Abstract: To generate methane from biomass, a biomass pulp is produced from the biomass with a desired dry mass content being set, and the biomass pulp is placed under pressure. The biomass pulp is heated under pressure in order to liquefy the solid organic components of the biomass pulp. The pressurized and heated biomass pulp is heated further to at least the critical temperature of the biomass pulp. Solids precipitated under pressure and increased temperature are separated from the fluid phase. At least a part of the remaining fluid phase is gasified under pressure and increased temperature by means of a reactor to form a methane-rich gas.

Abstract: Methods and apparatus may permit the generation of consistent output synthesis gas from highly variable input feedstock solids carbonaceous materials. A stoichiometric objectivistic chemic environment may be established to stoichiometrically control carbon content in a solid carbonaceous materials gasifier system. Processing of carbonaceous materials may include dominative pyrolytic decomposition and multiple coil carbonaceous reformation. Dynamically adjustable process determinative parameters may be utilized to refine processing, including process utilization of negatively electrostatically enhanced water species, process utilization of flue gas (9), and adjustment of process flow rate characteristics. Recycling may be employed for internal reuse of process materials, including recycled negatively electrostatically enhanced water species, recycled flue gas (9), and recycled contaminants.

Abstract: This invention teaches a process that includes extraction of gas in which the presence of foam results in the carry over in the outlet gas stream of excessive liquids and/or solids, including the steps of injecting the foam laden gas stream tangentially into a cyclonic separator having an axial gas outlet and a liquid outlet, under conditions in which the inlet stream is subjected to at least about 150 G's, the outlet gas being substantially liquids/solids free and the outlet liquid stream being conveyed for disposal or further processing.

Abstract: A hydrogen generation system includes a fuel container, a spent fuel container, a catalyst system and a control system for generating hydrogen in a manner which provides for a compact and efficient construction while producing hydrogen from a reaction involving a hydride solution such as sodium borohydride.

Abstract: The invention describes a system and method for hydrogen sulfide decontamination of natural gas using a scavenging reagent. The system uses a scavenging reagent within two reactors wherein the consumption of scavenging reagent is optimized by the control of flow of clean and partially-consumed scavenging reagent within and between the two reactors.

Abstract: A process for obtaining a heating fluid as indirect heat source for carrying out endothermic reactions, includes the steps of feeding a flow comprising hydrocarbons and a gas flow comprising oxygen to a combustor wherein such flows are suitably compressed. The hydrocarbons are burned in the presence of the oxygen in the combustor thus obtaining the high temperature fluid comprising carbon dioxide and oxygen.

Abstract: Selective, irreversible removal of hydrogen sulfide (H2S) and other sulfhydryl compounds from a gas stream, such as sour natural gas and sour hydrocarbon liquids is achieved with a scavenging agent having hydroxyalkyl functionality and alkylamine functionality. This scavenger possesses a higher capacity for H2S removal compared with a scavenger having only hydroxyalkyl functionality. The scavenging agent is made by reacting at least one alkanolamine and at least one alkyl amine with an aldehyde, such as formaldehyde.

Abstract: A process for the removal of hydrogen sulfide and mercaptans from a gas stream containing a high ratio of mercaptans to hydrogen sulfide, wherein the first step removes hydrogen sulfide by washing the gas stream with an aqueous washing solution comprising water, a physical solvent and a chemical solvent. The first removal step is followed by a second removal step by which mercaptans are removed from the washed gas stream by means of molecular sieves.

Abstract: An improved integrated process for H2S-containing natural gas conversion comprising purification process which generates a H2S-rich gas stream and purified natural gas and an H2S conversion process which generates energy, solid sulfur, and a sulfur-plant tail gas, and an energy-consuming natural gas conversion process selected from the group consisting of liquefaction of the purified natural gas to make LNG, synthesis gas production by partial oxidation of the purified natural gas with oxygen and combinations. The energy consuming step in the liquefaction process is separation of air to give oxygen. At least a portion of the energy release in the H2S conversion process is used to supply at least a portion of the energy needed in the energy-consuming natural gas conversion process. The energy from the H2S conversion process can be in the form of electricity or preferably steam.

