Abstract: A method is provided for introducing or reintroducing a gas into a slurry vessel holding a slurry comprising a liquid and solid particles and having a gas distributor for injecting a gas into the slurry, where the gas distributor includes a sparger device comprising an apertured sparger portion inside the slurry vessel, an inlet portion leading into the slurry vessel and an outlet portion leading from the slurry vessel, and a valve, external of the slurry vessel, operable to allow or deny flow from the sparger portion out through the outlet portion of the sparger device. The method comprises operating the valve to allow flow through the outlet portion of the sparger device, flushing the sparger device through the outlet portion to remove settled material which may be present in the sparger device, operating the valve to deny flow through the outlet portion of the sparger device, and introducing or reintroducing the gas into the slurry vessel through the sparger device.

Abstract: A process (10) for producing synthesis gas includes, in a gasification stage (12), gasifying a carbonaceous feestock to provide a raw synthesis gas which includes at least H2, CO and CH4 and, in a partial oxidation stage (14), subjecting the raw synthesis gas to partial oxidation in the presence of oxygen to provide an upgraded synthesis gas which includes less CH4 and more H2 and CO than the raw synthesis gas. The invention extends to a process for producing a synthesis gas derived product.

Abstract: A process for starting up a Fischer-Tropsch reactor includes establishing, in the reactor, an initial charge of molten wax. The initial reactor temperature is below the line-out reactor temperature but is sufficiently high for a Fischer-Tropsch reaction to take place. The reactor contains, in contact with the molten wax, at least a portion of its line-out catalyst inventory. Syngas is fed into the reactor at an initial flow rate below the line-out syngas flow rate. Initially a syngas H2:CO molar ratio is maintained at a higher value than its line-out value, whereafter the syngas H2:CO molar ratio is decreased to its line-out value. The syngas flow rate and the reactor temperature are then increased to their line-out values.

Abstract: A method of inhibiting erosion of an interior surface of a process vessel by solid objects carried in a fluid passing over the interior surface includes providing at least one formation at or in close proximity to the interior surface to interfere with the flow of the fluid over the interior surface, and to interfere with the movement of the solid objects by the fluid. The invention extends to a process vessel (10) which includes a body (16) defining an interior vessel surface (20), a catalyst bed (12) in the body (16), retaining means (22) on the catalyst bed for retaining the catalyst bed in position, and at least one formation (26) at or in close proximity to the interior vessel surface above the retaining means for interfering with fluid flow above the retaining means.

Abstract: A process for the production of hydrocarbons and ammonia, and more particularly a process for optimizing the production of hydrocarbons and ammonia using a combined hydrocarbon synthesis plant and ammonia synthesis plant. Synthesis gas exiting a reforming section of the hydrocarbon synthesis process is sent to a hydrogen extraction unit, where it is divided into a hydrogen-rich stream and a hydrogen-poor stream. The hydrogen-rich stream is then fed into an ammonia synthesis process. The hydrogen-poor stream may be returned to the hydrocarbon synthesis process or may be used as a fuel gas. The process reduces emission of CO2 into the atmosphere, and requires only one reforming section and one air separation unit for both processes. Removal of hydrogen from the hydrocarbon synthesis process before the synthesis gas enters a Fischer-Tropsch reactor also lowers the H2/CO ratio of the synthesis gas, therefore resulting in better hydrocarbon selectively.

Abstract: A process for preparing a cobalt based catalyst precursor includes, in a support impregnation stage, impregnating a coated catalyst support comprising porous catalyst support particles coated with carbon, with a cobalt salt, and partially drying the impregnated support. Thereafter, in a calcination stage, the partially dried impregnated support is calcined, to obtain the cobalt based catalyst precursor. The cobalt based catalyst precursor can then, in a reduction stage, be reduced to obtain a cobalt based Fischer-Tropsch catalyst.

Abstract: A method of treating an untreated catalyst support includes contacting an untreated catalyst support which is partially soluble in an aqueous acid and/or a neutral aqueous solution with a modifying component precursor of the formula Me(OR)x where Me is a modifying component selected from Si, Zr, Ti, Cu, Zn, Mn, Ba, Co, Ni, Na, K, Ca, Sn, Cr, Fe, Li, TI, Mg, Sr, Ga, Sb, V, Hf, Th, Ce, Ge, U, Nb, Ta, and W, R is an alkyl or acyl group, and x is an integer having a value of from 1 to 5. The modifying component is thereby introduced onto and/or into the catalyst support to form a protected modified catalyst support which is less soluble in the aqueous acid and/or the neutral aqueous solution. No calcination of the protected modified catalyst support is effected.

