- Details
Molecular Catalytic Coal Liquid Conversion
United States Department of Energy Grant
#DE-AC22-91PC91056
Leon M. Stock - Principal Investigator
Government. Neither the United States Government nor any agency thereof, nor any of their
employees, makes any warranty, express or implied, or assumes any legal liability or responsibility
for the accuracy, completeness, or usefulness of any information, apparatus, product, or
process disclosed, or represents that its use would not infringe privately owned rights. Reference
herein to any specific commercial product, process, or service by trade name, trademark,
manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation,
or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof.
Quarterly Progress Report
Molecular Catalytic Coal Liquid Conversion
#DE-AC22-91 PC91056
Michael Ettinger
Research Staff
Molecular Catalytic Coal Liquid Conversion
Last quarter, substantial progress has been made in the two general tasks advanced in our research proposal. The first task consists of the development of molecular homogeneous catalysts that can be used in the hydrogenation of coal liquids and in coal conversion processes. The second task concerns the activation of dihydrogen by basic catalysts in homogeneous reaction systems. With regards to the first task, we have prepared two organometallic rhodium (I) catalysts.
aromatic hydrocarbons and aromatic compounds containing the ether group, alkyl groups, amino and carbonyl groups. However, both compounds were totally ineffective in catalyzing the hydrogenation of sulfur-containing aromatic organic compounds. Nevertheless, both rhodium catalysts successfully catalyzed the hydrogenation of naphthalene even in the presence of the coal liquids. With regards to base-activated hydrogenation of organic compounds, we have found that hydroxide and alkoxide bases are capable of activating dihydrogen, thereby leading to the hydrogenation of phenyl-substituted alkenes. Thus far, we are the first group to apply this unusual method towards the successful hydrogenation of olefins.
(There is an involved dissertation regarding organometallic catalysts, which we don't include here, but which invites reading by qualified coal partisans.)
hydrogen to organic molecules under relatively mild conditions. We shall investigate whether basic catalysts ranging from hydroxide to hydrosulfide ion can accomplish the addition of dihydrogen to coal liquids and the removal of heteroatoms from them.
This phase of the project essentially consists of preparing organometallic reagents which are known or have been reported to act as homogeneous hydrogenation catalysts of aromatic hydrocarbons and studying their properties as homogeneous hydrogenation catalysts under various conditions with the ultimate objective of using these compounds to catalyze the conversion of coal liquids.
II. Base-Catalyzed Hydrogenation
Our second task is to investigate the chemistry of base-catalyzed hydrogenation of organic compounds with the ultimate objective of applying the chemistry behind this novel concept to the catalytic conversion of coal liquids.
- Details
"Hydrogenation of COED Coal Oils
ducting hydrogenation experiments on coal derived oils, was requested by the Office of Coal Research to hydrotreat some COED oils. Accordingly, the following work was carried out by ARC0 in cooperation with FMC.
coking.
"Conclusion
- Details
Coal-to-Liquids Products Industry Overview
Proposed Rule for Mandatory Reporting of Greenhouse Gases
Office of Air and Radiation; U.S. Environmental Protection Agency
January 28, 2009
Coal-to-Liquids Product Suppliers Technical Support Document
1.1. Purpose........................................................................................................1
1.2. Organization of this Report...........................................................................1
2.0. Overview of the Coal-to-Liquids Industry..................................................................1
2.1. Three Technologies......................................................................................2
2.1.1 Fischer-Tropsch (FT)....................................................................................2
2.1.2 Methanol to Gasoline (MTG)........................................................................5
2.1.3 Direct Liquefaction .......................................................................................5
2.1.4 Products.......................................................................................................7
3.0. Plants. .....................................................................................................................8
3.1. Existing Plants..............................................................................................8
3.2. Planned Plants.............................................................................................9
4.0. Carbon Content of Products.....................................................................................9
Exhibit 2: Coal to Liquids Flow Diagram (Fischer Tropsch Synthesis).............................4
Exhibit 3: Coal to Liquids Flow Diagram (Direct Liquefaction) .........................................6
Exhibit 4: Sasol CTL Synthetic Jet Fuel...........................................................................9
This document provides an overview of the status of the emerging coal-to-liquids (CTL)
industry both in the United States and elsewhere. The analysis here is part of a larger
effort to develop guidelines for mandatory reporting requirements for greenhouse gases
(GHGs). In December 2007, Congress enacted an omnibus appropriations bill that
directs EPA to develop and publish a rule requiring measurement and reporting of GHG
emissions above appropriate thresholds in all sectors of the economy. The bill
mandates that EPA publish a proposed rule within nine months and a final rule within 18
months. Understanding the information that fuel suppliers already generate and report
to federal agencies is a first step in developing mandatory GHG reporting requirements.
