Interactive chemistry of coal-petroleum processing: Quarterly progress report, September 15, 1987-December 15, 1987
Technical Report
·
OSTI ID:5330476
Some conversion and hydrogenation reactivity of benzofuran was observed in the thermal reaction with sulfur. However, catalytic reaction with Mo naphthenate was required for substantial, nearly 50%, hydrogenation, complete hydrogenolysis and high levels, approx.80%, deoxygenation. The introduction of benzothiophene and o-cresol lowered both hydrogenation and deoxygenation while the addition of quinoline markedly reduced hydrogenation, virtually eliminated deoxygenation and slightly reduced hydrogenolysis. Quinoline, by contrast to all of the other compounds studied, produced substantial thermal hydrogenation to THQ; however, the introduction of both hydrocarbons and heteroatomics reduced the conversion of quinoline to THQ. The presence of the oxygen containing compounds nearly eliminated the conversion of quinoline to THQ. Similar results were observed in the thermal reactions with sulfur. Catalytically, quinoline was readily hydrogenated and denitrogenated. The addition of both hydrocarbons and heteroatomics had little influence on the quinoline reaction except for the introduction of benzothiophene at higher reactant levels. When added to a catalytic reaction of naphthalene and quinoline, the addition of benzothiophene reduced the catalyst poisoning effects of quinoline. The hydrogenation of naphthalene double while the hydrogenation, hydrogenolysis and denitrogenation of quinoline were all improved. 15 refs.
- Research Organization:
- Auburn Univ., AL (USA). Dept. of Chemical Engineering
- DOE Contract Number:
- FG22-85PC80502
- OSTI ID:
- 5330476
- Report Number(s):
- DOE/PC/80502-T8; ON: DE88004541
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
01 COAL, LIGNITE, AND PEAT
010405* -- Coal
Lignite
& Peat-- Hydrogenation & Liquefaction
AROMATICS
AZAARENES
AZINES
BENZOFURANS
CARBONACEOUS MATERIALS
CATALYSTS
CATALYTIC EFFECTS
CHALCOGENIDES
CHEMICAL REACTION YIELD
CHEMICAL REACTIONS
CHEMISTRY
CHROMATOGRAPHY
COAL
CONDENSED AROMATICS
COPROCESSING
CRESOLS
DENITRIFICATION
DESULFURIZATION
DOCUMENT TYPES
ELEMENTS
ENERGY SOURCES
FOSSIL FUELS
FUELS
FURANS
GAS CHROMATOGRAPHY
HETEROCYCLIC COMPOUNDS
HYDROCARBONS
HYDROGEN COMPOUNDS
HYDROGEN SULFIDES
HYDROGENATION
HYDROXY COMPOUNDS
INDAN
INDENE
MATERIALS
METALS
MOLYBDENUM
NAPHTHALENE
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
PETROLEUM
PHENOLS
PROCESSING
PROGRESS REPORT
PYRIDINES
QUINOLINES
SEPARATION PROCESSES
STRUCTURAL MODELS
SULFIDES
SULFUR COMPOUNDS
THIONAPHTHENES
TRANSITION ELEMENTS
YIELDS
010405* -- Coal
Lignite
& Peat-- Hydrogenation & Liquefaction
AROMATICS
AZAARENES
AZINES
BENZOFURANS
CARBONACEOUS MATERIALS
CATALYSTS
CATALYTIC EFFECTS
CHALCOGENIDES
CHEMICAL REACTION YIELD
CHEMICAL REACTIONS
CHEMISTRY
CHROMATOGRAPHY
COAL
CONDENSED AROMATICS
COPROCESSING
CRESOLS
DENITRIFICATION
DESULFURIZATION
DOCUMENT TYPES
ELEMENTS
ENERGY SOURCES
FOSSIL FUELS
FUELS
FURANS
GAS CHROMATOGRAPHY
HETEROCYCLIC COMPOUNDS
HYDROCARBONS
HYDROGEN COMPOUNDS
HYDROGEN SULFIDES
HYDROGENATION
HYDROXY COMPOUNDS
INDAN
INDENE
MATERIALS
METALS
MOLYBDENUM
NAPHTHALENE
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
PETROLEUM
PHENOLS
PROCESSING
PROGRESS REPORT
PYRIDINES
QUINOLINES
SEPARATION PROCESSES
STRUCTURAL MODELS
SULFIDES
SULFUR COMPOUNDS
THIONAPHTHENES
TRANSITION ELEMENTS
YIELDS