Abstract: The present invention provides a method for removing sulfur species from a gas stream without the use of a sulfur species removal process, such as an amine scrub. The sulfur species are removed by directly subjecting the gas stream to a sulfur recovery process, such as a Claus or sub-dewpoint Claus process at high pressure and moderate temperatures, wherein the sulfur recovery process comprises a catalyst which does not comprise activated carbon.

Abstract: The disclosure relates to an absorbent for removing acid gases from fluids. The absorbent contains at least one tertiary amine, an amine which is selected from hydroxyethylpiperazine, bis(hydroxyethylpiperazine) or a mixture of these and piperazine. The absorbent may optionally contain a physical solvent for the acid gases.

Abstract: A fuel cell system includes a fuel cell unit and a gas-generating system containing at least one reforming unit for obtaining a hydrogen-rich reformate from a fuel. It is possible to supply the reformate at least partly to the anode side of the fuel cell unit. The system may include a first reforming reactor for producing a first reformate with a high outlet temperature; a second reforming reactor for producing a second reformate with a second outlet temperature which is below the first outlet temperature; a mixing element for mixing the first reformate with at least one fuel and located between an outlet of the first reforming reactor and an inlet of the second reforming reactor. The second reformate may be supplied to a gas-purification system and the purified reformate supplied to the fuel cell unit.

Abstract: The present invention relates to a method for recovering methane gas by adding a gas mixture containing N2 and CO2 gases to natural gas hydrate and reacting them. The method for recovering methane gas from natural gas hydrate of the present invention comprises the step of replacing CH4 gas in natural gas hydrate with a gas mixture containing N2 and CO2 gases by adding the gas mixture to the natural gas hydrate. The method for recovering methane gas of the invention assures a recovery rate of CH4 gas much higher than prior art method without dissociating natural gas hydrate layer and utilization of flue gas as a gas mixture containing N2 and CO2 gases, which makes possible its practical application for the production of natural gas in terms of economy and environmental protection.

Abstract: A catalytic reactor comprises a plurality of fluid-impermeable plates defining flow channels between them. Tight fitting within each flow channel is a sheet of corrugated material whose surfaces are coated with catalytic material. At each end of the flow channels are headers to supply gas mixtures to the flow channels, the headers communicating with adjacent channels being separate. The reactor enables different gas mixtures to be supplied to adjacent channels, which may be at different pressures, and the corresponding chemical reactions are also different. Where one of the reactions is endothermic while the other reaction is exothermic, heat is transferred through the wall of the tube separating the adjacent channels, from the exothermic reaction to the endothermic reaction.

Abstract: A gasification furnace and a combustion furnace are integrated with each other to form a single fluidized-bed gasification and combustion furnace in which unburned char generated in the gasification furnace is combusted in the combustion furnace, and the thus generated heat of combustion is utilized as a heat source for gasification. The fluidized-bed gasification and combustion furnace (1) comprises a gasification furnace (3) and a combustion furnace (4) which are divided by a first partition wall (2). In the gasification furnace (3), a revolving flow of the fluidized medium is formed by diffusion devices (32, 33) provided on furnace bottoms, and an upward flow of the fluidized medium partly flows in the combustion furnace (4). The combustion furnace (4) is divided into a main partition wall (5).

Abstract: A compact catalytic reactor comprises a stack of plates (72, 74, 75) to define a multiplicity of first and second flow channels arranged alternately in the stack; each flow channel in which a chemical reaction is to take place is defined by straight-through channels across at least one plate, each such straight-through channel containing a removable gas-permeable catalyst structure (80) incorporating a metal substrate. The first flow channels (76) are oriented in a direction that is perpendicular to that of the second flow channels (77), and between successive second flow channels in the stack the reactor defines at least three side-by-side first flow channels (76); and the reactor incorporates flow diversion means (80; 88) such that the first fluid must flow through at least three such first flow channels (76) in succession, in flowing from an inlet to an outlet. The overall flow paths can therefore be approximately co-current or counter-current.