document focuses more on the status of the industry, the emerging technologies, and
identifies the operational plants and those that are planned.
products from a CLT plant, particularly a plant using Fischer Tropsch technology, have a
different and potentially lower carbon content compared to those from a conventional
petroleum refinery. However, data are difficult to identify and the current approach, until
further knowledge is available, is to use the petroleum default table in Subpart MM
Petroleum Suppliers to calculate the carbon content of CTL derived products.
To provide context for the CTL sector, section 2 provides an overview of the industry and
focuses on the two dominant technologies, the indirect Fischer Tropsch and direct
liquefaction of coal. There is too a brief discussion of Mobil’s methanol-to-gasoline
(MTG) process. There is also some discussion of the type of products that come from a
CLT plant and whether or not they need further processing. Section 3 discusses the
existing plants, plants that are under construction and planned plants. Since this is a
nascent industry the discussion is not confined only to the United States. Finally,
Section 4 focuses on what is known about the carbon content of CTL products.
Coal-to-Liquids technology has been known and used for a long time. The underlying
technology, coal gasification, was developed in the 19th century, the product being “town
gas” which was used for lighting and cooking. Use of town gas became widespread in
both Europe and the United States. In the 1920s the Fischer-Tropsch process was
developed to convert the main constituents of the gas, hydrogen and carbon monoxide
to liquid fuels.
reacting coal with hydrogen and process solvent at high temperatures and pressure to
produce liquid fuels. This direct liquefaction process was used to produce high octane
aviation gasoline by Germany during World War II. The Fischer Tropsch technology
the very low prices of petroleum its only use came towards the end of the Nazi regime in
Germany and during the period of apartheid in South Africa. Sanctions and war cut off
most petroleum to these two countries so that need rather than prices determined the
use of the technology.
plants were planned before the substantial increase in crude oil prices commencing after
2000. The substantial increase in crude oil prices, combined with concern over
geopolitical instability in the major producing areas, and the increasing competition for
limited resources has resulted in attention once again turning to alternative sources for
transportation fuels, whether biofuels, gas to liquids, coal gasification, or coal to liquids.
Oil prices, driven by burgeoning global demand have reached a high enough level that
these alternative sources, despite the unprecedented increase in capital and operating
costs, can be deemed economic as well as technically feasible. CTL is the subject of
increasing attention as coal resources are widespread and voluminous.
end technology of gasification has advanced considerably. Between 2000 and 2007, 27
new coal gasification facilities became operational around the world. Three of these
plants produce electrical power using a combination of steam and gas, and the others
are used to produce synthesis gas for the manufacture of chemicals, particularly
ammonia and methanol. Consequently, there have been significant advances in coal
gasification.
There are currently three established technologies for CTL plants: the indirect
method in which coal is first gasified and then converted to liquid fuels through
the process of Fischer Tropsch synthesis; the MTG process, which is a subset of
the indirect method; and the direct method in which coal is directly converted to
liquid fuels with the help of hydrogen and heavy oils. Exhibit 1 lists all the current
component technologies for CTL.
