Abstract: A process for converting carbonaceous materials or light hydrocarbon gases into products comprising predominately C5+ hydrocarbons. The process converts the feedstock into synthesis gas comprising hydrogen and carbon monoxide and then uses the Fischer-Tropsch reaction to produce heavy hydrocarbons. A small excess of hydrogen is produced in the syngas generator or by water gas shift for use in product upgrading and for blending with Fischer-Tropsch tail gas for recycle back to syngas generation. A portion of the Fischer-Tropsch tail gas is used as fuel, thus purging combustible light gases and CO2 from the tail gas. Hydrogen rich purge gas is blended into the remaining tail gas resulting in a recycle stream that is returned to the syngas generator. The tail gas components are therefore efficiently used to produce more products.

Abstract: A process for producing transportation fuels, such as gasoline and diesel fuel, from syngas with a low H2/CO ratio. The syngas is first converted to dimethyl ether which is then converted to gasoline by way of a dimethyl ether to gasoline process and to diesel fuel by way of a Fischer-Tropsch process.

Abstract: A process for producing transportation fuels, such as gasoline and diesel fuel, from syngas with a low H2/CO ratio. The syngas is first converted to dimethyl ether which is then converted to gasoline by way of a dimethyl ether to gasoline process and to diesel fuel by way of a Fischer-Tropsch process.

Abstract: TNT and nitramines, such as RDX, are recovered from mixtures containing same. The present invention more particularly relates to the removal of such mixtures from munitions and the separation of components contained in the munitions.

Abstract: A continuous process for the separate recovery of TNT and RDX from a mixture of TNT and RDX. The mixture is introduced into a first vessel wherein TNT is separated from the RDX by use of a solvent that is effective for dissolving TNT but not RDX. The TNT in solvent is passed to a separation stage wherein the solvent is recovered a recycled to the first vessel. A slurry of RDX and water are passed to a second vessel where the water is displaced with a desensitizing agent for desensitizing RDX.

Abstract: A process for accessing and defusing munitions using fluid jet technology containing abrasive material and recovering the abrasive. The explosive material can also be removed from the munition casing by fluid jet technology, after the munition has been defused.

Abstract: A process for regenerating a slurry Fischer-Tropsch catalyst, which needs regeneration, involves de-waxing and drying the catalyst sufficiently to produce a free-flowing catalyst powder that is fluidizable; fluidizing the catalyst powder; treating the catalyst powder with an oxygen treatment; reducing the catalyst powder with a reducing gas to form a reduced catalyst powder; and mixing the reduced catalyst powder with hydrocarbons to form a regenerated, slurry catalyst. The oxidation and reduction steps may be repeated. An oxygen treatment includes using a fixed O2 level with ramped temperatures, fixed temperatures with increased O2 levels, or a combination.

Abstract: A Fischer-Tropsch catalyst for the conversion of synthesis gas into Fischer-Tropsch products includes a stationary Fischer-Tropsch catalyst having a voidage ratio greater than approximately 0.45 or 0.6 and may further have a catalyst concentration for a given reactor volume of at least 10 percent. A Fischer-Tropsch catalyst has a structured shape promoting non-Taylor flow and/or producing a productivity in the range of 200-4000 vol CO/vol. Catalyst/hour or greater over at least a 600 hour run of a Fischer-Tropsch reactor with the catalyst therein. A system for converting synthesis gas into longer-chain hydrocarbon products through the Fisher-Tropsch reaction has a reactor for receiving synthesis gas directly or as a saturated hydrocarbon liquid or a combination, and a stationary, structured Fischer-Tropsch catalyst disposed within the reactor for converting at least a portion of the synthesis gas into longer-chain hydrocarbons through Fischer-Tropsch reaction.

Abstract: A solvent extraction process for the separation recovery of TNT and RDX from Composition B-containing munitions. The munitions also contain liner materials, such as asphalt and binders, and sealers, such as wax, each of which are also recovered by use of solvent technology.

Abstract: A process for regenerating a slurry Fischer-Tropsch catalyst, which needs regeneration, involves de-waxing and drying the catalyst sufficiently to produce a free-flowing catalyst powder that is fluidizable; fluidizing the catalyst powder; treating the catalyst powder with an oxygen treatment; reducing the catalyst powder with a reducing gas to form a reduced catalyst powder; and mixing the reduced catalyst powder with hydrocarbons to form a regenerated, slurry catalyst. The oxidation and reduction steps may be repeated. An oxygen treatment includes using a fixed O2 level with ramped temperatures, fixed temperatures with increased O2 levels, or a combination.

Abstract: A process and apparatus for synthesizing hydrocarbons from synthesis gas is disclosed. The process useful for initial start-up of a Fischer-Tropsch reactor system in a slurry bubble column reactor. Synthesis gas comprising hydrogen and carbon dioxide is reacted to form hydrocarbons. A liquid slurry comprising a start-up composition may include polyalpha olefins, astor wax, waxes, and paraffins. The reaction employs a low superficial vapor velocity, a medium to high catalyst concentration, and relatively mild reactor temperatures as compared to conventional Fischer-Tropsch processes.

