed using different gasifier technologies, different methods for altering the H{sub 2}/CO ratio of the syngas to the desired 1.1/1, and with the higher alcohol fuel additives as primary products and as by-products of a power generation facility. Texaco, Shell, and Lurgi gasifier designs were used to test gasifying coal. Steam reforming of natural gas, sour gas shift conversion, or pressure swing adsorption were used to alter the H{sub 2}/CO ratio of the syngas. In addition, a case using only natural gas was prepared to compare coal and natural gas as a source of syngas.

NONE

1995-10-01T23:59:59.000Z

357

COST-EFFECTIVE METHOD FOR PRODUCING SELF SUPPORTED PALLADIUM ALLOY MEMBRANES FOR USE IN EFFICIENT PRODUCTION OF COAL DERIVED HYDROGEN  

DOE Green Energy (OSTI)

In the past quarter, we have conducted additional characterization and permeation tests on different Pd alloy membranes including PdCuTa ternary alloy materials. We attempted to address some discrepancies between SwRI{reg_sign} and CSM relating to PdCu stoichiometry by preparing a range of PdCu membranes with compositions from {approx}58-65 at% Pd (bal. Cu). While some difficulties in cutting and sealing these thin membranes at CSM continue, some progress has been made in identifying improved membrane support materials. We have also completed an initial cost analysis for large-scale vacuum deposition and fabrication of thin Pd ally membranes and project that the process can meet DOE cost targets. Minimal progress was made in the past quarter relating to the testing of prototype membrane modules at Idatech. In the past quarter Idatech was acquired by a UK investment firm, which we believe may have impacted the ability of key technical personnel to devote sufficient time to support this effort. We are hopeful their work can be completed by the end of the calendar year.

J. Arps; K. Coulter

2006-09-30T23:59:59.000Z

358

Cost-Effective Method for Producing Self Supported Palladium Alloy Membranes for Use in Efficient Production of Coal Derived Hydrogen  

DOE Green Energy (OSTI)

In the past quarter, no technical work has been completed and a ''no cost'' time extension was requested and granted to allow IdaTech time to complete task 5 relating to the testing of prototype membrane modules. The scheduled completion date is now October 31, 2007.

K. Coulter

2007-03-31T23:59:59.000Z

359

Cost-Effective Method for Producing Self Supported Palladium Alloy Membranes for Use in Efficient Production of Coal Derived Hydrogen  

DOE Green Energy (OSTI)

Southwest Research Institute{reg_sign} (SwRI{reg_sign}) has utilized its expertise in large-area vacuum deposition methods to conduct research into the fabrication of dense, freestanding Pd-alloy membranes that are 3-5 microns thick and over 100 in{sup 2} in area. The membranes were deposited onto flexible and rigid supports that were subsequently removed and separated using novel techniques developed over the course of the project. Using these methods, the production of novel alloy compositions centered around the Pd-Cu system were developed with the objective of producing a thermally stable, nano-crystalline grain structure with the highest flux recorded as 242 SCFH/ft{sup 2} for a 2 {micro}m thick Pd{sub 53}Cu{sub 47} at 400 C and 20 psig feed pressure which when extrapolated is over twice the 2010 Department of Energy pure H{sub 2} flux target. Several membranes were made with the same permeability, but with different thicknesses and these membranes were highly selective. Researchers at the Colorado School of Mines supported the effort with extensive testing of experimental membranes as well as design and modeling of novel alloy composite structures. IdaTech provided commercial bench testing and analysis of SwRI-manufactured membranes. The completed deliverables for the project include test data on the performance of experimental membranes fabricated by vacuum deposition and several Pd-alloy membranes that were supplied to IdaTech for testing.

K. Coulter

2008-03-31T23:59:59.000Z

360

Cost-Effective Method for Producing Self Supported Palladium Alloy Membranes for Use in Efficient Production of Coal Derived Hydrogen  

DOE Green Energy (OSTI)

In the past quarter, no technical work has been completed and two ''no cost'' time extensions have been requested and granted to allow Idatech time to complete Task 5 relating to the testing of prototype membrane modules. The scheduled completion date of April 7, 2007 has been confirmed by Idatech.

K. Coulter

2006-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

COST-EFFECTIVE METHOD FOR PRODUCING SELF SUPPORTED PALLADIUM ALLOY MEMBRANES FOR USE IN EFFICIENT PRODUCTION OF COAL DERIVED HYDROGEN  

DOE Green Energy (OSTI)

Extending upon development efforts last quarter to produce ''free-standing'', copper and palladium alloy films, the goal this quarter has been to produce pinhole-free, Pd-Cu alloy films up to 5 x 5 inches in area (1-3 microns thick) using both magnetron sputtering and e-beam evaporation on PVA (Solublon) and polystyrene backing materials. A set of experiments were conducted to assess processing methods/solutions chemistry for removing the polymer backing material from the Pd-Cu film. For all of the alloy films produced to this point, we were unable to produce pinhole-free films on plastic although we were able to produce free-standing Pd-Cu films at less than 0.5 microns thick with minimal intrinsic stress. Subsequently, to evaluate gas permeation and leakage across the films, two films were sandwiched together on top of a porous Monel support disc (25 mm in diameter) and then tested in a leak test apparatus. Using two Cu films (10 micron thickness total) in the sandwich configuration, leak rates were about 20% of the background leak rate.

B. Lanning; J. Arps

2004-04-01T23:59:59.000Z

362

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

363

Coal liquefaction process  

DOE Patents (OSTI)

A process is described for the liquefaction of coal wherein raw feed coal is dissolved in recycle solvent with a slurry containing recycle coal minerals in the presence of added hydrogen at elevated temperature and pressure. The highest boiling distillable dissolved liquid fraction is obtained from a vacuum distillation zone and is entirely recycled to extinction. Lower boiling distillable dissolved liquid is removed in vapor phase from the dissolver zone and passed without purification and essentially without reduction in pressure to a catalytic hydrogenation zone where it is converted to an essentially colorless liquid product boiling in the transportation fuel range. 1 fig.

Wright, C.H.