Exhibit 2 presents a flow diagram of the Sasol CTL process. Sasol has
developed two technologies based on the Fischer Tropsch process: 1) the High
Temperature Fischer Tropsch process which can be used to produce a slate of
light products as well as the building blocks of high value added chemicals, and
2) the Low Temperature Fischer Tropsch process that is used for producing
diesel from coal.
fed to gasifiers to produce raw gas which is then purified into the synthesis gas (a
mixture of hydrogen and carbon monoxide) which is then fed into the Fischer
catalyst.
from a variety of feedstocks other than coal. Commercial development over the
past 20 years has centered around using various deposits of stranded gas. The
resulting various Gas-to-Liquids plants all use a variation of the FT process.
Considerable work has also been done examing adding biomass to the coal
feedstock as a means of reducing stationary source greenhouse gas emissions.
through a conventional petroleum refinery depending on the product slate
required.
2.Two-Stage Direct Liquefaction
3. Co-Processing and Dry Hydrogenation
4. Indirect Liquefaction
5. Liquids from Coal (LFC) Process
6. Encoal Coal Technology Corporation
7. Univ. of North Dakota Energy and Environmental Center (EERC)/AMAX R&D Process
8. Institute of Gas Technology
9. Char Oil Energy Development (COED) - (FMC, ARCO - JtM)
10. Solvent Refined Coal Processes (SRC-I and SRC-II) Gulf Oil
11. Exxon Donor Solvent (EDS) Process
12. H-Coal Process – HRI
13. Imhausen High-Pressure Process
14. Conoco Zinc Chloride Process
15. Kohleoel Process – Ruhrkohle
16. NEDO Process (Japan - JtM)
17.Consol Synthetic Fuel (CSF) Process
18. Lummus ITSL Process
19. Chevron Coal Liquefaction Process (CCLP)
20. Kerr-McGee ITSL Work
21. Mitsubishi Solvolysis Process
22. Pyrosol Process – Saarbergwerke -Catalytic
24. Liquid Solvent Extraction (LSE) Process
25. British Coal-Brown Coal Liquefaction (BCL) Process
27. Amoco CC-TSL Process
28. Supercritical Gas Extraction (SGE) Process
29. British Coal -MITI Mark I and Mark II
Co-Processing
30. Cherry P Process – Osaka Gas Co.
31. Solvolysis Co-Processing – Mitsubishi
32. Mobil Co-Processing
33. Pyrosol Co-Processing
34. Saabergwerke
36. Lummus Crest Co-Processing
37. Alberta Research Council Co-Processing
38. CANMET Co-Processing
39. Rheinbraun Co-Processing
40. TUC Co-Processing
41. UOP Slurry-Catalysed Co-Processing
42. HTI Co-Processing
43. Sasol
44. Rentech
45. Syntroleum
47. Mobil Methanol-to-Olefins (MTO) Process
48. Shell Middle Distillate Synthesis (SMOS)
Coal-to-Liquids Product Suppliers Technical Support Document
The front end of a MTG plant encompassing coal gasification would be identical
to that of a CTL plant. However, the coal gasification has to produce a synthesis
gas with a hydrogen-to-carbon monoxide ratio suitable for methanol synthesis.
Once the methanol is produced it is dehydrated to produce dimethyl ether. The
latter is then converted to a mix of hydrocarbons in the presence of special
catalysts. The hydrocarbon mix that results from this is very similar to that found
in raw gasoline. Products from the MTG process are about 90 percent gasoline
with the rest being LPG. Both products can be sold directly into the market.
Commercial methanol is largely produced by natural gas-derived synthesis gas.
There is, however, one commercial plant in the United States where methanol is
produced from coal derived synthesis gas. In these cases the product desired is
methanol, but a commercial scale MTG plant operated in New Zealand from
1985 to 1995 and produced 14,500 barrels per day of gasoline.
process conditions (3500psi/230bar+ and 750F/400C compared to 375psi/25 bar
and 400-630F/200-340C) and expensive feedstocks. In addition, more advances
have been made to the Fischer Tropsch process technology and catalysts than
to direct liquefaction.
