Patent classifications
C10G2/332
Method for preparing iron-based catalyst and iron-based catalyst prepared by the same
A method for preparing an iron-based catalyst, the method including preparing iron ore particles by grinding iron ore; and impregnating the iron ore particles with a first metal and second metal, wherein the first metal is selected from copper, cobalt, or manganese, or a combination thereof, and the second metal is selected from an alkali metal or alkali earth metal, or a combination thereof.
Method for preparing synthetic fuel from natural gas of stranded gas field and associated gas from oil and gas fields by GTL-FPSO process
The present invention relates to a method for preparing a synthetic fuel on a vessel above a stranded gas field or an oil & gas field by a GTL-FPSO process, more particularly to a method for preparing a synthetic fuel with superior economic feasibility, productivity and efficiency using a compact GTL (gas to liquid) apparatus that can be used for a stranded gas field or an oil & gas field and an FPSO (floating production, storage and offloading) process under a condition optimized for the ratio of carbon dioxide in the stranded gas field or the oil & gas field and an apparatus for the same.
FORMING LIGHT HYDROCARBONS
Form liquid product stream that has a C.sub.13 to C.sub.20 hydrocarbon content of less than 5.0 wt % based upon a total weight of the liquid product stream via a process that includes contacting synthesis gas with a sulfurized Zeolite Socony Mobil-5 catalyst. The sulfurized Zeolite Socony Mobil-5 catalyst can include ZSM-5, cobalt, an alkali metal, sulfur, and a reduction promoter.
Iron-based catalyst and method for preparing the same and use thereof
The present invention relates to a method for preparing liquid or solid hydrocarbons from syngas via the Fischer-Tropsch synthesis in the presence of iron-based catalysts, the iron-based catalysts for the use thereof, and a method for preparing the iron-based catalysts; more specifically, in the Fischer-Tropsch reaction, liquid or solid hydrocarbons may be prepared specifically with superior productivity and selectivity for C.sub.5+ hydrocarbons using the iron-based catalysts comprising iron hydroxide, iron oxide, and iron carbide wherein the number of iron atoms contained in the iron hydroxide is 30% or higher, and the number of iron atoms contained in the iron carbide is 50% or lower, relative to 100% of the number of iron atoms contained in the iron-based catalysts.
GTL process and reactor employing a mobile phase and plasma
An alternative process and device for carrying out Fischer Tropsch (FT) syntheses is proposed, allowing the reactant entities that take part in the FT reaction to be activated and their contributions, whether by quantity or by proportion, to be adjusted. The process consists in making a particulate phase, optionally consisting of catalytic particles, flow through a reactor. While flowing through the reactor, the particulate phase is subjected at regular intervals to the action of a plasma obtained from a gas, such as hydrogen, thus enabling hydrogen activation for hydrogenation of carbon monoxide, or carbon monoxide activation in order to lengthen the carbon chains.
Process for preparing a chlorine comprising catalyst, the prepared catalyst, and its use
The invention concerns a process for preparing a chlorine comprising catalyst by (a) providing a Fischer-Tropsch catalyst comprising titania and at least 5 weight percent cobalt; (b) impregnating the catalyst with a solution comprising chloride ions; and (c) heating the impregnated catalyst at a temperature in the range of between 100 and 500° C. for at least 5 minutes up to 2 days. The prepared catalyst preferably comprises 0.13-3 weight percent of the element chlorine. The invention further relates to the prepared catalyst and its use.
Fischer-Tropsch synthesis catalyst containing nitride support, preparation method therefor and use thereof
Disclosed are a Fischer-Tropsch synthesis catalyst, a preparation method therefor and use thereof in a Fischer-Tropsch synthesis reaction. Wherein the catalyst comprises: an active component, being at least one selected from VIIIB transition metals; an optional auxiliary metal; and a nitride carrier having a high specific surface area. The catalyst is characterized in that the active metal is supported on the nitride carrier having the high specific surface, such that the active component in the catalyst is highly dispersed. The catalyst has a high hydrothermal stability, an excellent mechanical wear resistance, a high Fischer-Tropsch synthesis activity and an excellent high-temperature stability.
REGENERATION OF CATALYST
A catalyst is regenerated by an inventive process using a heat exchange fluid such as superheated steam to remove heat during the process relying on efficient heat transfer (e.g., enabled by the microchannel reactor construction) in comparison with prior art heat exchange relying on a phase change, e.g. between water and (partial or complete vaporization) steam, allows simplification of the protocols to enable transition at higher temperatures between steps which translates in reduced duration of the regeneration process and avoids potential water hammering risks.
FISCHER-TROPSCH CATALYSTS
The invention relates to the preparation of a Fischer-Tropsch catalyst support and of a Fischer-Tropsch catalyst. A silica comprising support is subjected to hydrothermal treatment. The hydrothermal treatment results in catalysts having improved C.sub.5+ selectivity as compared with catalysts prepared with a non-treated silica comprising support.
SUPPORTED CATALYST, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF
A supported catalyst has a support and a metal active component disposed on the support. The metal active component is at least one selected from the group consisting of a Group VIB metal element and a Group VIII metal element. The support contains at least one of heat-resistant inorganic oxides and molecular sieves and includes an internal channel penetrating the support. The ratio of the cross-section area of the channel to the cross-section area of the support is 0.05-3:100. The difference R between the water absorption rate and the BET pore volume of the support is not less than 0.2 mL/g. The supported catalyst can be used as a hydrogenation catalyst. When used in the hydrocracking of hydrocarbon oils, it can achieve high catalytic activity and high yield of jet fuels at the same time. The supported catalyst can also be used as a Fischer-Tropsch synthesis catalyst.