Abstract: A method and apparatus for the treatment of coal to form a product gas such as methane (CH4), and a high purity carbon product. The method includes contacting a coal-containing feedstock with a treatment gas that includes hydrogen. The coal feedstock can advantageously be a low-grade coal that contains high levels of impurities. The methane product gas can be augmented with hydrogen (H2) gas. Reactants and by-products are advantageously recycled within the process system to enhance the economics of the process.

Abstract: A catalytic reactor comprises a plurality of sheets defining flow channels between then. Within each flow channel is a foil of corrugated material whose surfaces are coated with catalytic material. The flow channels extend in transverse dire options, but the foils are shaped to cause the gas in those channels to flow at least partly in counter current to the gas flowing in the other channels. The reactor incorporates header chambers to supply gas mixtures to the flow channels, each header being in the form of a cap attached to the outside of the back and covering a face of the stack. Hence different gas mixtures are supplied to the different channels which may be at different pressures, and the corresponding chemical reactions are also different, and heat is transferred through the sheets separating the adjacent channels. When the catalyst in one set of flow channels becomes spent, it can be replaced by removing a header.

Abstract: A process and apparatus for producing a synthesis gas for use as a gaseous fuel or as feed into a Fischer-Tropsch reactor to produce a liquid fuel in a substantially self-sustaining process. A slurry of particles of carbonaceous material in water, and hydrogen from an internal source, are fed into a hydro-gasification reactor under conditions whereby methane rich producer gases are generated and fed into a steam pyrolytic reformer under conditions whereby synthesis gas comprising hydrogen and carbon monoxide are generated. A portion of the hydrogen generated by the steam pyrolytic reformer is fed through a hydrogen purification filter into the hydro-gasification reactor, the hydrogen therefrom constituting the hydrogen from an internal source. The remaining synthesis gas generated by the steam pyrolytic reformer is either used as fuel for a gaseous fueled engine to produce electricity and/or process heat or is fed into a Fischer-Tropsch or similar reactor under conditions whereby a liquid fuel is produced.

Abstract: A catalytic reactor comprises a plurality of sheets defining flow channels between them. Within each flow channel is a foil of corrugated material whose surfaces are coated with catalytic material. Flow channels for a first gas extend in oblique directions relative to the flow channels for a second gas. The reactor incorporates header chambers to supply gas mixtures to the flow channels, the headers communicating with adjacent channels being separate. The reactor enables different gas mixtures to be supplied to adjacent channels, which may be at different pressures, and the corresponding chemical reactions are also different. Where one of the reactions is endothermic while the other reaction is exothermic, heat is transferred through the sheets separating the endothermic reaction. When the catalyst in one set of flow channels becomes spent, it can be replaced by removing a header.

Abstract: The gaseous feed flowing in through line 1 is contacted in contacting zone ZA with a liquid solvent flowing in through line 2. The solvent comprises between 0.001% and 100% by weight of a liquid olefin. Contacting in zone ZA is carried out in the presence of an acid catalyst. The purified gaseous feed is discharged from zone ZA through line 3. The sulfide-laden solvent is discharged through line 4, then regenerated in unit RE. The regenerated solvent is recycled through lines 7 and 2 to zone ZA.

Abstract: A catalytic reactor comprises a plurality of thin tray-like metal sheets each with a peripheral rim and arranged as a stack to define first gas flow channels between adjacent sheets, alternating with second gas flow channels between adjacent sheets, so as to ensure good thermal contact between gases in the first and the second gas flow channels. Each sheet also defines at least four apertures for flow of gases, and tubes and seal apertures in one sheet to corresponding apertures in the adjacent sheet. The gas flows through the channels may be guided by corrugations, and are preferably in countercurrent in adjacent channels. Appropriate catalysts are coated onto the sheets and in the two gas flow channels.

Abstract: A catalytic reactor comprises a stack of sheets defining flow channels between them. Within each flow channel is a flexible wire structure whose surfaces are coated with catalytic material. Flow channels for a first gas extend along S-shaped curved paths whereas the flow channels for a second gas are straight. The reactor incorporates header chambers to supply gas mixtures to the flow channels, each header chamber being a rectangular cap attached to a face of the stack. The reactor enables different gas mixtures to be supplied to adjacent channels, which nay be at different pressures, and the corresponding chemical reactions are also different. Where one of the reactions is endothermic while the other reaction is exothermic, heat is transferred through the sheets separating the adjacent channels, from the exothermic reaction to the endothermic reaction. When the catalyst in one set of flow channels becomes spent, it can be replaced by removing a header.