Low Temperature process maximizes diesel fuel, while the High Temperature
process maximizes gasoline. Generally speaking the focus has been to produce
transportation fuels and chemical feedstocks, but naphthas and waxes are
always produced irrespective of the process. Considerable work has been done
in South Africa and in the United States on jet fuels for both commercial and
military aircraft.
kerosene to international airlines operating out of Johannesburg Airport. In April
of 2008 international aviation authorities approved Sasol’s fully synthetic CTL jet
fuel as Jet A-1 for commercial use in all turbine aircraft. Currently ASTM is
working to incorporate the synthetic jet fuel in ASTM D1655-08a Standard
Specifications for Aviation Turbine Fuels. A blend of conventional JP8 and FT jet
fuel has recently (2006) been certified for use by the U.S. Air Forces.
fully fungible with petroleum-based jet fuel. Testing on FT jet fuel has revealed
significantly reduced particulate emissions compared to conventional and military
jet fuels.3 Exhibit 4 shows the flow diagram for the manufacturing process in the
High Temperature Fischer Tropsch process.
to produce a new Fischer Tropsch fuel that will meet all of the agency’s needs
and that will be fungible with petroleum based products and thus able to use the
existing infrastructure.
has less than 1 percent aromatics and thus has a high cetane value, generally
from 70 to 80. In general high cetane-number fuels reduce hydrocarbon and
soot emissions from cold starts and reduce nitrogen oxide and particulate
emissions from a warm engine. FT diesel can be sold as a premium product or
can be blended with conventional diesel fuel to improve its qualities. Currently,
there is no approved ASTM test for FT diesel, but apparently ASTM is working on
a test that it is not yet ready to publish.4
would be equal or superior to conventional gasoline and would have positive
effects on air quality relative to benzene and Reid vapour pressure.
propane. This LPG could either be sold directly into the market or to the
petrochemical industry, or could be used at the plant itself to generate electricity.
naphthas and middle distillates. There is considerable variation in the properties
of these products, depending of course on the configuration of the plant, but
unlike the products of either FT plants or MTG plants, these products cannot be
sold directly in to the market place. In general direct liquefaction products
contain more aromatics and cyclic hydrocarbons and they may have an overall
lower hydrogen content. These products would either have to be upgraded at
the plant or sent to a refinery for further upgrading.
Sasol Chemical Industries became operational in the late 1950s. Sasol Two and
Three at Secunda were built in 1974 and 1978. The two plants, now combined
into one, produce approximately 160,000 b/d of mostly transportation products.
Both plants use the Fischer Tropsch indirect CTL technology.
Erdos, Inner Mongolia that will be run by the Shenhua Group, China’s largest
coal miner. This plant, developed in conjunction with the University of West
Virginia, uses direct liquefaction technology. It is expected to convert 3.5 million
tonnes of coal per year into 1 million tonnes of oil products when operational,
predominantly diesel for transportation.
two Fischer Tropsch CTL plants in the provinces of Shaanxi and Ningxia. Two
smaller CTL plants are also under construction in China as is one in Indonesia.
Coal-to-Liquids Product Suppliers Technical Support Document
3.2. Planned Plants
Currently there are fourteen CTL plants under consideration in the United States.
Three are at the design stage with the others still being studied for feasibility.
While most are CTL plants a number of the Rentech proposed plants will be
more complex with feedstock varying from waste to biomass to petroleum coke
as well as coal. Whether any will come to fruition remains to be seen.
There is very little hard data on the carbon content of the products of CTL plants.
The literature does seem to imply that the Fischer Tropsch products will have
lower CO2 emissions when combusted. FT products contain very little aromatics
which would indicate that the carbon content of FT products may be lower than
that of conventional petroleum products. In testimony before the Subcommittee
on Energy and Environment of the U.S. House of Representatives the following
statement was made by a senior scientist from Rentech:
Coal-to-Liquids Product Suppliers Technical Support Document
immediate reduction in particulate emissions. F-T jet fuel has been shown
in laboratory combusters and engines to reduce PM emissions by 96% at
idle and 78% under cruise operation. Validation of the reduction in other
turbine engine emissions is still under way. Concurrent to the PM
reductions is an immediate reduction in CO2 emissions from F-T fuel. F-T
fuels inherently reduce CO2 emissions because they have higher energy
content per carbon content of the fuel, and the fuel is less dense than
conventional jet fuel allowing aircraft to fly further on the same load of fuel.
