Abstract: Disclosed is a process for converting synthesis gas to liquid hydrocarbon mixtures useful in the production of fuels and petrochemicals. The synthesis gas is contacted with at least two layers of synthesis gas conversion catalyst wherein each synthesis gas conversion catalyst layer is followed by a layer of hydrocracking catalyst and hydroisomerization catalyst or separate layers of hydrocracking and hydroisomerization catalysts. The process can occur within a single reactor, at an essentially common reactor temperature and an essentially common reactor pressure. The process provides a high yield of naphtha range liquid hydrocarbons and a low yield of wax.

Abstract: A unique process and catalyst is described that operates efficiently at low pressures for the direct production of a high cetane diesel type fuel or diesel type blending stock from stoichiometric mixtures of hydrogen and carbon monoxide. This invention allows for, but is not limited to, the economical and efficient production high quality diesel type fuels from small or distributed fuel production plants that have an annual production capacity of less than 100 million gallons per year by eliminating traditional hydrocracking and other costly upgrading processes. This catalytic process is ideal for distributed diesel fuel production plants such as biomass to fuel production plants and stranded natural gas to diesel fuel production plants, and other applications that require optimized economics based on supporting distributed feedstock resources.

Abstract: The invention relates to a catalytically active body for the synthesis of dimethyl ether from synthesis gas. In particular, the invention relates to an improved catalytically active body for the synthesis of dimethyl ether, whereby the components of the active body comprise a defined particle size distribution. Furthermore, the present invention concerns a method for the preparation of a catalytically active body, the use of the catalytically active body and a method for preparation of dimethyl ether from synthesis gas.

Abstract: The invention relates to a process for preparing olefins from synthesis gas, wherein the synthesis gas is contacted with a catalyst which contains cobalt, manganese and a third element selected from the group consisting of aluminium, gallium, indium, thallium, tin, lead and bismuth. Further, the invention relates to a process for preparing such catalyst, and to the catalyst so obtained.

Abstract: A process and system for producing high octane fuel from carbon dioxide and water is disclosed. The feedstock for the production line is industrial carbon dioxide and water, which may be of lower quality. The end product can be high octane gasoline, high cetane diesel or other liquid hydrocarbon mixtures suitable for driving conventional combustion engines or hydrocarbons suitable for further industrial processing or commercial use. Products, such as dimethyl ether or methanol may also be withdrawn from the production line. The process is nearly emission free and reprocesses all hydrocarbons not suitable for liquid fuel to form high octane products. The heat generated by exothermic reactions in the process is fully utilized as is the heat produced in the reprocessing of hydrocarbons not suitable for liquid fuel.

Abstract: The invention is directed to a process to prepare metal nanoparticles or metal oxide nanoparticles by applying a cathodic potential as an alternating current (ac) voltage to a solid starting metal object which solid metal object is in contact with a liquid electrolyte comprising a stabilising cation. The invention is also directed to the use of the nanoparticles as a catalyst.

Abstract: A method is provided for converting synthesis gas to liquid hydrocarbon mixtures useful as distillate fuel and/or lube base oil containing no greater than about 25 wt % olefins and containing no greater than about 5 wt % C21+ normal paraffins. The synthesis gas is contacted with a synthesis gas conversion catalyst comprising a Fischer-Tropsch synthesis component and an acidic component in an upstream catalyst bed thereby producing a wax-free liquid containing a paraffin component and an olefin component. The olefin component is saturated by contacting the liquid with an olefin saturation catalyst in a downstream catalyst bed.

Abstract: The present invention includes a removable microchannel unit including an inlet orifice and an outlet orifice in fluid communication with a plurality of microchannels distributed throughout the removable microchannel unit, and a pressurized vessel adapted have the removable microchannel unit mounted thereto, the pressurized vessel adapted to contain a pressurized fluid exerting a positive gauge pressure upon at least a portion of the exterior of the removable microchannel unit. The invention also includes a microchannel unit assembly comprising a microchannel unit operation carried out within a pressurized vessel, where pressurized vessel includes a pressurized fluid exerting a positive gauge pressure upon an exterior of the microchannel unit operation, and where the microchannel unit operation includes an outlet orifice in fluid communication with an interior of the pressurized vessel.