Abstract: A process for producing liquid and, optionally, gaseous products from gaseous reactants includes feeding, at a low level, gaseous reactants into a slurry bed, allowing the gaseous reactants to react as they pass upwardly through the slurry bed, withdrawing any gaseous product and unreacted gaseous reactants from a head space above the slurry bed and withdrawing liquid product and/or slurry bed to maintain the slurry bed at a desired level. The process further includes passing boiler water, as a first heat transfer fluid, in indirect heat exchange relationship through the slurry bed to remove heat from the slurry bed, allowing the heated boiler water to flash and separate to form pressurised steam, controlling the pressure of the steam to be substantially constant, and passing a second heat transfer fluid in indirect heat exchange relationship through the slurry bed to remove heat from the slurry bed.

Abstract: A cobalt catalyst precursor includes a catalyst support impregnated with cobalt. All reducible cobalt is present in the support as supported cobalt oxide of formula-unit CoOaHb, where a≧1,7 and b≧0. A process for preparing a cobalt catalyst precursor, and a process for preparing a cobalt catalyst are also provided.

Abstract: A process for producing liquid hydrocarbon products includes converting a natural gas feedstock to synthesis gas, which is reacted, in a hydrocarbon synthesis stage and by a Fischer-Tropsch reaction, to produce a range of hydrocarbon product. An overheads vapour phase is separated from a liquid phase, and fed to a product condensation stage, where condensation of some components thereof takes place. A vapour phase, an aqueous phase, and a condensed product phase are withdrawn. The vapour phase is fed to a vapour phase work-up stage where a gas component comprising increased concentrations of CO and H2, relative to the vapour phase feed to the vapour phase work-up stage, is recovered, with this gas component being recycled to the hydrocarbon synthesis stage.

Abstract: A process for producing oxygenated products from an olefin-rich feedstock comprise reacting, in a hydroformylation stage, a Fischer-Tropsch derived olefinic product comprising linear and methyl branched olefins, with carbon monoxide and hydrogen in the presence of a catalytically effective quantity of a hydroformylation catalyst and under hydroformylation reaction conditions, to produce oxygenated products comprising linear and methyl branched aldehydes and/or alcohols. The Fischer-Tropsch derived olefinic product is that obtained by subjecting a synthesis gas comprising carbon monoxide (CO) and hydrogen (H2) to Fischer-Tropsch reaction conditions in the presence of a Fischer-Tropsch catalyst.

Abstract: A process for producing oxygenated products from an olefin-rich feedstock comprise reacting, in a hydroformylation stage, a Fischer-Tropsch derived olefinic product comprising linear and methyl branched olefins, with carbon monoxide and hydrogen in the presence of a catalytically effective quantity of a hydroforhylation catalyst and under hydroformylation reaction conditions, to produce oxygenated products comprising linear and methyl branched aldehydes and/or alcohols. The Fischer-Tropsch derived olefinic product is that obtained by subjecting a synthesis gas comprising carbon monoxide (CO) and hydrogen (H2) to Fischer-Tropsch reaction conditions in the presence of a Fischer-Tropsch catalyst.

Abstract: This invention relates to a process for selectively producing linear alcohols, olefins and paraffins from hydrogen-poor carbonaceous fuels such as coal, petroleum coke, or heavy residue oil in a Fischer-Tropsch reactor. The process includes producing synthesis gas, modifying the ratio of hydrogen to carbon monoxide in the synthesis gas to a ratio that is at or above the overall H2/CO usage ratio in the reactor, but less than 2. The modified synthesis gas is combined with a recycled vapor product from the reactor to provide combined synthesis gas having a hydrogen/carbon monoxide ratio of greater than 2 and less than 3. The combined synthesis gas is introduced into the reactor, and the hydrogen and carbon monoxide in the combined synthesis gas is reacted with an iron-based catalyst under Fischer-Tropsch conditions.