1986-02-11T23:59:59.000Z

364

Coal liquefaction process  

DOE Green Energy (OSTI)

A process for the liquefaction of coal wherein raw feed coal is dissolved in recycle solvent with a slurry containing recycle coal minerals in the presence of added hydrogen at elevated temperature and pressure. The highest boiling distillable dissolved liquid fraction is obtained from a vacuum distillation zone and is entirely recycled to extinction. Lower boiling distillable dissolved liquid is removed in vapor phase from the dissolver zone and passed without purification and essentially without reduction in pressure to a catalytic hydrogenation zone where it is converted to an essentially colorless liquid product boiling in the transportation fuel range.

Wright, Charles H. (Overland Park, KS)

1986-01-01T23:59:59.000Z

365

Why Hydrogen? Hydrogen from Diverse Domestic Resources  

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

& RELIABILITY ZERONEAR ZERO ZERONEAR ZERO EMISSIONS EMISSIONS Why Hydrogen? Biomass Hydro Wind Solar Coal Nuclear Natural Gas Oil S e q u e s t r a t i o n Biomass Hydro Wind...

366

Biomass-Derived Hydrogen from a Thermally Ballasted Gasifier Robert C. Brown, Glenn Norton, Andy Suby, Jerod Smeenk, Keith Cummer, and Josh Nunez  

E-Print Network (OSTI)

Biomass-Derived Hydrogen from a Thermally Ballasted Gasifier Robert C. Brown, Glenn Norton, Andy fuel cells. We have developed a thermally ballasted gasifier that uses a single reactor for both compared to conventional gasifiers. The carbon monoxide, along with steam used to fluidize the reactor, can

367

Catalytic coal hydroliquefaction process  

SciTech Connect

A process is described for the liquefaction of coal in a hydrogen donor solvent in the presence of hydrogen and a co-catalyst combination of iron and a Group VI or Group VIII non-ferrous metal or compounds of the catalysts.

Garg, Diwakar (Macungie, PA)

1984-01-01T23:59:59.000Z

368

Catalytic hydroprocessing of coal-derived gasification residues to fuel blending stocks: effect of reaction variables and catalyst on hydrodeoxygenation (HDO), hydrodenitrogenation (HDN), and hydrodesulfurization (HDS)  

SciTech Connect

Gas liquors, tar oils, and tar products resulting from the coal gasification of a high-temperature Fischer-Tropsch plant can be successfully refined to fuel blending components by the use of severe hydroprocessing conditions. High operating temperatures and pressures combined with low space velocities ensure the deep hydrogenation of refractory oxygen, sulfur, and nitrogen compounds. Hydrodeoxygenation, particularly the removal of phenolic components, hydrodesulfurization, and hydrodenitrogenation were obtained at greater than 99% levels using the NiMo and NiW on {gamma}-Al{sub 2}O{sub 3} catalysts. Maximum deoxygenation activity was achieved using the NiMo/{gamma}-Al{sub 2}O{sub 3} catalyst having a maximum pore size distribution in the range of 110-220{angstrom}. The NiMo/{gamma}-Al{sub 2}O{sub 3} catalyst, which also has a relatively high proportion of smaller pore sizes (35-60 {angstrom}), displays lower hydrogenation activity. 30 refs., 1 fig. 8 tabs.

Dieter Leckel [Sasol Technology Research and Development, Sasolburg (South Africa). Fischer-Tropsch Refinery Catalysis

2006-10-15T23:59:59.000Z

369

Hydrogen Fuel | Department of Energy  

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

14, 2013 - 2:06pm Addthis Hydrogen is a clean fuel that, when consumed, produces only water. Hydrogen can be produced from a variety of domestic sources, such as coal, natural...

370

Co-combustion of refuse derived fuel and coal in a cyclone furnace at the Baltimore Gas and Electric Company, C. P. Crane Station  

DOE Green Energy (OSTI)

A co-combustion demonstration burn of coal and fluff refuse-derived fuel (RDF) was conducted by Teledyne National and Baltimore Gas and Electric Company. This utility has two B and W cyclone furnaces capable of generating 400 MW. The facility is under a prohibition order to convert from No. 6 oil to coal; as a result, it was desirable to demonstrate that RDF, which has a low sulfur content, can be burned in combination with coals containing up to 2% sulfur, thus reducing overall sulfur emissions without deleterious effects. Each furnace consists of four cyclones capable of generating 1,360,000 pounds per hour steam. The tertiary air inlet of one of the cyclones was modified with an adapter to permit fluff RDF to be pneumatically blown into the cyclone. At the same time, coal was fed into the cyclone furnace through the normal coal feeding duct, where it entered the burning chamber tangentially and mixed with the RDF during the burning process. Secondary shredded fluff RDF was prepared by the Baltimore County Resource Recovery Facility. The RDF was discharged into a receiving station consisting of a belt conveyor discharging into a lump breaker, which in turn, fed the RDF into a pneumatic line through an air-lock feeder. A total of 2316 tons were burned at an average rate of 5.6 tons per hour. The average heat replacement by RDF for the cyclone was 25%, based on Btu input for a period of forty days. The range of RDF burned was from 3 to 10 tons per hour, or 7 to 63% heat replacement. The average analysis of the RDF (39 samples) for moisture, ash, heat (HHV) and sulfur content were 18.9%, 13.4%, 6296 Btu/lb and 0.26% respectively. RDF used in the test was secondary shredded through 1-1/2 inch grates producing the particle size distribution of from 2 inches to .187 inches. Findings to date after inspection of the boiler and superheater indicate satisfactory results with no deleterious effects from the RDF.

Not Available

1982-03-01T23:59:59.000Z

371

INTERACTION OF A SUB-BITUMINOUS COAL WITH A STRONG ACID AND A STRONG BASE  

E-Print Network (OSTI)

production coal-derived hydrocarbons. Coal is more easily recovered and more widely available than oil shale and

Seth, M.

2010-01-01T23:59:59.000Z

372

Catalytic two-stage coal liquefaction process having improved nitrogen removal  

SciTech Connect

A process for catalytic multi-stage hydrogenation and liquefaction of coal to produce high yields of low-boiling hydrocarbon liquids containing low concentrations of nitogen compounds. First stage catalytic reaction conditions are 700.degree.-800.degree. F. temperature, 1500-3500 psig hydrogen partial pressure, with the space velocity maintained in a critical range of 10-40 lb coal/hr ft.sup.3 catalyst settled volume. The first stage catalyst has 0.3-1.2 cc/gm total pore volume with at least 25% of the pore volume in pores having diameters of 200-2000 Angstroms. Second stage reaction conditions are 760.degree.-870.degree. F. temperature with space velocity exceeding that in the first stage reactor, so as to achieve increased hydrogenation yield of low-boiling hydrocarbon liquid products having at least 75% removal of nitrogen compounds from the coal-derived liquid products.

