|
|
|
|
LEADER |
00000nam a22000003u 4500 |
001 |
b7627985 |
003 |
CoU |
005 |
20130730223208.6 |
006 |
m o d f |
007 |
cr ||||||||||| |
008 |
141106e19830901||| ot f0|||||eng|d |
035 |
|
|
|a (TOE)ost5722090
|
035 |
|
|
|a (TOE)5722090
|
040 |
|
|
|a TOE
|c TOE
|
049 |
|
|
|a GDWR
|
072 |
|
7 |
|a 01
|2 edbsc
|
086 |
0 |
|
|a E 1.99:ornl/tm-8662
|
086 |
0 |
|
|a E 1.99:ornl/tm-8662
|
088 |
|
|
|a ornl/tm-8662
|
245 |
0 |
0 |
|a Studies of the effect of selected nondonor solvents on coal liquefaction yields
|h [electronic resource]
|
260 |
|
|
|a Oak Ridge, Tenn. :
|b Oak Ridge National Laboratory. ;
|a Oak Ridge, Tenn. :
|b distributed by the Office of Scientific and Technical Information, U.S. Department of Energy,
|c 1983.
|
300 |
|
|
|a Pages: 130 :
|b digital, PDF file.
|
336 |
|
|
|a text
|b txt
|2 rdacontent.
|
337 |
|
|
|a computer
|b c
|2 rdamedia.
|
338 |
|
|
|a online resource
|b cr
|2 rdacarrier.
|
500 |
|
|
|a Published through SciTech Connect.
|
500 |
|
|
|a 09/01/1983.
|
500 |
|
|
|a "ornl/tm-8662"
|
500 |
|
|
|a "DE83017069"
|
500 |
|
|
|a Jolley, R. L.; Rodgers, B. R.; Benjamin, B. M.; Poutsma, M. L.; Douglas, E. C.; McWhirter, D. A.
|
520 |
3 |
|
|a The objective of this research program was to evaluate the effectiveness of selected nondonor solvents (i.e., solvents that are not generally considered to have hydrogen available for hydrogenolysis reactions) for the solubilization of coals. Principal criteria for selection of candidate solvents were that the compound should be representative of a major chemical class, should be present in reasonable concentration in coal liquid products, and should have the potential to participate in hydrogen redistribution reactions. Naphthalene, phenanthrene, pyrene, carbazole, phenanthridine, quinoline, 1-naphthol, and diphenyl ether were evaluated to determine their effect on coal liquefaction yields and were compared with phenol and two high-quality process solvents, Wilsonville SRC-I recycle solvent and Lummus ITSL heavy oil solvent. The high conversion efficacy of 1-naphthol may be attributed to its condensation to binaphthol and the consequent availability of hydrogen. The effectiveness of both the nitrogen heterocycles and the polycyclic aromatic hydrocarbon (PAH) compounds may be due to their polycyclic aromatic nature (i.e., possible hydrogen shuttling or transfer agents) and their physical solvent properties. The relative effectiveness for coal conversion of the Lummus ITSL heavy oil solvent as compared with the Wilsonville SRC-I process solvent may be attributed to the much higher concentration of 3-, 4-, and 5-ring PAH and hydroaromatic constituents in Lummus solvent. The chemistry of coal liquefaction and the development of recycle, hydrogen donor, and nondonor solvents are reviewed. The experimental methodology for tubing-bomb tests is outlined, and experimental problem areas are discussed.
|
536 |
|
|
|b W-7405-ENG-26.
|
650 |
|
7 |
|a Carbazoles.
|2 local.
|
650 |
|
7 |
|a Comparative Evaluations.
|2 local.
|
650 |
|
7 |
|a Chemical Bonds.
|2 local.
|
650 |
|
7 |
|a Cleavage.
|2 local.
|
650 |
|
7 |
|a Coal.
|2 local.
|
650 |
|
7 |
|a Depolymerization.
|2 local.
|
650 |
|
7 |
|a Coal Liquefaction.
|2 local.
|
650 |
|
7 |
|a Organic Solvents.
|2 local.
|
650 |
|
7 |
|a Yields.
|2 local.