CTL plant in the United States, EPA is proposing that, until more data becomes
available, reporters from future CTL plants use the default table in Subpart MM –
Suppliers of Petroleum Products of the rule.
especially those products from direct liquefaction plants. Given that petroleum
refineries are required under the rule to keep track of all non-crude feedstocks
that enter the refinery there should not be any double counting. If CTL products
are imported either they will go straight to the market place or to a refinery for
upgrading. In either case there will be little possibility of double counting."
- Details
Project Information | |
Project ID: | DE-FC26-99FT40540 |
Project Title: | Cooperative Research in CI Chemistry |
FE Program: | Adv. Research - Technology Crosscut |
Research Type: | Basic Research |
Funding Memorandum: | Cooperative Agree't (nonCCT) - Tech R&D |
Project Performer | |
Performer Type: | State Higher Education Institution |
Performer: | Consortium for Fossil Fuel Liquefaction Science 201 Kinkead Hall |
Project Team Members: |
|
Project Location | |
City: | Lexington |
State: | Kentucky |
Zip Code: | 40506-0001 |
Congressional District: | 06 |
Responsible FE Site: | NETL |
Project Point of Contact | |
Name: | Huffman, Gerald P. |
Telephone: | (859) 257-4027 |
Fax Number: | (859) 257-7215 |
Email Address: | |
Fossil Energy Point of Contact | |
Name: | Krastman, Don |
Telephone: | (412) 386-4720 |
Location: | NETL |
Email Address: | |
Project Dates | |
Start Date: | 04/28/1999 |
End Date: | 06/30/2003 |
Contract Specialist | |
Name: | Gruber, Thomas J. |
Telephone: | (412) 386-5897 |
Cost & Funding Information | |
Total Est. Cost: | $5,694,068 |
DOE Share: | $4,500,000 |
Non DOE Share: | $1,194,068 |
Project Description | |
A major goal of the CFFLS C1 program is to develop technology for the conversion of methanol into transportation fuels and chemicals. Complementary goals include development of improved technology for the production of syngas from natural gas by reforming with carbon dioxide, new catalysts and processes for the production of hydrogen, technology for producing methanol from syngas in high yields per pass, and development of new processes for producing selected higher-value products. A general goal is to develop improved understanding of catalytic reaction mechanisms for these processes. Research topics that will be investigated by the CFFLS to achieve these goals are briefly summarized below along product lines. Transportation fuel Ø Technology will be developed for conversion of methanol to a number of oxygenated compounds that should make excellent diesel fuel and diesel fuel additives. We will attempt to find catalysts and operating conditions for Fischer-Tropsch processes that yield more oxygenated products than are now made using conventional FT catalysts. This program will emphasize oxygenated compounds that are stable liquids at ambient conditions such as methylal, dimethylacetal, dioxolane, dimethyl dioxolane, dimethyl carbonate, and ethylene glycol. Ø Research will be conducted on the conversion of methanol to higher ethers (C5 - C7) and alcohols (C4 - C6). Such ethers and alcohols can be used as additives to improve the performance of gasoline and diesel fuel. Ø Processes to produce dimethyl carbonate (DMC) by reaction of methanol with urea will be explored. The oxidative carbonylation of methanol to yield DMC will be investigated. Ø The hydroprocessing of the C12 - C60 Fischer-Tropsch fraction to produce low pour-point, high cetane, diesel fuel, jet fuel, and lubricating oil will be investigated. Ø The conversion of methanol to olefins, and subsequently into diesel fuel and gasoline (MOGD) using new molecular sieve catalysts will be investigated. Synthesis gas Ø The conversion of natural gas to syngas by reaction with carbon dioxide will be investigated. This program will emphasize the development of more active and economical catalysts that resist carbon deposition. Both pure CO2 and mixtures of CO2 and H2O will be used in the reforming reactions. The reaction of CO2 with other hydrocarbons will also be examined. Benefits of the resulting technology will include utilization of CO2, production of syngas with tailored CO/H2 ratios, and development of processing conditions suitable for oil fields emitting gas that contains both CH4 and