Comolli, Alfred G. (Yardley, PA)

1991-01-01T23:59:59.000Z

373

Oxidative decomposition of formaldehyde catalyzed by a bituminous coal  

Science Conference Proceedings (OSTI)

It has been observed that molecular hydrogen is formed during long-term storage of bituminous coals via oxidative decomposition of formaldehyde by coal surface peroxides. This study has investigated the effects of coal quantity, temperature, and water content on the molecular hydrogen formation with a typical American coal (Pittsburgh No. 6). The results indicate that the coal's surface serves as a catalyst in the formation processes of molecular hydrogen. Furthermore, the results also indicate that low temperature emission of molecular hydrogen may possibly be the cause of unexplained explosions in confined spaces containing bituminous coals, for example, underground mines or ship holds. 20 refs., 4 figs., 6 tabs.

Haim Cohen; Uri Green [Ariel University Center in Samaria, Beer Sheva (Israel). Biological Chemistry Department

2009-05-15T23:59:59.000Z

374

International Partnership for a Hydrogen Economy  

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

Partnership Partnership for the Hydrogen Economy (IPHE) U.S. Department of Energy Why Hydrogen? It's abundant, clean, efficient, and can be derived from diverse domestic resources. . Distributed Generation Transportation Biomass Hydro Wind Solar Geothermal Coal Nuclear Natural Gas Oil With Carbon Sequestration HIGH EFFICIENCY & RELIABILITY ZERO/NEAR ZERO EMISSIONS 3 President Bush Launches the Hydrogen Fuel Initiative "Tonight I am proposing $1.2 billion in research funding .... "With a new national commitment, our scientists and engineers will overcome obstacles to taking these cars from laboratory to showroom so that the first car driven by a child born today could be powered by hydrogen, and pollution-free. President George W. Bush 2003 State of the Union Address January 28, 2003

375

Corrosion of Membrane Materials for Hydrogen Separation from ...  

Science Conference Proceedings (OSTI)

Abstract Scope, To produce high purity hydrogen fuel from coal, hydrogen can be extracted from syngas using gas separation membranes. No membrane...

376

Hydrogen and Fuel Cell Activities, Progress, and Plans: Report...  

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

2009 Page 1 Hydrogen and Fuel Cell Activities, Progress, and Plans: Report to Congress o Developing technologies for the production of hydrogen from coal that will enable...

377

Development of Inorganic Membranes for Hydrogen Separation  

DOE Green Energy (OSTI)

The purpose of this work is to improve the method of fabricating tubular metal supported microporous inorganic membranes. Earlier work focused on the original development of inorganic membranes for the purification of hydrogen. These membranes are now being scaled up for demonstration in a coal gasification plant for the separation of hydrogen from coal-derived synthesis gas for a project funded by the Office of Fossil Energy's Gasification and Coal Fuels programs [1]. This project is part of FutureGen, an initiative to build the world's first integrated sequestration and hydrogen production research power plant. Although previous work in the Advanced Research Materials Program project led to development of a tubular metal supported microporous membrane which was approved by the Department of Energy for testing, the membranes generally have lower than desired selectivities for hydrogen over other gases common in synthesis gas including carbon dioxide. The work on this project over three years will lead to general improvements in fabrication techniques that will result in membranes having higher separation factors and higher fluxes. Scanning electron microscopy and profilometry data will be presented to show qualitatively and quantitatively the surface roughness of the support tubes. We will discuss how the roughness affects membrane quality and methods to improve the quality of the support tube surface.

Bischoff, Brian L [ORNL; Adcock, Kenneth Dale [ORNL; Powell, Lawrence E [ORNL; Sutton, Theodore G [ORNL; Miller, Curtis Jack [ORNL

2007-01-01T23:59:59.000Z

378

Chemistry and structure of coal-derived asphaltenes, Phase II. Quarterly progress report, January--March 1977. [15 refs  

SciTech Connect

Separations of Synthoil liquefied coal by solvent fractionation and high pressure liquid chromatography have been compared. Solvent fractionation is believed to give more distinctive fractions. The asphaltene fraction obtained by use of hplc was found to be a mixture of resin, asphaltene, carbene, and carboid. Solvent elution chromatrogrphy of asphaltenes on silica gel has been scaled up, and recoveries of 98-99 wt. % are generally obtained. VPO molecular weight studies of coal asphaltenes, as a function of concentration, in the solvents benzene and THF indicate that association of asphaltenes takes place in both solvents, but is more significant in benzene. Structural parameters obtained from modified Brown-Ladner treatment of proton NMR data suggest that solvent fractions: oil, resin, asphaltene, and carboid have structural characteristics which are sequentially related. X-ray diffraction patterns for asphaltene, carbene, and carboid fractions reveal progressively sharpened (002) and (11) bands indicative of increasing carbonization in this series. Methyl iodide addition to a basic fraction of Synthoil asphaltene (diethyl ether-eluted from silica gel) suggests, in conjunction with infrared results, that essentially all of the nitrogen in this fraction is present in basic pyridine-like compounds.

Yen, T. F.

1977-01-01T23:59:59.000Z

379

Co-firing high sulfur coal with refuse derived fuels. Progress report No. 3, [April--June 1995  

DOE Green Energy (OSTI)

The Thermogravimetric Analyzer-Fourier Transform Infrared Spectrometer-Mass Spectrometer (TG-FTIR-MS) system was used to identify molecular chlorine, along with HCl, CO, CO{sub 2}, H{sub 2}O, and various hydrocarbons in the gaseous products of the combustion of PVC resin in air. This is a significant finding that will lead us to examine this combustion step further to look for the formation of chlorinated organic compounds. The combination of TG-FTIR and TG-MS offers complementary techniques for the detection and identification of combustion products from coals PVC, cellulose, shredded newspaper, and various blends of these materials. The pilot atmospheric fluidized bed combustor (AFBC) at Western Kentucky University has been tested. The main purpose of these preliminary AFBC runs were to determine the compatibility of coal and pelletized wood in blends and to explore the effects of flue/air ratio. Our objective is to conduct AFBC burns with 90 percent sulfur capture and more then 96% combustion efficiency.