|
650 |
|
7 |
|a Ethers.
|2 local.
|
650 |
|
7 |
|a Naphthalene.
|2 local.
|
650 |
|
7 |
|a Naphthols.
|2 local.
|
650 |
|
7 |
|a Recycling.
|2 local.
|
650 |
|
7 |
|a Phenanthrene.
|2 local.
|
650 |
|
7 |
|a Pyrene.
|2 local.
|
650 |
|
7 |
|a Quinolines.
|2 local.
|
650 |
|
7 |
|a Catalysts.
|2 local.
|
650 |
|
7 |
|a Chemical Reaction Kinetics.
|2 local.
|
650 |
|
7 |
|a Dissolution.
|2 local.
|
650 |
|
7 |
|a Experimental Data.
|2 local.
|
650 |
|
7 |
|a Organic Nitrogen Compounds.
|2 local.
|
650 |
|
7 |
|a Phenols.
|2 local.
|
650 |
|
7 |
|a Polycyclic Aromatic Hydrocarbons.
|2 local.
|
650 |
|
7 |
|a Radicals.
|2 local.
|
650 |
|
7 |
|a Aromatics.
|2 local.
|
650 |
|
7 |
|a Azines.
|2 local.
|
650 |
|
7 |
|a Azoles.
|2 local.
|
650 |
|
7 |
|a Carbonaceous Materials.
|2 local.
|
650 |
|
7 |
|a Chemical Reactions.
|2 local.
|
650 |
|
7 |
|a Condensed Aromatics.
|2 local.
|
650 |
|
7 |
|a Crystal Structure.
|2 local.
|
650 |
|
7 |
|a Data.
|2 local.
|
650 |
|
7 |
|a Decomposition.
|2 local.
|
650 |
|
7 |
|a Fossil Fuels.
|2 local.
|
650 |
|
7 |
|a Fuels.
|2 local.
|
650 |
|
7 |
|a Heterocyclic Compounds.
|2 local.
|
650 |
|
7 |
|a Hydrocarbons.
|2 local.
|
650 |
|
7 |
|a Hydroxy Compounds.
|2 local.
|
650 |
|
7 |
|a Information.
|2 local.
|
650 |
|
7 |
|a Kinetics.
|2 local.
|
650 |
|
7 |
|a Liquefaction.
|2 local.
|
650 |
|
7 |
|a Materials.
|2 local.
|
650 |
|
7 |
|a Microstructure.
|2 local.
|
650 |
|
7 |
|a Numerical Data.
|2 local.
|
650 |
|
7 |
|a Organic Compounds.
|2 local.
|
650 |
|
7 |
|a Organic Oxygen Compounds.
|2 local.
|
650 |
|
7 |
|a Pyridines.
|2 local.
|
650 |
|
7 |
|a Energy Sources.
|2 local.
|
650 |
|
7 |
|a Solvents.
|2 local.
|
650 |
|
7 |
|a Reaction Kinetics.
|2 local.
|
650 |
|
7 |
|a Thermochemical Processes.
|2 local.
|
650 |
|
7 |
|a Coal, Lignite, And Peat.
|2 edbsc.
|
710 |
2 |
|
|a Oak Ridge National Laboratory.
|4 res.
|
710 |
1 |
|
|a United States.
|b Department of Energy.
|b Office of Scientific and Technical Information.
|4 dst.
|
856 |
4 |
0 |
|u http://www.osti.gov/servlets/purl/5722090/
|z Online Access
|
907 |
|
|
|a .b76279856
|b 03-07-23
|c 12-11-13
|
998 |
|
|
|a web
|b 12-11-13
|c f
|d m
|e p
|f eng
|g
|h 0
|i 3
|
956 |
|
|
|a Information bridge
|
999 |
f |
f |
|i a0101b86-0302-5f75-afaf-c1e0316eb501
|s 2450178c-1f12-5e7f-82d9-e65a47dc99ec
|
952 |
f |
f |
|p Can circulate
|a University of Colorado Boulder
|b Online
|c Online
|d Online
|e E 1.99:ornl/tm-8662
|h Superintendent of Documents classification
|i web
|n 1
|