Catalysts possessing augmented C-O and C-N hydrogenolysis activity: Final progress report, August 1, 1983--July 31, 1987
Technical Report
·
OSTI ID:6944963
The objective of this project is to synthesize and investigate new sulfided catalyst systems having higher carbon-heteroatom hydrogenolysis activity as compared to ring hydrogenation activity. A fundamental approach is applied to gain understanding of the basic catalytic properties which relate to hydrogenolysis and hydrogenation functions of the catalysts. This involves preparation of new catalysts, characterization of their properties, and model compound reactivity studies. Selected catalysts are applied in studies of more complex O- and N-containing model compounds with the objective of providing fundamental data on the stereochemistry of hydrogenation, HDO and HDN reactions. These data are used to develop steric surface-reactant models for sulfided catalysts. This knowledge could be reasonably expected to allow for tailoring of selective sulfided catalysts possessing augmented C-O and C-N hydrogenolysis activity. Such new catalysts should be of particular importance for upgrading of coal-derived liquids and solids, as well as other heavy feedstocks. Research is divided into four tasks: A--catalyst preparation and activity testing; B--catalyst characterization; C--catalyst activity and functional selectivity under hydroprocessing conditions; and D--stereochemical studies. Results are discussed. 30 refs., 15 figs., 16 tabs.
- Research Organization:
- Utah Univ., Salt Lake City (USA). Dept. of Fuels Engineering
- DOE Contract Number:
- FG22-83PC60812
- OSTI ID:
- 6944963
- Report Number(s):
- DOE/PC/60812-T6; ON: DE88011256
- Country of Publication:
- United States
- Language:
- English
Similar Records
Catalysts possessing augmented C-O and C-N hydrogenolysis activity. Progress report No. 2, January-March 1984
Catalysts possessing augmented C-O and C-N hydrogenolysis activity. Progress report No. 3, April-June 1984
Catalysts possessing augmented C-O and C-N hydrogenolysis activity. Progress report No. 4, July-September 1984
Technical Report
·
Sun Apr 08 23:00:00 EST 1984
·
OSTI ID:6024456
Catalysts possessing augmented C-O and C-N hydrogenolysis activity. Progress report No. 3, April-June 1984
Technical Report
·
Sun Jul 01 00:00:00 EDT 1984
·
OSTI ID:6221190
Catalysts possessing augmented C-O and C-N hydrogenolysis activity. Progress report No. 4, July-September 1984
Technical Report
·
Mon Oct 01 00:00:00 EDT 1984
·
OSTI ID:6254927
Related Subjects
090121 -- Hydrocarbon Fuels-- Chemical Synthesis-- (1976-1989)
10 SYNTHETIC FUELS
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
AROMATICS
AZAARENES
AZOLES
CATALYST SUPPORTS
CATALYSTS
CATALYTIC EFFECTS
CHEMICAL PREPARATION
CHEMICAL REACTION KINETICS
CHEMICAL REACTION YIELD
CHEMICAL REACTIONS
COBALT
COMPARATIVE EVALUATIONS
CONDENSED AROMATICS
DOCUMENT TYPES
ELEMENTS
FURANS
HETEROCYCLIC COMPOUNDS
HYDROCARBONS
HYDROGENATION
INDOLES
IRIDIUM
KINETICS
METALS
MOLYBDENUM
NAPHTHALENE
NICKEL
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
PALLADIUM
PLATINUM
PLATINUM METALS
PROGRESS REPORT
PYRROLES
REACTION KINETICS
RHENIUM
RHODIUM
RUTHENIUM
SPECIFICITY
STEREOCHEMISTRY
SULFIDATION
SYNTHESIS
THIOPHENE
TRANSITION ELEMENTS
YIELDS
10 SYNTHETIC FUELS
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
AROMATICS
AZAARENES
AZOLES
CATALYST SUPPORTS
CATALYSTS
CATALYTIC EFFECTS
CHEMICAL PREPARATION
CHEMICAL REACTION KINETICS
CHEMICAL REACTION YIELD
CHEMICAL REACTIONS
COBALT
COMPARATIVE EVALUATIONS
CONDENSED AROMATICS
DOCUMENT TYPES
ELEMENTS
FURANS
HETEROCYCLIC COMPOUNDS
HYDROCARBONS
HYDROGENATION
INDOLES
IRIDIUM
KINETICS
METALS
MOLYBDENUM
NAPHTHALENE
NICKEL
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
PALLADIUM
PLATINUM
PLATINUM METALS
PROGRESS REPORT
PYRROLES
REACTION KINETICS
RHENIUM
RHODIUM
RUTHENIUM
SPECIFICITY
STEREOCHEMISTRY
SULFIDATION
SYNTHESIS
THIOPHENE
TRANSITION ELEMENTS
YIELDS