CO2. Hydrogen Ø Novel methods of producing hydrogen will be investigated, including catalytic decomposition of methane or other hydrocarbons and redox cycling of binary metal oxides. Ø Development of water-gas shift catalysts that are more active at lower temperatures. Ø Catalytic reforming of methanol to hydrogen and carbon dioxide. Methanol Ø The combined synthesis of methanol and dimethyl ether from syngas at lower temperatures (80-100 °C) than currently used (250 °C) will be investigated. The use of lower temperatures should increase conversion of syngas to methanol per pass. Advanced Analytic Characterization Research Ø A wide range of advanced analytical techniques will be employed to obtain accurate determinations of both product distribution and catalyst structure and reactions. These techniques include TGA/GC-MS, NMR using 13C and other nuclei, x-ray absorption fine structure (XAFS) spectroscopy, Mössbauer spectroscopy, HPLC, TEM, computer-controlled SEM, XRD, FTIR, ESR, XPS and other methods. In situ analytical measurements at elevated temperatures and pressures will be emphasized. | |
Project Background | |
Faculty and students from five universities (Kentucky, West Virginia, Utah, Pittsburgh and Auburn) are collaborating on a basic research program to develop novel C1chemistry processes for the production of clean, high quality transportation fuel. An Industrial Advisory Board (IAB) with members from Chevron, Eastman Chemical, Energy International, Teir Associates, and the Department of Defense has been formed to provide practical guidance to the program. The program has two principal objectives. 1. Develop technology for conversion of C1 source materials (natural gas, synthesis gas, carbon dioxide and monoxide, and methanol) into clean, high efficiency transportation fuel. 2. Develop novel processes for producing hydrogen from natural gas and other hydrocarbons. Transportation fuel Ø Technology will be developed for conversion of methanol to a number of oxygenated compounds that should make excellent diesel fuel and diesel fuel additives. We will attempt to find catalysts and operating conditions for Fischer-Tropsch processes that yield more oxygenated products than are now made using conventional FT catalysts. This program will emphasize oxygenated compounds that are stable liquids at ambient conditions such as methylal, dimethylacetal, dioxolane, dimethyl dioxolane, dimethyl carbonate, and ethylene glycol. Ø Research will be conducted on the conversion of methanol to higher ethers (C5 - C7) and alcohols (C4 - C6). Such ethers and alcohols can be used as additives to improve the performance of gasoline and diesel fuel. Ø Processes to produce dimethyl carbonate (DMC) by reaction of methanol with urea will be explored. The oxidative carbonylation of methanol to yield DMC will be investigated. Ø The hydroprocessing of the C12 - C60 Fischer-Tropsch fraction to produce low pour-point, high cetane, diesel fuel, jet fuel, and lubricating oil will be investigated. Ø The conversion of methanol to olefins, and subsequently into diesel fuel and gasoline (MOGD) using new molecular sieve catalysts will be investigated. Synthesis gas Ø The conversion of natural gas to syngas by reaction with carbon dioxide will be investigated. This program will emphasize the development of more active and economical catalysts that resist carbon deposition. Both pure CO2 and mixtures of CO2 and H2O will be used in the reforming reactions. The reaction of CO2 with other hydrocarbons will also be examined. Benefits of the resulting technology will include utilization of CO2, production of syngas with tailored CO/H2 ratios, and development of processing conditions suitable for oil fields emitting gas that contains both CH4 and CO2. Hydrogen Ø Novel methods of producing hydrogen will be investigated, including catalytic decomposition of methane or other hydrocarbons and redox cycling of binary metal oxides. Ø Development of water-gas shift catalysts that are more active at lower temperatures. Ø Catalytic reforming of methanol to hydrogen and carbon dioxide. Methanol Ø The combined synthesis of methanol and dimethyl ether from syngas at lower temperatures (80-100 °C) than currently used (250 °C) will be investigated. The use of lower temperatures should increase conversion of syngas to methanol per pass. Advanced Analytic Characterization Research Ø A wide range of advanced analytical techniques will be employed to obtain accurate determinations of both product distribution and catalyst structure and reactions. These techniques include TGA/GC-MS, NMR using 13C and other nuclei, x-ray absorption fine structure (XAFS) spectroscopy, Mössbauer spectroscopy, HPLC, TEM, computer-controlled SEM, XRD, FTIR, ESR, XPS and other methods. In situ analytical measurements at elevated temperatures and pressures will be emphasized. | |
