A process for producing syngas in a first reactor, the process comprising: feeding carbon dioxide, hydrogen and first hydrocarbons into the first reactor; at least partially oxidizing the first hydrocarbons in the first region of the first reactor; producing syngas from the carbon dioxide, hydrogen and the oxidized first hydrocarbons in a second region of the first reactor.

A catalyst, including: a transition metal; and an organic solvent. The transition metal is dispersed in the organic solvent in the form of monodisperse nanoparticles; the transition metal has a grain size of between 1 and 100 nm; and the catalyst has a specific surface area of 5 and 300 m.sup.2/g. The invention also provides a method for preparing a catalyst, including: 1) dissolving an organic salt of a transition metal in an organic solvent including a polyhydric alcohol, to yield a mixture; and 2) heating and stirring the mixture in the presence of air or inert gas, holding the mixture at the temperature of between 150 and 250° C. for between 30 and 240 min, to yield the catalyst.

Certain embodiments are directed to method for making and using an alkali promoted transition metal sulfide Fischer Tropsch catalyst. Certain embodiments are directed to alkali promoted transition metal sulfide Fischer Tropsch catalyst synthesized using steps comprising (i) mixing an ammonium tetrathiomolybdate (ATM) precursor compound with an alkali metal compound and molybdenum disulfide in deionized water to form a reaction mixture, (ii) heating the reaction mixture at a temperature of at least 200, 250, 300, 350, 400C at a pressure of at lease 900, 1000, 1100, 1500, 2000 psi for more than 0.5 1, 1.5, 2.0, 3 or more hours to form a reaction product, (iii) filtering, washing, and drying the reaction product.

Described herein are catalysts relating to liquid synthesis, methods of their preparation, and methods of their use. In an embodiment according to the present disclosure, a method of producing a catalyst for liquid synthesis comprises: providing a silica oxide support; pretreating the silica oxide support to remove air and moisture; impregnating the pretreated silica oxide support with cobalt from a cobalt source using a cobalt impregnation method; and calcinating the impregnated silica oxide support in an oven with a temperature ramping profile, wherein the calcinating comprises feeding air into the oven.

The invention relates to a method for producing iron-containing shaped catalyst bodies by means of 3D printing technology and to iron-containing shaped catalyst bodies that are obtainable by this method and to their use as catalysts in the ammonia synthesis or the Fischer-Tropsch reaction.

Disclosed is an apparatus and method of preparing synthetic fuel using natural gas extracted from a stranded gas field on land or at sea as a raw material through a compact GTL process or a GTL-FPSO process. A parallel-type gas purification unit for controlling a molar ratio of synthetic gas and a concentration of carbon dioxide in the synthetic gas, in which a CO.sub.2 separation device and a bypass unit are disposed in parallel, is provided and, thus, the gas purification unit may prepare the synthetic gas by a steam carbon dioxide reforming (SCR) reaction using natural gas having different CO.sub.2 contents of various stranded gas fields and then supply the synthetic gas having an optimum composition suitable for a Fischer-Tropsch synthesis.

The invention relates to use of a catalyst comprising particles of nickel dispersed in a porous silica matrix for catalyzing a methanation reaction. There is also described a method for methanation of a feedstock at least comprising gases carbon monoxide and hydrogen, said method comprising contacting the feedstock with the catalyst.

An apparatus and method for producing hydrocarbons including aromatic hydrocarbons and/or lower olefins including propylene from CO H.sub.2 while inhibiting reduction in catalyst activity and enhancing selectivity. The apparatus produces hydrocarbons including aromatic hydrocarbons having 6-10 carbon atoms and/or lower olefins including propylene, and is provided: a first supply unit which supplies a raw material gas containing CO and H.sub.2; and a hydrocarbon production unit to which the raw material gas is supplied from the first supply unit, and which produces the hydrocarbons from CO and H.sub.2 contained in the raw material gas while heating a catalyst structure at a temperature of 150° C. or more and less than 300° C. or at a temperature of 350° C. or more and less than 550° C., the catalyst structure includes supports having a porous structure and including a zeolite-type compound, and a metal fine particle present in the supports, the supports have channels communicating with outside the supports, and a portion of the channels have an average inner diameter of 0.95 nm or less.

Preparation of a catalyst that comprises an active phase of at least one metal of group VIM that is deposited on an oxide substrate, a) An oxide substrate that comprises alumina, silica, or a silica-alumina is provided; b) The oxide substrate of step a) is impregnated by an aqueous or organic solution that comprises at least one metal salt of group VIM that is selected from among cobalt, nickel, ruthenium, and iron, and then the product that is obtained is dried at a temperature of between 60 and 200° C.;

A treatment under water vapor of the solid that is obtained in step b) is carried out at a temperature of between 110 and 195° C. for a length of time of between 30 minutes and 4 hours, in the presence of an air/vapor mixture that comprises between 2 and 50% by volume of water in vapor form.

The present disclosures and inventions relate to methods of reducing and activating a cobalt catalyst by contacting an at least partially oxidized cobalt catalyst with a reducing gas, such as a first, second, and/or third reducing gas, at a temperature from 220 ° C. to 270 ° C. for at least 8 or 50 hours depending on the reducing gas, thereby reducing and activating the cobalt catalyst.