Pan, Wei-Ping; Riley, J.T.; Lloyd, W.G.

1995-05-31T23:59:59.000Z

380

The economical production of alcohol fuels from coal-derived synthsis gas. Quarterly technical progress report number 10, 1 January 1994--31 March 1994  

DOE Green Energy (OSTI)

The WVU plug-flow microreactor system is now complete. Screening runs with this system will commence. Computer control is being installed in the second WVU unit. Additional hardware has been suggested for this system so that it can be used either to screen additional catalysts or to obtain kinetic data on selected catalyst samples. Synthetic preparations and characterizations of molybdenum-based sulfide and nitride catalysts are ongoing. Modelling studies are continuing satisfactorily. A more detailed model of the reaction kinetics, to account for individual alcohols rather than a lumped highter-alcohol, has been inserted into the model of a plug-flow reactor. A solution methodology to maximize the profitability of alcohol production, separation and blending has been developed. The temperatures, pressures, flowrates, and key component recoveries in the separation steps are the optimization variables. The probability of this process becoming economically feasible in the near future appears to be extremely small given the low return on capital investment associated with the production of alcohol from coal. If coal derived alcohols are to become alternative transportation fuels, then the capital cost associated with the process must be reduced, specifically the cost of the gasifiers, or significant changes need to be made in the composition of the mixed alcohol product. A methodology for performing Monte Carlo studies to determine quantitatively the uncertainties relevant to future decisions to build an alcohol-fuels plant is still being developed.

Not Available

1994-04-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrogen coal derived" 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

Co-firing a pressurized fluidized-bed combustion system with coal and refuse derived fuels and/or sludges. Task 16  

Science Conference Proceedings (OSTI)

The co-firing of waste materials with coal in utility scale power plants has emerged as an effective approach to produce energy and manage municipal waste. Leading this approach, the atmospheric fluidized-bed combustor (AFBC) has demonstrated its commercial acceptance in the utility market as a reliable source of power burning a variety of waste and alternative fuels. The fluidized bed, with its stability of combustion, reduces the amount of thermochemical transients and provides for easier process control. The application of pressurized fluidized-bed combustor (PFBC) technology, although relatively new, can provide significant enhancements to the efficient production of electricity while maintaining the waste management benefits of AFBC. A study was undertaken to investigate the technical and economic feasibility of co-firing a PFBC with coal and municipal and industrial wastes. Focus was placed on the production of electricity and the efficient disposal of wastes for application in central power station and distributed locations. Wastes considered for co-firing include municipal solid waste (MSW), tire-derived fuel (TDF), sewage sludge, and industrial de-inking sludge. Issues concerning waste material preparation and feed, PFBC operation, plant emissions, and regulations are addressed. This paper describes the results of this investigation, presents conclusions on the key issues, and provides recommendations for further evaluation.

DeLallo, M.; Zaharchuk, R.

1994-01-01T23:59:59.000Z

382

Coal liquefaction  

DOE Patents (OSTI)

In a two-stage liquefaction wherein coal, hydrogen and liquefaction solvent are contacted in a first thermal liquefaction zone, followed by recovery of an essentially ash free liquid and a pumpable stream of insoluble material, which includes 850.degree. F.+ liquid, with the essentially ash free liquid then being further upgraded in a second liquefaction zone, the liquefaction solvent for the first stage includes the pumpable stream of insoluble material from the first liquefaction stage, and 850.degree. F.+ liquid from the second liquefaction stage.

Schindler, Harvey D. (Fairlawn, NJ)

1985-01-01T23:59:59.000Z

383

Process for stabilization of coal liquid fractions  

SciTech Connect

Coal liquid fractions to be used as fuels are stabilized against gum formation and viscosity increases during storage, permitting the fuel to be burned as is, without further expensive treatments to remove gums or gum-forming materials. Stabilization is accomplished by addition of cyclohexanol or other simple inexpensive secondary and tertiary alcohols, secondary and tertiary amines, and ketones to such coal liquids at levels of 5-25% by weight with respect to the coal liquid being treated. Cyclohexanol is a particularly effective and cost-efficient stabilizer. Other stabilizers are isopropanol, diphenylmethanol, tertiary butanol, dipropylamine, triethylamine, diphenylamine, ethylmethylketone, cyclohexanone, methylphenylketone, and benzophenone. Experimental data indicate that stabilization is achieved by breaking hydrogen bonds between phenols in the coal liquid, thereby preventing or retarding oxidative coupling. In addition, it has been found that coal liquid fractions stabilized according to the invention can be mixed with petroleum-derived liquid fuels to produce mixtures in which gum deposition is prevented or reduced relative to similar mixtures not containing stabilizer.

Davies, Geoffrey (Boston, MA); El-Toukhy, Ahmed (Alexandria, EG)

1987-01-01T23:59:59.000Z

384

CO-PRODUCTION OF HYDROGEN AND ELECTRICITY USING PRESSURIZED CIRCULATING FLUIDIZED BED GASIFICATION TECHNOLOGY  

DOE Green Energy (OSTI)

Foster Wheeler has completed work under a U.S. Department of Energy cooperative agreement to develop a gasification equipment module that can serve as a building block for a variety of advanced, coal-fueled plants. When linked with other equipment blocks also under development, studies have shown that Foster Wheeler's gasification module can enable an electric generating plant to operate with an efficiency exceeding 60 percent (coal higher heating value basis) while producing near zero emissions of traditional stack gas pollutants. The heart of the equipment module is a pressurized circulating fluidized bed (PCFB) that is used to gasify the coal; it can operate with either air or oxygen and produces a coal-derived syngas without the formation of corrosive slag or sticky ash that can reduce plant availabilities. Rather than fuel a gas turbine for combined cycle power generation, the syngas can alternatively be processed to produce clean fuels and or chemicals. As a result, the study described herein was conducted to determine the performance and economics of using the syngas to produce hydrogen for sale to a nearby refinery in a hydrogen-electricity co-production plant setting. The plant is fueled with Pittsburgh No. 8 coal, produces 99.95 percent pure hydrogen at a rate of 260 tons per day and generates 255 MWe of power for sale. Based on an electricity sell price of $45/MWhr, the hydrogen has a 10-year levelized production cost of $6.75 per million Btu; this price is competitive with hydrogen produced by steam methane reforming at a natural gas price of $4/MMBtu. Hence, coal-fueled, PCFB gasifier-based plants appear to be a viable means for either high efficiency power generation or co-production of hydrogen and electricity. This report describes the PCFB gasifier-based plant, presents its performance and economics, and compares it to other coal-based and natural gas based hydrogen production technologies.

Zhen Fan

2006-05-30T23:59:59.000Z

385

Palladium-hydrogen Interaction in Dislocations: Trapping and ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2010 TMS Annual Meeting & Exhibition. Symposium , Materials in Clean Power Systems V: Clean Coal-, Hydrogen...

386

X. Hydrogen Program Contacts  

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

C. Lowell Miller, Director Office of Sequestration, Hydrogen and Clean Coal Fuels DOE Office of Fossil Energy Phone: 301-903-9453 Email: Lowell.Miller@hq.doe.gov...

387

Small Scale Coal Biomass Liquids Production Using Highly Selective Fischer  

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

Small Scale Coal Biomass Liquids Production Using Highly Selective Fischer Tropsch Catalyst Small Scale Coal Biomass Liquids Production Using Highly Selective Fischer Tropsch Catalyst Southern Research Institute Project Number: FE0010231 Project Description Fischer-Tropsch (FT) process converts a mixture of carbon monoxide and hydrogen, called syngas, into liquid hydrocarbons. It is a leading technology for converting syngas derived from gasification of coal and coal-biomass mixtures to hydrocarbons in coal to liquids (CTL) and coal-biomass to liquids (CBTL) processes. However, conventional FTS catalysts produce undesirable waxes (C21+) that need to be upgraded to liquids (C5-C20) by hydrotreating. This adds significantly to the cost of FTS. The objectives of this project are (i) to demonstrate potential for CBTL cost reduction by maximizing the production of C5-C20 hydrocarbon liquids using a selective FTS catalyst and (ii) to evaluate the impacts of the addition of biomass to coal on product characteristics, carbon foot print, and economics.

388

Coal liquefaction process streams characterization and evaluation  

DOE Green Energy (OSTI)

This study clearly demonstrated the usefulness of liquid- and solid-state {sup 13}C- and {sup 1}H-NMR for the examination of process-derived materials from direct coal liquefaction. The techniques can provide data not directly obtainable by other methods to examine the saturation of aromatic rings and to determine the modes of hydrogen utilization during coal liquefaction. In addition, these methods can be used to infer the extent of condensation and retrograde reactions occurring in the direct coal liquefaction process. Five NMR techniques were employed. Solid-state {sup 13}C-NMR measurements were made using the Cross Polarization Magic Angle Spinning (CP/MAS) and Single Pulse (SP) techniques. Solid-state {sup 1}H-NMR measurements were made using the technique of Combined Rotation and Multiple-Pulse spectroscopy (CRAMPS). Conventional liquid-state {sup 12}C- and {sup 1}H-NMR techniques were employed as appropriate. Interpretation of the NMR data, once obtained, is relatively straightforward. Combined with other information, such as elemental analyses and process conversion data, the NMR data prove to be a powerful tool for the examination of direct coal liquefaction process-derived material. Further development and more wide-spread application of this analytical method as a process development tool is justified on the basis of these results.

Miknis, F.P. (Western Research Inst., Laramie, WY (United States))

1991-11-01T23:59:59.000Z

389

Effects of coal-derived trace species on the performance of molten carbonate fuel cells. Topical report on thermochemical studies  

DOE Green Energy (OSTI)

The overall objective of the present study was to determine in detail the interaction effects of 10 simultaneously present, coal-gas contaminants, both on each other and on components of the Carbonate Fuel Cell. The primary goal was to assess underlying chemistries and reaction mechanisms which may cause decay in fuel cell performance or endurance as a result of both physics-chemical and/or mechanical interactions with the cell components and internal fuel cell parts. It was found, both from theory and cell test evidence, that trace contaminant interactions may occur with: Fuel-cell Electrodes (e.g., in this study with the Ni-anode), Lithium/Potassium Carbonate Electrolyte, Nickel and SS-Hardware, and by Mechanical Obstruction of Gas Flow in the Anode Plenum.

Pigeaud, A.

1991-10-01T23:59:59.000Z

390

Fabrication of Pd/Pd-Alloy Films by Surfactant Induced Electroless Plating for Hydrogen Separation from Advanced Coal Gasification Processes  

SciTech Connect

Dense Pd, Pd-Cu and Pd-Ag composite membranes on microporous stainless steel substrate (MPSS) were fabricated by a novel electroless plating (EP) process. In the conventional Pd-EP process, the oxidation-reduction reactions between Pd-complex and hydrazine result in an evolution of NH{sub 3} and N{sub 2} gas bubbles. When adhered to the substrate surface and in the pores, these gas bubbles hinder uniform Pd-film deposition which results in dendrite growth leading to poor film formation. This problem was addressed by introducing cationic surfactant in the electroless plating process known as surfactant induced electroless plating (SIEP). The unique features of this innovation provide control of Pd-deposition rate, and Pd-grain size distribution. The surfactant molecules play an important role in the EP process by tailoring grain size and the process of agglomeration by removing tiny gas bubbles through adsorption at the gas-liquid interface. As a result surfactant can tailor a nanocrystalline Pd, Cu and Ag deposition in the film resulting in reduced membrane film thickness. Also, it produces a uniform, agglomerated film structure. The Pd-Cu and Pd-Ag membranes on MPSS support were fabricated by sequential deposition using SIEP method. The pre- and post-annealing characterizations of these membranes (Pd, Pd-Cu and Pd-Ag on MPSS substrate) were carried out by SEM, EDX, XRD, and AFM studies. The SEM images show significant improvement of the membrane surface morphology, in terms of metal grain structures and grain agglomeration compared to the membranes fabricated by conventional EP process. The SEM images and helium gas-tightness studies indicate that dense and thinner films of Pd, Pd-Cu and Pd-Ag membranes can be produced with shorter deposition time using surfactant. H{sub 2} Flux through the membranes fabricated by SIEP shows large improvement compared to those by CEP with comparable permselectivity. Pd-MPSS composite membrane was subjected to test for long term performance and thermal cycling (573 - 723 - 573 K) at 15 psi pressure drop for 1200 hours. Pd membranes showed excellent hydrogen permeability and thermal stability during the operational period. Under thermal cycling (573 K - 873 K - 573 K), Pd-Cu-MPSS membrane was stable and retained hydrogen permeation characteristics for over three months of operation. From this limited study, we conclude that SIEP is viable method for fabrication of defect-free, robust Pd-alloy membranes for high-temperature H{sub 2}-separation applications.