Project Milestones | |
This information is currently unavailable. | |
Project Accomplishments | |
Title: | 20001 annual report |
Date: | 04/19/2002 |
Description | The addition of acetylenic compounds in Fischer-Tropsch synthesis is found to produce significant amounts of oxygenated products in FT diesel fuels. Such oxygenated products should decrease particulate matter (PM) emissions. Nanoscale, binary, Fe-based catalysts supported on alumina have been shown to have significant activity for the decomposition of methane into pure hydrogen and potentially valuable multi-walled carbon nanotubes. Catalytic synthesis processes have been developed for synthesis of diethyl carbonate, higher ethers, and higher alcohols from C1 source materials. Testing of the effect of adding these oxygenates to diesel fuel on PM emissions has begun using a well-equipped small diesel engine test facility. Supercritical fluid (SCF) FT synthesis has been conducted under SCF hexane using both Fe and Co catalysts. There is a marked effect on the hydrocarbon product distribution, with a shift to higher carbon number products. |
Title: | semianual briefing 10/1/2001 |
Date: | 02/08/2002 |
Description | see images |
- Details
Thursday, a workshop explored the industry's future in both countries. It represents a partnership between the two countries, but also with the public and private sectors.
They're working toward reducing carbon emissions while keeping the lights on.
"In China, 70 percent of energy comes from coal," said Qinyung Sun, West Virginia's Assistant for China Affairs. "In the states, about 50 percent of electricity comes from coal. You know, in our state, not only employment, economics, education, everything relies on coal. That's why these similarities brought us together."
The partnership has been in the works for several years in government and business.
"As we look at what's going on into the future, we are seriously challenged by the way of using coal in a way that is environmentally sound and politically acceptable, socially acceptable," said Jerry Fletcher, the director of the U.S. - China Energy Center.
Presentations showed how energy companies in both countries are pushing the boundaries of coal technology, from coal to liquids, gasification, and even using excess carbon dioxide to farm algae for liquid fuels.
China recently announced their goal of reducing carbon emission per unit of gross domestic product between 40 percent to 45 percent from their levels in 2005 within the next 10 years, as one of the day's speakers referenced.
"One of the fascinating things about listening to the Chinese business people, government people is just to see the scope and scale of their development, and what's going on there," said Frank Palmer, with U.S.-based Peabody Energy.
There is also a lot of work going on in the United States, thanks to support from the government.
In a statement by Sen. Robert C. Byrd read at the workshop, he said:
"Together, our nations can tackle the problems of global climate change while making use of our abundant and secure domestic energy resources. However, if we do not adequately invest in the research and development needed to address these challenges in the coming decade; the environmental and financial costs will be enormous."
"We think it's possible," Fletcher said. "We know the technology is there, but it's going to take a great deal of time and a great deal of investment to bring it to fruition."
The conference continued Friday, with a look at ways governments and businesses can work together on moving technology and policy forward."
All the obligatory caveats were made, of course, with the required genuflections towards environmental consciousness and timorous economic conservatism . But, the essence of coal conversion industry is distilled in the words of Dr. Flethcher:
