Role of the hydrogen-donor solvent in coal hydroliquefaction. Progress report, September 1, 1979-November 30, 1980
The principal disproportionation products of 1,2-dihydronaphthalene (1,2-DHN) are naphthalene (Nap) and tetralin (Tet). Dimers of 1,2-DHN constitute 17% and 5% of the respective liquid phase (285 to 315/sup 0/C) and gas phase (385 to 410/sup 0/C) products. The Nap:Tet ratio is one in the presence of solvents, but is > 1 and < 2 in their absence. Gas phase reaction kinetics indicate that 1,2-DHN disappears by simultaneous first and second order reactions. These results are consistent with a concerted second order disappearance of 1,2-DHN to produce equal amounts of Nap and Tet, accompanied by either carbonium ion or free radical side reactions that produce more Nap than Tet, together with 1,2-DHN dimers. Preliminary evaluation of the liquid phase kinetics suggest they follow a similar pattern. The structures of the dimers should reveal whether they were formed by a carbonium ion or free radical mechanism. Isolation of the dimers will be attempted by preparative GC (PGC) followed by TLC to remove thermal decomposition products formed during PGC. Exploratory results suggest that heating 1,2-DHN (300/sup 0/C) in the presence of tetraphenylethane, which dissociates into diphenylmethyl radicals, may constitute a model for the free radical conversion of 1,2-DHN into Nap during coal hydroliquefaction. Further studies of this system will be conducted.
- Research Organization:
- Weber State Coll., Ogden, UT (USA)
- DOE Contract Number:
- AC02-79ER10510
- OSTI ID:
- 6892949
- Report Number(s):
- DOE/ER/10510-T2
- Country of Publication:
- United States
- Language:
- English
Similar Records
Role of the hydrogen donor solvent in coal hydroliquefaction. Progress report, December 1, 1980-February 28, 1982
Products, radical intermediates, and hydrogen atom production in the thermal decomposition of 1,2-dihydronaphthalene
Thermochemistry and product studies of the isomerization and cracking of hydroaromatic molecules and the reactions of hydrogen atom produced from radical oxidation intermediates of hydroaromatic molecules. [1, 2 dihydronapthalene]
Technical Report
·
Thu Oct 15 00:00:00 EDT 1981
·
OSTI ID:5858374
Products, radical intermediates, and hydrogen atom production in the thermal decomposition of 1,2-dihydronaphthalene
Journal Article
·
Wed Oct 03 00:00:00 EDT 1984
· J. Am. Chem. Soc.; (United States)
·
OSTI ID:6313623
Thermochemistry and product studies of the isomerization and cracking of hydroaromatic molecules and the reactions of hydrogen atom produced from radical oxidation intermediates of hydroaromatic molecules. [1, 2 dihydronapthalene]
Conference
·
Fri Dec 31 23:00:00 EST 1982
·
OSTI ID:5722058
Related Subjects
01 COAL, LIGNITE, AND PEAT
010405* -- Coal
Lignite
& Peat-- Hydrogenation & Liquefaction
AROMATICS
CATALYTIC EFFECTS
CHEMICAL REACTION KINETICS
CHEMICAL REACTIONS
CHLORIDES
CHLORINE COMPOUNDS
CHROMATOGRAPHY
COAL LIQUEFACTION
CONDENSED AROMATICS
DIMERS
GAS CHROMATOGRAPHY
HALIDES
HALOGEN COMPOUNDS
HYDROCARBONS
HYDROGEN TRANSFER
HYDROGENATION
KINETICS
LIQUEFACTION
MATHEMATICAL MODELS
NAPHTHALENE
ORGANIC COMPOUNDS
PURIFICATION
RADICALS
REACTION KINETICS
SEPARATION PROCESSES
TETRALIN
THERMOCHEMICAL PROCESSES
ZINC CHLORIDES
ZINC COMPOUNDS
ZINC HALIDES
010405* -- Coal
Lignite
& Peat-- Hydrogenation & Liquefaction
AROMATICS
CATALYTIC EFFECTS
CHEMICAL REACTION KINETICS
CHEMICAL REACTIONS
CHLORIDES
CHLORINE COMPOUNDS
CHROMATOGRAPHY
COAL LIQUEFACTION
CONDENSED AROMATICS
DIMERS
GAS CHROMATOGRAPHY
HALIDES
HALOGEN COMPOUNDS
HYDROCARBONS
HYDROGEN TRANSFER
HYDROGENATION
KINETICS
LIQUEFACTION
MATHEMATICAL MODELS
NAPHTHALENE
ORGANIC COMPOUNDS
PURIFICATION
RADICALS
REACTION KINETICS
SEPARATION PROCESSES
TETRALIN
THERMOCHEMICAL PROCESSES
ZINC CHLORIDES
ZINC COMPOUNDS
ZINC HALIDES