Ilias, Shamsuddin; Kumar, Dhananjay

2012-07-31T23:59:59.000Z

391

International Pittsburgh Coal Conference, Sept 15-19, 2003, Pittsburgh...  

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

15-19, 2003, Pittsburgh, PA, USA Paper No. 40-3 (Hydrogen from Coal) Overview of Hydrogen Production Options for Hydrogen Energy Development, Fuel-Cell Fuel Processing and...

392

Pretreatment of coal during transport  

SciTech Connect

Many available coals are "caking coals" which possess the undesirable characteristic of fusing into a solid mass when heated through their plastic temperature range (about 400.degree. C.) which temperature range is involved in many common treatment processes such as gasification, hydrogenation, carbonization and the like. Unless the caking properties are first destroyed, the coal cannot be satisfactorily used in such processes. A process is disclosed herein for decaking finely divided coal during its transport to the treating zone by propelling the coal entrained in an oyxgen-containing gas through a heated transport pipe whereby the separate transport and decaking steps of the prior art are combined into a single step.

Johnson, Glenn E. (Pittsburgh, PA); Neilson, Harry B. (Clairton, PA); Forney, Albert J. (Coraopolis, PA); Haynes, William P. (Pittsburgh, PA)

1977-04-19T23:59:59.000Z

393

EFFECTS OF LEWIS ACID CATALYSTS ON THE HYDROGENATION AND CRACKING OF TWO-RING AROMATIC AND HYDROAROMATIC STRUCTURES RELATED TO COAL  

E-Print Network (OSTI)

Using Zinc Chloride Catalysts in an Extracting Medium", LBL-EFFECTS OF LEWIS ACID CATALYSTS ON THE HYDROGENATION ANDEffects of Lewis Acid Catalysts on the Hydrogenation and

Salim, Sadie S.

2013-01-01T23:59:59.000Z

394

Low-rank coal research  

DOE Green Energy (OSTI)

This work is a compilation of reports on ongoing research at the University of North Dakota. Topics include: Control Technology and Coal Preparation Research (SO{sub x}/NO{sub x} control, waste management), Advanced Research and Technology Development (turbine combustion phenomena, combustion inorganic transformation, coal/char reactivity, liquefaction reactivity of low-rank coals, gasification ash and slag characterization, fine particulate emissions), Combustion Research (fluidized bed combustion, beneficiation of low-rank coals, combustion characterization of low-rank coal fuels, diesel utilization of low-rank coals), Liquefaction Research (low-rank coal direct liquefaction), and Gasification Research (hydrogen production from low-rank coals, advanced wastewater treatment, mild gasification, color and residual COD removal from Synfuel wastewaters, Great Plains Gasification Plant, gasifier optimization).

Not Available

1989-01-01T23:59:59.000Z

395

Coal Liquefaction desulfurization process  

DOE Patents (OSTI)

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

Givens, Edwin N. (Bethlehem, PA)

1983-01-01T23:59:59.000Z

396

NETL: News Release - Enabling Turbine Technologies for Hydrogen Fuels  

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

September 8, 2005 September 8, 2005 Enabling Turbine Technologies for Hydrogen Fuels Turbine Program Advances Ultra-Clean, Coal-Based Systems WASHINGTON, DC - The Department of Energy's Office of Fossil Energy Turbine Technology R&D Program was recently expanded with the selection of 10 new projects valued at $130 million. The new program will advance turbines and turbine subsystems for integrated gasification combined cycle (IGCC) power plants, and address the use of hydrogen in small-scale turbines for industrial applications. Resulting technologies will operate cleanly and efficiently when fueled with coal-derived hydrogen or synthesis gas. Turbines can generate electrical power on a large scale-in central power stations sized 250 megawatts and larger-or on a small scale-in local, industrial power systems sized 1-100 megawatts. Small-scale systems also produce mechanical power for jet engines, compressors, heating systems, and other applications.

397

Two stage liquefaction of coal  

SciTech Connect

A two stage coal liquefaction process and apparatus comprising hydrogen donor solvent extracting, solvent deashing, and catalytic hydrocracking. Preferrably, the catalytic hydrocracking is performed in an ebullating bed hydrocracker.

Neuworth, Martin B. (Chevy Chase, MD)

1981-01-01T23:59:59.000Z

398

DOE Hydrogen and Fuel Cells Program: 2007 Annual Progress Report  

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

7 7 Printable Version 2007 Annual Progress Report The 2007 Progress Report for the DOE Hydrogen Program summarizes the hydrogen and fuel cell R&D activities and accomplishments for FY 2007. Published in November 2007, the full document is very large; each technical report is available as an individual Adobe Acrobat PDF. Download Adobe Reader. Front Cover (PDF 711 KB) Table of Contents (PDF 236 KB) I. Introduction, JoAnn Milliken, U.S. Department of Energy (PDF 821 KB) II. Hydrogen Production Distributed Production from Natural Gas Distributed Production from Bio-Derived Liquids Electrolysis Separations Central Biomass Gasification Solar Hi-Temp Thermochemical Water Splitting Photoelectrochemical Biological Production Hydrogen from Coal Nuclear Hydrogen Initiative

399

Development of coker feeds from aromatic oil and bituminous coal digests.  

E-Print Network (OSTI)

??Kingwood coal has been digested with two coal derived (anthracene oil and carbon black base) and two petroleum derived (slurry oil and Maraflex oil) aromatic (more)

Clendenin, L. Mitchell.

2004-01-01T23:59:59.000Z

400

HYDROGENATION AND CRACKING OF COAL RELATED FUSED-RING STRUCTURES USING ZnCl2 AND AlCl3 CATALYSTS  

E-Print Network (OSTI)

effective catalyst for coal gasification at severe reactionliquefaction as well as gasification has been observed (3).and susceptibility to gasification (4,5). of Ross et al.

Salim, Sadie S.

2013-01-01T23:59:59.000Z

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


401

DOE Hydrogen Analysis Repository: H2A Case Study: Current Central...  

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

Coal without Sequestration Project Summary Full Title: H2A Case Study: Current (2005) Hydrogen from Coal without CO2 Capture and Sequestration Project ID: 231 Principal...

402

Coal liquefaction process using pretreatment with a binary solvent mixture  

DOE Patents (OSTI)

An improved process for thermal solvent refining or hydroliquefaction of non-anthracitic coal at elevated temperatures under hydrogen pressure in a hydrogen donor solvent comprises pretreating the coal with a binary mixture of an aromatic hydrocarbon and an aliphatic alcohol at a temperature below 300.degree. C. before the hydroliquefaction step. This treatment generally increases both conversion of coal and yields of oil.

Miller, Robert N. (Allentown, PA)

1986-01-01T23:59:59.000Z

403

Coal plasticity at high heating rates and temperatures  

SciTech Connect

Effects of coal type on coal plasticity are investigated. Seven coals, from the Argonne premium sample bank ranging from lignite to low volatile bituminous, are studied. Different indices and structural data of a coal are shown to affect its plastic behavior. A coal-specific parameter incorporating the effects of labile bridges, oxygen, and hydrogen on plasticity has been used to successfully correlate measured values of maximum plasticity (i.e. minimum apparent viscosity) at elevated temperature with coal type.

Gerjarusak, S.; Peters, W.A.; Howard, J.B.

1992-01-01T23:59:59.000Z

404

Coal liquefaction process streams characterization and evaluation. Solid-state NMR characterization of coal liquefaction products  

DOE Green Energy (OSTI)

This study clearly demonstrated the usefulness of liquid- and solid-state {sup 13}C- and {sup 1}H-NMR for the examination of process-derived materials from direct coal liquefaction. The techniques can provide data not directly obtainable by other methods to examine the saturation of aromatic rings and to determine the modes of hydrogen utilization during coal liquefaction. In addition, these methods can be used to infer the extent of condensation and retrograde reactions occurring in the direct coal liquefaction process. Five NMR techniques were employed. Solid-state {sup 13}C-NMR measurements were made using the Cross Polarization Magic Angle Spinning (CP/MAS) and Single Pulse (SP) techniques. Solid-state {sup 1}H-NMR measurements were made using the technique of Combined Rotation and Multiple-Pulse spectroscopy (CRAMPS). Conventional liquid-state {sup 12}C- and {sup 1}H-NMR techniques were employed as appropriate. Interpretation of the NMR data, once obtained, is relatively straightforward. Combined with other information, such as elemental analyses and process conversion data, the NMR data prove to be a powerful tool for the examination of direct coal liquefaction process-derived material. Further development and more wide-spread application of this analytical method as a process development tool is justified on the basis of these results.

Miknis, F.P. [Western Research Inst., Laramie, WY (United States)

1991-11-01T23:59:59.000Z

405

NETL: Coal and Coal/Biomass to Liquids  

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

C&CBTL C&CBTL Coal and Power Systems Coal and Coal/Biomass to Liquids The Coal and Coal/Biomass to Liquids program effort is focused on technologies to foster the commercial adoption of coal and coal/biomass gasification and the production of affordable liquid fuels and hydrogen with excellent environmental performance. U.S. Economic Competitiveness U.S. Economic Competitiveness U.S. Economic Competitiveness U.S. Economic Competitiveness Advanced Fuels Synthesis U.S. Economic Competitiveness U.S. Economic Competitiveness U.S. Economic Competitiveness U.S. Economic Competitiveness Advanced Fuels Synthesis Systems Analyses Global Environmental Benefits Global Environmental Benefits Global Environmental Benefits Global Environmental Benefits Global Environmental Benefits Global Environmental Benefits

406

The economical production of alcohol fuels from coal-derived synthesis gas. Quarterly report, October 1, 1996--December 31, 1996  

DOE Green Energy (OSTI)

The objective of Task 1 is to prepare and evaluate catalysts and to develop efficient reactor systems for the selective conversion of hydrogen-lean synthesis gas to alcohol fuel extender and octane enhancers. Task 1 is subdivided into three separate subtasks: laboratory and equipment setup; catalysis research; and reaction engineering and modeling. Research at West Virginia University (WVU) is focused on molybdenum-based catalysts for higher alcohol synthesis. Parallel research carried out at Union Carbide Corporation (UCC) is focused on transition-metal-oxide catalysts. During this time period, at WVU, we tried several methods to eliminate problems related to condensation of heavier products when reduced Mo-Ni-K/C materials were used as catalysts. We then resumed our kinetic study on the reduced Mo-Ni-K/C materials were used as catalysts. We then resumed our kinetic study on the reduced Mo-Ni-K/C catalysts. We have also obtained same preliminary results in our attempts to analyze quantitatively the temperature-programmed reduction spectra for C- supported Mo-based catalysts. We have completed the kinetic study for the sulfided Co-K-MoS{sub 2}/C catalyst. We have compared the results of methanol synthesis using the membrane reactor with those using a simple plug-flow reactor. At UCC, the complete characterization of selected catalysts has been completed. The results suggest that catalyst pretreatment under different reducing conditions yield different surface compositions and thus different catalytic reactivities.

NONE

1997-01-01T23:59:59.000Z

407

Separating lignite hydrogenation sludge by vacuum distillation  

SciTech Connect

Vacuum distillation was studied as a means to separate coal hydrogenation sludge. Additives containing mainly aromatic hydrocarbons intensified the process. 4 refs., 2 figs., 5 tabs.

Gorlov, E.G.; Grobanova, L.T.; Belyavtseva, N.V. [Rossiskaya Akademiya, Nauk (Russian Federation)

1994-12-31T23:59:59.000Z

408

Survey of the Economics of Hydrogen Technologies  

E-Print Network (OSTI)

Hydrogen Production Steam Methane Reforming Noncatalytic Partial Oxidation Coal Gasification Biomass Combustion Engines Hybrid Vehicles Onboard Storage Onboard Reforming Refueling Options Where possible

409

Materials for Hydrogen Production, Storage, and Distribution  

Science Conference Proceedings (OSTI)

Feb 16, 2010 ... Co-Production of Pure Hydrogen and Electricity from Coal Syngas via the .... and plastic deformations in the crack tip energy rate formulate.

410

NETL: Gasification Systems - Advanced Hydrogen Transport Membranes...  

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

Advanced Hydrogen Transport Membranes for Coal Gasification Project No.: DE-FE0004908 Membranes shown (from top to bottom): ceramic support, activated and coated with palladium...