Abstract: A system and method of operating a pre-reformer in a gas-to-liquids plant at minimum steam/carbon levels in order to reduce the C2+ content is provided that allows for the efficient production of synthesis gas to be used in producing liquid hydrocarbons preferably through a Fischer-Tropsch synthesis. The process and system involves providing steam, natural gas having greater than 3 percent C2+, and possibly hydrogen to a pre-reformer and converting a significant amount of the C2+ to methane and CO2 and then using a synthesis gas generator to prepare a synthesis gas feedstock with about a 2:1 H2:CO ratio and without undue soot formation. The synthesis gas is used in a Fischer-Tropsch synthesis unit to convert the synthesis gas to the heavier hydrocarbons. Water, light hydrocarbons, and portions of the tail gas may be recycled in different embodiments.

Abstract: A method for hydrocarbon synthesis reactions from carbon monoxide and hydrogen using a catalyst pellet which includes a solid core and a coated layer of porous support impregnated with a catalyst which optimizes the CO conversion.

Abstract: A Fischer-Tropsch catalyst for the conversion of synthesis gas into Fischer-Tropsch products includes a stationary Fischer-Tropsch catalyst having a voidage ratio greater than approximately 0.45 or 0.6 and may further have a catalyst concentration for a given reactor volume of at least 10 percent. A Fischer-Tropsch catalyst has a structured shape promoting non-Taylor flow and/or producing a productivity in the range of 200-4000 vol CO/vol. Catalyst/hour or greater over at least a 600 hour run of a Fischer-Tropsch reactor with the catalyst therein. A system for converting synthesis gas into longer-chain hydrocarbon products through the Fisher-Tropsch reaction has a reactor for receiving synthesis gas directly or as a saturated hydrocarbon liquid or a combination, and a stationary, structured Fischer-Tropsch catalyst disposed within the reactor for converting at least a portion of the synthesis gas into longer-chain hydrocarbons through Fischer-Tropsch reaction.

Abstract: A process for the conversion of a picrate salt, preferably ammonium pricrate, to picric acid by acidifying the picrate salt in a two phase liquid system. One phase is an aqueous phase which contains an acid which is effective for acidifying ammonium picrate to picric acid and the other phase is an organic solvent phase in which the picric acid is soluble.

Abstract: A Fischer-Tropsch catalyst for the conversion of synthesis gas into Fischer-Tropsch products includes a stationary Fischer-Tropsch catalyst having a voidage ratio greater than approximately 0.45 or 0.6 and may further have a catalyst concentration for a given reactor volume of at least 10 percent. A Fischer-Tropsch catalyst has a structured shape promoting non-Taylor flow and/or producing a productivity in the range of 200-4000 vol CO/vol. Catalyst/hour or greater over at least a 600 hour run of a Fischer-Tropsch reactor with the catalyst therein. A system for converting synthesis gas into longer-chain hydrocarbon products through the Fisher-Tropsch reaction has a reactor for receiving synthesis gas directly or as a saturated hydrocarbon liquid or a combination, and a stationary, structured Fischer-Tropsch catalyst disposed within the reactor for converting at least a portion of the synthesis gas into longer-chain hydrocarbons through Fischer-Tropsch reaction.

Abstract: A process for the conversion of a picrate salt, preferably ammonium pricrate, to picric acid by acidifying the picrate salt in a two phase liquid system. One phase is an aqueous phase which contains an acid which is effective for acidifying ammonium picrate to picric acid and the other phase is an organic solvent phase in which the picric acid is soluble.

Abstract: Ammonium picrate, Explosive "D", is converted to picric acid, which is then converted to triaminophenol by the conversion of the aromatic nitro groups to amino groups. The triaminophenols are then converted to triaminobenzenes by the removal of the hydroxyl groups and the triaminobenzenes are converted to m-phenylenediamine, aniline, and primary aliphatic amines by the removal of amino groups.

Abstract: A supported particulate cobalt catalyst is formed by dispersing cobalt, alone or with a metal promoter, particularly rhenium, as a thin catalytically active film upon a particulate support, especially a silica or titania support. This catalyst can be used to convert an admixture of carbon monoxide and hydrogen to a distillate fuel constituted principally of an admixture of linear paraffins and olefins, particularly a C.sub.10+ distillate, at high productivity, with low methane selectivity. A process is also disclosed for the preparation of these catalysts.

Abstract: A supported particulate cobalt catalyst is formed by dispersing cobalt, alone or with a metal promoter, particularly rhenium, as a thin catalytically active film upon a particulate support, especially a silica or titania support. This catalyst can be used to convert an admixture of carbon monoxide and hydrogen to a distillate fuel constituted principally of an admixture of linear paraffins and olefins, particularly a C10+ distillate, at high productivity, with low methane selectivity. A process is also disclosed for the preparation of these catalysts.