Abstract: The present application includes iron catalysts promoted with Mo, K and optionally Cu on a multi-walled carbon nanotube (MWCNT) support for high molecular weight hydrocarbon synthesis from synthesis gas.

Abstract: A Fischer-Tropsch process for converting a syngas to hydrocarbon products in the presence of a permeable composite fibrous catalytic sheet comprised of at least three distinct solid phases. A first solid phase is a 3-dimensional porous network of a non-conductive porous ceramic material. A second solid phase is an electrically conductive phase comprised of randomly oriented electrically conductive fibers. A third phase is comprised of catalytic particles dispersed on said 3-dimensional porous network, said conductive fibers, or both. A fourth phase can be present, which fourth phase is comprised one or more conductive species or one or more non-conductive species embedded in said first solid phase.

Abstract: A carbonaceous feedstock to alcohol conversion process in which carbon dioxide is removed from the syngas stream issuing from a feedstock reformer, to yield a carbon dioxide depleted syngas stream including hydrogen, carbon monoxide and methane. This carbon dioxide depleted syngas stream is then passed through a Fischer-Tropsch reactor ultimately yielding a mixed alcohol product which is preferably largely ethanol. The removed carbon dioxide stream is passed through a methane reformer along with methane, which is produced in or has passed through a Fischer-Tropsch reactor, to yield primarily carbon monoxide and hydrogen. The carbon monoxide and hydrogen stream from the methane reformer are passed through the alcohol reactor. Also disclosed are a unique catalyst, a method for controlling the content of the syngas formed in the feedstock reformer, and a feedstock handling system.

Abstract: A catalyst composition contains an active metal on a support including a high surface area substrate and an interstitial compound, for example molybdenum carbide. Pt—Mo2C/Al2O3 catalysts are described. The catalyst systems and compositions are useful for carrying out reactions generally related to the water gas shift reaction (WGS) and to the Fischer-Tropsch Synthesis (FTS) process.

Abstract: This invention discloses a method for making a dimethylether (DME) product from a synthesis gas (syngas) in the presence of a catalyst in a fluid pluralized bed reactor operating in the gas phase. The reactions generate a significant amount of heat and the heat management is balanced between supplying quench recycle syngas to the pluralized sections along the reactor and also by controlling the preheat temperature of the reactant streams. Gas phase fluidization of the catalyst is controlled so that the pluralized reactive zones are maintained in a backmix configuration.

Abstract: A process for producing dry alcohol (including ethanol) that comprises at least one stage wherein a gaseous feedstock, which includes alcohol and water, is contacted with carbon monoxide in the presence of a water-gas shift catalyst, at a temperature sufficiently high so that carbon monoxide and water are consumed and carbon dioxide and hydrogen are produced, thereby removing a portion of the water. The process may include multiple stages; the dry alcohol produced contains 99.5 wt. % or greater of alcohol and 0.5 wt. % or less of water.

Abstract: A carbonaceous feedstock to alcohol conversion process in which carbon dioxide is removed from the syngas stream issuing from a feedstock reformer, to yield a carbon dioxide depleted syngas stream including hydrogen, carbon monoxide and methane. This carbon dioxide depleted syngas stream is then passed through a Fischer-Tropsch reactor ultimately yielding a mixed alcohol product which is preferably largely ethanol. The removed carbon dioxide stream is passed through a methane reformer along with methane, which is produced in or has passed through a Fischer-Tropsch reactor, to yield primarily carbon monoxide and hydrogen. The carbon monoxide and hydrogen stream from the methane reformer are passed through the alcohol reactor. Also disclosed are a unique catalyst, a method for controlling the content of the syngas formed in the feedstock reformer, and a feedstock handling system.

Abstract: Disclosed is a process for reacting carbon dioxide with hydrogen. In the process a catalyst having carbon dioxide adsorbed thereto is contacted with hydrogen at an elevated temperature. The catalyst can be regenerated by contacting depleted catalyst with a carbon dioxide source, for example a flue gas of a power plant. In a preferred embodiment carbon dioxide is reacted by in situ hydrolysis of water.

Abstract: A carbon oxides conversion process includes reacting a carbon oxide containing process gas containing hydrogen and/or steam and containing at least one of hydrogen and carbon monoxide in the presence of a catalyst including shaped units formed from a reduced and passivated catalyst powder, the powder including copper in the range 10-80% by weight, zinc oxide in the range 20-90% by weight, alumina in the range 5-60% by weight and optionally one or more oxidic promoter compounds selected from compounds of Mg, Cr, Mn, V, Ti, Zr, Ta, Mo, W, Si and rare earths in the range 0.01-10% by weight, wherein said shaped units have a reduced to as-made mean horizontal crush strength ratio of ?0.5:1 and a copper surface area above 60 m2/g Cu.

Abstract: A process for the synthesis of hydrocarbons by the Fisher Tropsch process includes reacting a mixture of carbon monoxide and hydrogen at elevated temperature and pressure in the presence of a catalyst including 15-50% wt cobalt at least partially in elemental form, supported on an oxidic support of aluminium, oxygen and 0.5-10% wt lithium, where the oxidic support includes lithium oxides and >75% wt of the lithium oxides are lithium aluminate spinel, LiAl5O8.

Abstract: A methanol synthesis process includes reacting a process gas containing hydrogen, carbon dioxide and carbon monoxide over a catalyst including shaped units formed from a reduced and passivated catalyst powder the powder including copper in the range 10-80% by weight, zinc oxide in the range 20-90% by weight, alumina in the range 5-60% by weight and optionally one or more oxidic promoter compounds selected from compounds of Mg, Cr, Mn, V, Ti, Zr, Ta, Mo, W, Si and rare earths in the range 0.01-10% by weight, to form a product gas, and condensing methanol, water and oxygenate by-products therefrom, wherein the total oxygenate by-product level in the condensate is below 500 ppm.

Abstract: The present invention relates to petrochemistry and gas chemistry, and discloses a support for catalysis of exothermic processes, particularly the Fischer-Tropsch process, methanol synthesis, hydrogenation and purification of exhaust gases. The support comprises metallic aluminium in the form of a mixture of dispersed powders of flaky and spherical aluminium and the support is in the form of pellets, preferably cylinders, tablets, balls, obtained by extrusion, pelletization, tabletting, rounding or liquid molding. The catalyst prepared on the support comprises an active metal selected from the group consisting of Co, Fe, Ni, Ru, Rh, Pt, Pd, Cu and mixtures thereof.

Abstract: The present invention provides a process for preparing methanol, dimethyl ether, and low carbon olefins from syngas, wherein the process comprises the step of contacting syngas with a catalyst under the conditions for converting the syngas into methanol, dimethyl ether, and low carbon olefins, characterized in that, the catalyst contains an amorphous alloy consisting of a first component Al and a second component, said second component being one or more elements or oxides thereof selected from Group IA, IIIA, IVA, VA, IB, IIB, IVB, VB, VIIB, VIIB, VIII, and Lanthanide series of the Periodic Table of Elements, and said second component being different from the first component Al. According to the present process, the syngas can be converted into methanol, dimethyl ether, and low carbon olefins in a high CO conversion, a high selectivity of the target product, and high carbon availability.

Abstract: The present invention provides a process for preparing methanol, dimethyl ether, and low carbon olefins from syngas, wherein the process comprises the step of contacting syngas with a catalyst under the conditions for converting the syngas into methanol, dimethyl ether, and low carbon olefins, characterized in that, the catalyst contains an amorphous alloy consisting of components M and X wherein the component X represents an element B and/or P, the component M represents two or more elements selected from Group IIIA, IVA, VA, IB, IIB, IVB, VB, VIB, VIIB, VIII and Lanthanide series of the Periodic Table of Elements. According to the present process, the syngas can be converted into methanol, dimethyl ether, and low carbon olefins in a high CO conversion, a high selectivity of the target product, and high carbon availability.

Abstract: This invention relates to a method for the preparation of a hydrocarbon synthesis catalyst material, in the form of a hydrocarbon synthesis catalyst precursor and/or catalyst, preferably, a Fischer Tropsch synthesis catalyst precursor and/or catalyst. The invention also extends to the use of a catalyst precursor and/or catalyst prepared by the method according to the invention in a hydrocarbon synthesis process, preferably, a Fischer Tropsch synthesis process. According to this invention, a method for the preparation of a hydrocarbon synthesis catalyst material includes the steps of treating Fe(II) carboxylate in solution with an oxidising agent to convert it to Fe(III) carboxylate in solution under conditions which ensure that such oxidation does not take place simultaneously with any dissolution of Fe(0); and hydrolysing the Fe(III) carboxylate solution resulting from step (iii) and precipitating one or more Fe(III) hydrolysis products.

Abstract: A process is disclosed for the production of ethanol whereby synthesis gas is reacted to produce ethanol and carbon dioxide in the presence of a compound catalyst at a temperature in the range of 250° C. to 350° C. and a pressure of 1 atm. to 20 atm.

Abstract: A method of adapting an axial flow reaction vessel having opposed ports to an opposed axial flow reaction vessel includes installing a process fluid collection system within the body of the vessel in fluid communication with one or more of the ports; providing the vessel with a bed of particulate catalyst or sorbent containing a layer of inert particulate material around the process fluid collection system; and adapting the feed to the vessel through one or more of the ports such that a process fluid fed to the vessel is passed axially and in the opposite direction through the fixed bed of catalyst or sorbent and is collected by the process fluid collection system disposed centrally within the bed and in fluid communication with one or more of the ports.

Abstract: A method is provided for converting synthesis gas to liquid hydrocarbon mixtures useful as distillate fuel and/or lube base oil containing no greater than about 25 wt % olefins and containing no greater than about 5 wt % C21+ normal paraffins. The synthesis gas is contacted with a synthesis gas conversion catalyst comprising a Fischer-Tropsch synthesis component and an acidic component in an upstream catalyst bed thereby producing a wax-free liquid containing a paraffin component and an olefin component. The olefin component is saturated by contacting the liquid with an olefin saturation catalyst in a downstream catalyst bed.

Abstract: This invention relates to a Fe-based catalyst for Fischer-Tropsch synthesis, preparation method and application thereof. The catalyst contains Fe, oxide(s) of IB group metal Cu and/or Ag as a reducing promoter, IA group metal Li, Na, K or Rb as an electron promoter, VIII group noble metal Ru, Rh, Pd or Pt as a hydrogenation promoter and SiO2 as a structure promoter. The preparation method comprises the following steps: preparing a solution of Fe salt; co-precipitating the solution rapidly with an alkaline compound, then washing and pulping again; and adding a solution of IB group metal salt as a reducing promoter, a IA group metal salt solution and silica sol, or adding a solution of IB group metal salt as a reducing promoter and a silicate of IA group metal; then molding by spray-drying, impregnating in a solution of VIII group noble metal salt, and drying and roasting to obtain the catalyst. The catalyst is suitable for producing hydrocarbons by a low temperature Fischer-Tropsch synthesis process.

Abstract: This invention relates to a hydrocarbon synthesis process. More particularly, but not exclusively, this invention relates to a Fischer Tropsch Process employing an activated catalyst and to the use of such an activated catalyst, wherein the Fischer Tropsch Process conditions favour the attainment of a low acid selectivity. More particularly the invention relates to a three-phase low temperature Fischer Tropsch (LTFT) process wherein a feed of H2 and CO are converted to hydrocarbons and possible oxygenates thereof by contacting the H2 and CO in the presence of an iron-based Fischer Tropsch catalyst in a reaction zone, wherein the molar ratio of H2:CO in the feed is from 0.5 and less than 1.

Abstract: The method for manufacturing an unsaturated hydrocarbon and an oxygen-containing compound according to the present invention comprises: a first step of dispersing a catalyst in poly-?-olefin and reducing the catalyst with carbon monoxide or synthesis gas, wherein the catalyst is prepared by supporting iron on a support containing manganese and having an average pore size of 2 to 100 nm; and a second step of bringing the catalyst after reduction in the first step into contact with synthesis gas under the conditions of a reaction temperature of 100 to 600° C. and a reaction pressure of 0.1 to 10 MPa to obtain a reaction product containing an unsaturated hydrocarbon and an oxygen-containing compound.

Abstract: A process is disclosed for converting synthesis gas to a liquid hydrocarbon mixture useful as distillate fuel and/or lube base oil which is substantially free of solid wax. A synthesis gas feed is contacted with a synthesis gas conversion catalyst in an upstream bed and a hydroisomerization catalyst containing a metal promoter and an acidic component in a downstream bed within a single reactor at essentially common reaction conditions. A Fischer-Tropsch wax is formed over the synthesis gas conversion catalyst and said wax is subsequently hydroisomerized over the hydroisomerization catalyst, thereby resulting in a liquid hydrocarbon mixture having a desirable product distribution.

Abstract: A method of producing an iron catalyst for catalyzing the hydrogenation of carbon monoxide is disclosed. The method comprises using a reduced amount of acid for iron dissolution compared to certain previous methods. The resulting acidic iron mixture is heated without boiling to obtain a nitrate solution having a Fe2+:Fe3+ ratio in the range of about 0.01%: 99.99% to about 100%:0% (wt:wt). Iron phases are precipitated at a lower temperature compared to certain previous methods. The recovered catalyst precursor is dried and sized to form particles having a size distribution between 10 microns and 100 microns. In embodiments, the Fe2+:Fe3+ ratio in the nitric acid solution may be in the range of from about 3%:97% to about 30%:70% (wt:wt) and the calcined catalyst may comprise a maghemite:hematite ratio of about 1%:99% to about 70%:30%.

Abstract: A process for the generation of a synthesis gas comprising: (a) forming a raw synthesis gas, (b) dividing the raw synthesis gas into first and second streams, (c) subjecting the first stream to the water gas shift reaction to form a shifted gas mixture, (d) cooling the second raw synthesis gas stream and shifted gas mixture to below the dew point to form a dry raw synthesis gas mixture, and a dry shifted gas mixture respectively, (e) feeding the dry raw synthesis gas mixture and a dry shifted gas mixture to a gas-washing unit operating by counter-current solvent flow, such that the solvent flowing through said unit contacts first with the dry raw gas mixture and then the dry shifted gas mixture, and (f) collecting from said gas-washing unit a synthesis gas having a stoichiometry ratio, R?(H2—CO2)/(CO+CO2), in the range 1.4 to 3.3.

Abstract: A joint process for preparing alcohol/ether mixtures, alcohol/hydrocarbon mixtures and synthesizing ammonia is disclosed. In particular, a process of converting CO and CO2 present in the feed gas of ammonia synthesis, comprising H2 and N2 as major components, into useful co-products is disclosed. The process is characterized in that the alcohol/ether forming reaction is firstly carried out by using a copper series catalyst, then the alcohol/hydrocarbon forming reaction is carried out by using an iron series catalyst, the individually formed alcohol/ether and alcohol/hydrocarbon products are separated by water cooling and condensing, and discharged into corresponding storage tanks, and the remaining gas, in which the amount of CO and CO2 is less than or equal to 10 ppm, is fed into the ammonia synthesis system.

Abstract: Disclosed are a catalyst for synthesis of methanol from synthesis gas and a method for preparing the same. The catalyst includes a Cu—Zn—Al oxide containing CuO, ZnO and Al2O3 in a predetermined ratio or Cu—Zn—Al—Zr oxide containing CuO, ZnO, Al2O3 and ZrO2 in a predetermined ratio, in combination with a cerium-zirconium oxide obtained by a sol-gel process. As compared to the existing Cu—Zn—Al catalysts for synthesizing methanol, the catalyst disclosed herein inhibits formation of byproducts and improves yield of methanol. Therefore, it is possible to improve methanol purification efficiency and carbon conversion efficiency.

Abstract: Iron- and copper-comprising heterogeneous catalyst and process for producing it, which comprises the following steps: I. thermal decomposition of gaseous iron pentacarbonyl to give carbonyl iron powder having spherical primary particles, II. treatment of carbonyl iron powder obtained in step I with hydrogen, resulting in the metallic spherical primary particles at least partly agglomerating, III. surface oxidation of the iron particles from step II (agglomerates=secondary particles, and also any primary particles still present) to form iron oxide, IV. contacting of the particles from step III with an aqueous solution of a copper compound, V. drying in the presence of oxygen and subsequent calcination in the absence of oxygen, resulting firstly in oxygen-comprising copper compounds on the particles and finally reaction of these with the iron oxide to form a mixed oxide of the formula CuxFe3-xO4, where 0<x?1.

Abstract: Catalytic structures include a catalytic material disposed within a zeolite material. The catalytic material may be capable of catalyzing a formation of methanol from carbon monoxide and/or carbon dioxide, and the zeolite material may be capable of catalyzing a formation of hydrocarbon molecules from methanol. The catalytic material may include copper and zinc oxide. The zeolite material may include a first plurality of pores substantially defined by a crystal structure of the zeolite material and a second plurality of pores dispersed throughout the zeolite material. Systems for synthesizing hydrocarbon molecules also include catalytic structures. Methods for synthesizing hydrocarbon molecules include contacting hydrogen and at least one of carbon monoxide and carbon dioxide with such catalytic structures.

Abstract: The present invention relates to a method of producing methanol from a methane source by oxidizing methane under conditions sufficient to a mixture of methanol and formaldehyde while minimizing the formation of formic acid and carbon dioxide. The oxidation step is followed by treatment step in which formaldehyde is converted into methanol and formic acid which itself can further be converted into methanol via catalytic hydrogenation of intermediately formed methyl formate.

Abstract: The invention provides a process for the removal of COS and H2S from a synthesis gas stream comprising COS and H2S, the process having the steps of: removing H2S from a feed synthesis gas stream with a first solid adsorbent to obtain a first synthesis gas stream, converting COS in the first synthesis gas stream to H2S by contacting the first synthesis gas stream with a COS-hydrolysing catalyst in the presence of water in a hydrolysis zone to obtain a second synthesis gas stream depleted of COS and enriched in H2S; and removing H2S from the second synthesis gas stream by contacting the second synthesis gas stream with a second solid adsorbent in a H2S removal zone to obtain a third synthesis gas stream depleted of H2S and depleted of COS to very low levels.

Abstract: The invention relates to a process for preparing Cu/Zn/Al catalysts. In this process, the metals are used in the form of their formates and are precipitated in a suitable form. Suitable precipitants are, for example, alkali metal carbonates. The invention further relates to a catalyst as can be obtained by the process according to the invention and to its use.

Abstract: The present invention relates to a process for the production of ethanol, and optionally methanol, from synthesis gas. In particular the present invention relates to a process for the production of ethanol from a carbonaceous feedstock; wherein the carbonaceous feedstock is first converted to synthesis gas which is then converted to methanol, which is then converted to ethanoic acid, which is then esterified and which is then hydrogenated to produce ethanol in the same alcohol synthesis unit in which the said synthesis gas is converted to methanol.

Abstract: The present invention relates to processes for forming mixed alcohols containing methanol and ethanol. The mixed alcohol can then be used as a feedstock for an oxygenate-to-olefin reaction system for conversion thereof to ethylene, propylene, and the like. In addition, the olefins produced by the oxygenate-to-olefin reaction can then be used as monomers for a polymerization of olefin-containing polymers and/or oligomers.

Abstract: Disclosed is an Cu/Zn/Al-catalyst containing copper oxide and zinc oxide as catalytically active components and aluminium oxide as thermostabilising component. The catalyst is characterized in that the Cu/Zn atomic ratio is <2.8 and the aluminium oxide component is obtained from an aluminium hydroxide sol.

Abstract: A method of producing an iron catalyst for catalyzing the hydrogenation of carbon monoxide is disclosed. The method comprises using a reduced amount of acid for iron dissolution compared to certain previous methods. The resulting acidic iron mixture is heated without boiling to obtain a nitrate solution having a Fe2+:Fe3+ ratio in the range of about 0.01%:99.99% to about 100%:0% (wt:wt). Iron phases are precipitated at a lower temperature compared to certain previous methods. The recovered catalyst precursor is dried and sized to form particles having a size distribution between 10 microns and 100 microns. In embodiments, the Fe2+:Fe3+ ratio in the nitric acid solution may be in the range of from about 3%:97% to about 30%:70% (wt:wt) and the calcined catalyst may comprise a maghemite:hematite ratio of about 1%:99% to about 70%:30%.

Abstract: The present invention relates to a method of producing methanol from a methane source by oxidizing methane under conditions sufficient to a mixture of methanol and formaldehyde while minimizing the formation of formic acid and carbon dioxide. The oxidation step is followed by treatment step in which formaldehyde is converted into methanol and formic acid which itself can further be converted into methanol via catalytic hydrogenation of intermediately formed methyl formate.

Abstract: The invention relates to a method for carrying out heterogeneous catalytic exothermic gas phase reactions at a high temperature and high pressure, during which the synthesis gas comprised of a mixture of make-up gas and/or of recycle gas is fed through at least two synthesis stages that are connected in-series to form a synthesis system. The product gases from the synthesis stages, with the exception of the last stage, are separated into at least two partial flows. One partial flow is cooled until the product is condensated out, and the condensate containing the product is separated from the gaseous constituents. Afterwards, the gaseous constituents are combined with the warm portion of the product gas in order to reach the inlet temperature of the next synthesis stage. In addition, the partial flow from which the product was condensated out and removed, can be heated before being remixed with the warm portion of the product gas.

Abstract: The invention relates to a process for removing carbon monoxide from a hydrogenous gas stream by reacting the carbon monoxide with hydrogen to give methane and water in the presence of a heterogeneous catalyst. In this process, the catalyst is present in the form of a thin-layer catalyst on a support material. The invention further relates to an apparatus for carrying out the process.

Abstract: A method and apparatus for converting organic waste feed streams into usable liquid fuels by adjusting the ratio of carbon dioxide, carbon monoxide, and hydrogen in the effluent gas of a high temperature waste treatment system. A pressure swing adsorption (PSA) unit is used to remove carbon dioxide from the effluent gas of a high temperature waste treatment system, while leaving carbon monoxide and hydrogen, thereby producing a gas stream amenable to the production of methanol and other liquid fuels using commercially available catalytic reactors.

Abstract: The present invention relates to a process for converting synthesis gas to hydrocarbons, in particular to hydrocarbons in the C5-C60 range particularly suitable for use as liquid motor fuels, in a slurry reactor in the presence of a Fischer-Tropsch catalyst comprising cobalt and zinc oxide wherein the Fischer-Tropsch catalyst is activated with a reducing gas consisting of hydrogen and an inert gas at 330 to 400° C. prior to contact with synthesis gas in the slurry reactor.

Abstract: This invention is directed to a process for making a methanol product from a synthesis gas (syngas) feed using a fast fluid bed reactor. The reactor is operated at substantially plug flow type behavior. The heat from circulated catalyst is sufficient to initiate the reaction process with little to no preheating of feed required. In addition, little if any internal reactor cooling is needed.

Abstract: This invention is directed to a process for making a methanol product from a synthesis gas (syngas) feed using a fluid bed reactor. Internal reactor heat transfer is balanced between feed preheat and catalyst bed temperature using appropriate backmixing of feed and catalyst. Backmixing can be appropriately controlled using a number of control points, including any one or more of superficial gas velocity, catalyst density in the reactor, reactor height to diameter ratio (preferably at least in the region of the dense catalyst bed), and catalyst particle size.