411

NETL: Gasification - Advanced Hydrogen Transport Membranes for...  

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

Syngas Processing Systems Advanced Hydrogen Transport Membranes for Coal Gasification Praxair Inc. Project Number: FE0004908 Project Description Praxair is conducting research to...

412

Materials Metrology for a Hydrogen Distribution Infrastructure  

Science Conference Proceedings (OSTI)

Addressing Materials Processing Issues for USC Steam Turbines: Cast Versions of ... Co-Production of Pure Hydrogen and Electricity from Coal Syngas via the...

413

Scale-Up of Hydrogen Transport Membranes  

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

feedstocks, such as coal, are converted into gaseous components, called synthesis gas (syngas), a mixture of hydrogen (H 2 ) and carbon monoxide (CO). The syngas can be further...

414

Integration of carbonate fuel cells with advanced coal gasification systems  

DOE Green Energy (OSTI)

Carbonate fuel cells have attributes which make them ideally suited to operate on coal-derived fuel gas; they can convert the methane, hydrogen, and carbon monoxide present in coal derived fuel gas directly to electricity, are not subject to thermodynamic cycle limits as are heat engines, and operate at temperatures compatible with coal gasifiers. Some new opportunities for improved efficiency have been identified in integrated coal gasification/carbonate fuel cells which take advantage of low temperature catalytic coal gasification producing a methane-rich fuel gas, and the internal methane reforming capabilities of Energy Research Corporation's carbonate fuel cells. By selecting the appropriate operating conditions and catalyst in the gasifier, methane formation is maximized to improve gasification efficiency and to take advantage of the heat management aspects of the internal reforming carbonate fuel cell. These advanced integrated gasification/carbonate fuel cell systems are projected to have better efficiencies than gasification/carbonate fuel cell systems employing conventional gasification, and also competing non-fuel cell systems. These improved efficiencies would be accompanied by a corresponding reduction in impact on the environment as well.

Steinfeld, G. (Energy Research Corp., Danbury, CT (United States)); Meyers, S.J. (Fluor Daniel, Inc., Irvine, CA (United States)); Hauserman, W.B. (North Dakota Univ., Grand Forks, ND (United States). Energy and Environmental Research Center)

1992-01-01T23:59:59.000Z

415

Integration of carbonate fuel cells with advanced coal gasification systems  

DOE Green Energy (OSTI)

Carbonate fuel cells have attributes which make them ideally suited to operate on coal-derived fuel gas; they can convert the methane, hydrogen, and carbon monoxide present in coal derived fuel gas directly to electricity, are not subject to thermodynamic cycle limits as are heat engines, and operate at temperatures compatible with coal gasifiers. Some new opportunities for improved efficiency have been identified in integrated coal gasification/carbonate fuel cells which take advantage of low temperature catalytic coal gasification producing a methane-rich fuel gas, and the internal methane reforming capabilities of Energy Research Corporation`s carbonate fuel cells. By selecting the appropriate operating conditions and catalyst in the gasifier, methane formation is maximized to improve gasification efficiency and to take advantage of the heat management aspects of the internal reforming carbonate fuel cell. These advanced integrated gasification/carbonate fuel cell systems are projected to have better efficiencies than gasification/carbonate fuel cell systems employing conventional gasification, and also competing non-fuel cell systems. These improved efficiencies would be accompanied by a corresponding reduction in impact on the environment as well.

Steinfeld, G. [Energy Research Corp., Danbury, CT (United States); Meyers, S.J. [Fluor Daniel, Inc., Irvine, CA (United States); Hauserman, W.B. [North Dakota Univ., Grand Forks, ND (United States). Energy and Environmental Research Center

1992-12-01T23:59:59.000Z

416

Synthesis of acrylates and methacrlyates from coal-derived syngas. Quarterly technical progress report, January 1, 1995--March 31, 1995  

DOE Green Energy (OSTI)

The objective Task 1, Synthesis of Propionates, is to develop the technology for the synthesis of low-cost propionates. These propionates are the basic feedstock for the subsequent reaction with formaldehyde to produce the target molecule, methyl methacrylate (MMA). Eastman has explored several possible routes to the propionates and has concluded that the most promising is the synthesis of propionic anhydride from the reaction of propionic acid from and ethylene (and also hydrogen in some cases). The main advantage of the anhydride over the acid is that its subsequent reaction with formaldehyde does not produce water, which can lead to undesired byproducts. Bechtel is carrying out a cost analysis of the Eastman route to the anhydride to determine if it is potentially competitive with commercially practiced routes to the same molecule. The answer is expected next quarter. The objective Task 2, Condensation Catalysis to develop catalysts for the condensation of the propionate (propionic anhydride is our target molecule) with formaldehyde. This reaction produces methacrylic acid (MAA), which would then be reacted with methanol to produce MMA in the slurry reactor. We have synthesized a wide range of catalysts and the results show that there is substantial byproduct formation, including 3-pentanone and some propionic acid. Our results show the highest yields of MAA using an alkalized alumina (1%Na/{sub y}-AI{sub 2}O{sub 3}). Although the condensation of propionic acid with formaldehyde is well studied in the literature, little is reported on the condensation of the anhydride. Although it is likely that the same general types of acid/base catalysts that promote the acid condensation will also promote that of the anhydride, the strength and balance of the acid and base sites is likely to be different. We plan to explore the relationship of the catalyst properties and MMA yields using the Altamira system, due to be delivered this next quarter.

Tischer, R.E.; Spivey, J.J.

1995-08-01T23:59:59.000Z

417

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

418

Materials for Hydrogen Production, Separation, and Storage  

Science Conference Proceedings (OSTI)

Mar 13, 2012 ... Materials in Clean Power Systems VII: Clean Coal-, Hydrogen ... and Fuel Cells: Materials for Hydrogen Production, Separation, and Storage .... Mixed Conducting Molten Salt Electrolyte for Na/NiCl2 Cell: Tannaz Javadi1;...

419

Development of alcohol-based synthetic transportation fuels from coal-derived synthesis gases. First quarterly progress report, September 14-December 31, 1979  

DOE Green Energy (OSTI)

Chem Systems is carrying out an experimental program for the conversion of coal-derived synthesis gases to a mixture of C/sub 1/-C/sub 4/ alcohols. The objec