Abstract: A process for producing liquid hydrocarbon products includes converting a natural gas feedstock to synthesis gas, which is reacted, in a hydrocarbon synthesis stage and by a Fischer-Tropsch reaction, to produce a range of hydrocarbon products. An overheads vapour phase is separated from a liquid phase, and fed to a product condensation stage, where condensation of some components thereof takes place. A vapour phase, an aqueous phase, and a condensed product phase are withdrawn. The vapour phase is fed to a vapour phase work-up stage where a gas component comprising increased concentrations of CO and H2, relative to the vapour phase feed to the vapour phase work-up stage, is recovered, with this gas component being recycled to the hydrocarbon synthesis stage.

Abstract: A process for producing oxygenated products from an olefinic feedstock, which process includes reacting, in a hydroformylation reaction stage, an olefin feedstock with carbon monoxide and hydrogen at elevated temperature and superatmospheric pressure in the presence of a hydroformylation catalyst. The hydroformylation catalyst comprises a mixture of a metal, M, where M is cobalt (Co), rhodium (Rh), ruthenium (Ru) or palladium (Pd); carbon monoxide; and a bicyclic tertiary phosphine having a ligating phosphorus atom. The ligating phosphorus atom is neither in a bridgehead position nor a member of a bridge linkage. The process produces oxygenated products comprising aldehydes and/or alcohols.

Abstract: An integrated process for producing hydrocarbon products and energy includes reforming a hydrocarbonaceous gaseous feed stock to synthesis gas, and exothermally reacting the synthesis gas at elevated temperature and pressure, and in the presence of a Fischer-Tropsch catalyst, to produce a range of hydrocarbon products of differing carbon chain lengths. The reaction temperature is controlled by indirect heat exchange of a reaction medium, comprising synthesis gas and hydrocarbon products, with water, with the water being converted to steam (‘FT steam’). The process includes burning a combustible gas in a combustion chamber of a gas turbine generator, to form combusted gas, and expanding the combusted gas through an expansion chamber of the gas turbine generator to form hot flue gas. The gas turbine generator generates electrical energy. The FT steam is superheated by means of hot flue gas, thereby producing superheated FT steam.

Abstract: A polymer includes at least propylene as a first monomeric component, 1-pentene as a second monomeric component, and, as a third monomeric component, a third olefin. The third olefin has fewer than 5 carbon atoms, is linear and is not propylene, or has 5 carbon atoms and is branched, or has more than 5 carbon atoms and is linear or branched.

Abstract: A cobalt based Fischer-Tropsch catalyst which including a porous catalyst support and metallic cobalt crystallites within the support. The catalyst has a proportion of its cobalt in reducible form, with this proportion being expressible as &OHgr; mass %, based on the total pre-reduction catalyst mass. The catalyst also has, when freshly reduced, a mono-modal Gaussian metallic cobalt crystallite size distribution, a metallic cobalt surface area, in m2 per gram of catalyst, of from 0.14 &OHgr; to 1.03 &OHgr;, and a catalyst geometry that ensures a stabilized Fischer-Tropsch synthesis effectiveness factor of 0.9 or greater.

Abstract: A method of treating a catalyst support comprises introducing onto and/or into an untreated catalyst support which is partially soluble in an aqueous acid solution and/or a neutral aqueous solution, Si, Zr, Cu, Zn, Mn, Ba, Co, Ni and/or La as a modifying component. The modifying component is capable, when present in and/or on the catalyst support, of suppressing the solubility of the catalyst support in the aqueous acid solution and/or the neutral aqueous solution. A protected modified catalyst support which is less soluble or more inert in the aqueous acid solution and/or the neutral aqueous solution, than the untreated catalyst support, is thus formed. A method of forming a catalyst from the modified catalyst support is also provided.

Abstract: A method of treating an untreated catalyst support includes contacting an untreated catalyst support which is partially soluble in an aqueous acid and/or a neutral aqueous solution with a modifying component precursor of the formula Me(OR)x where Me is a modifying component selected from Si, Zr, Ti, Cu, Zn, Mn, Ba, Co, Ni, Na, K, Ca, Sn, Cr, Fe, Li, TI, Mg, Sr, Ga, Sb, V, Hf, Th, Ce, Ge, U, Nb, Ta, and W, R is an alkyl or acyl group, and x is an integer having a value of from 1 to 5. The modifying component is thereby introduced onto and/or into the catalyst support to form a protected modified catalyst support which is less soluble in the aqueous acid and/or the neutral aqueous solution. No calcination of the protected modified catalyst support is effected.