Abstract: A process for carrying out secondary reforming reactions for the production of synthesis gas wherein a gas flow comprising oxygen and a gas flow comprising hydrocarbons are fed into a combustion chamber and are reacted upon mixing, thus obtaining a gas flow comprising hydrogen and carbon monoxide fed in turn to a catalytic bed for carrying out a steam reforming reaction, is distinguished in that it comprises the steps of:—feeding the gas flow comprising oxygen in the combustion chamber in the form of a plurality of jets not laid the one upon the other with respect to the direction of the flow comprising hydrocarbons and generated by corresponding parallel streamtubes having equal velocity;—splitting the plurality of jets within the gas flow comprising hydrocarbons in the combustion chamber so as to mix the gas flow comprising oxygen with amounts of gas flow comprising hydrocarbons at local constant ratio.

Abstract: A process for upgrading at least one of a Fischer-Tropsch naphtha and a Fischer-Tropsch distillate to produce at least one of a gasoline component, a distillate fuel or a lube base feedstock component. The process includes reforming a Fischer-Tropsch naphtha to produce hydrogen by-product and a gasoline component with a research octane rating of at least about 80. The process further includes upgrading a Fischer-Tropsch distillate using the hydrogen by-product to produce a distillate fuel and/or a lube base feedstock component.

Abstract: The invention is directed to a method of fueling gas turbines from natural gas reserves with relatively low methane concentrations. The invention permits the use of such reserves to be used to fuel gas turbines to generate electric power. The method of the invention includes providing a natural gas comprising not more than about 40 percent methane on a volume basis and mixing the methane of the natural gas with hydrogen gas to provide a hydrogen enhanced methane/hydrogen gas blend which has sufficient hydrogen to provide flame stability during burning. Thereafter, if required, the hydrogen enhanced methane/hydrogen gas blend is dehydrated to remove a sufficient amount of water to provide a flame stable hydrogen enhanced dehydrated methane/hydrogen gas blend. The hydrogen enhanced natural gas blend is used to fuel gas turbine generators.

Abstract: A method for the production of hydrogen gas. The hydrogen gas is formed by steam reduction using a metal/metal oxide couple to remove oxygen from water. Steam is contacted with a molten metal mixture including a first reactive metal such as iron dissolved in a diluent metal such as tin. The reactive metal oxidizes to a metal oxide, forming a hydrogen gas and the metal oxide can then be reduced back to the metal for further production of hydrogen without substantial movement of the metal or metal oxide to a second reactor.

Abstract: The invention is directed to a method of fueling gas turbines from natural gas reserves with relatively low methane concentrations. The invention permits the use of such reserves to be used to fuel gas turbines to generate electric power. The method of the invention includes providing a natural gas comprising not more than about 40 percent methane on a volume basis and mixing the methane of the natural gas with hydrogen gas to provide a hydrogen enhanced methane/hydrogen gas blend which has sufficient hydrogen to provide flame stability during burning. Thereafter, if required, the hydrogen enhanced methane/hydrogen gas blend is dehydrated to remove a sufficient amount of water to provide a flame stable hydrogen enhanced dehydrated methane/hydrogen gas blend. The hydrogen enhanced natural gas blend is used to fuel gas turbine generators.

Abstract: Method of determining the gas hydrate formation conditions in a well fluid, comprising the following stages: taking a fluid sample, placing this sample in a calorimetry cell, performing on this sample a reference thermogram in a temperature range between T1 and T2, performing on the same sample a second thermogram in the same range and under a pressure Ph of a hydrocarbon gas, T1 being a temperature low enough to obtain the formation of hydrates in the sample at a gas pressure Ph, T2 being high enough to obtain hydrate dissociation, identifying a peak in the second thermogram corresponding to the hydrates dissociation zone and deducting therefrom a hydrates dissociation temperature.

Abstract: Desulphurization of a hydrocarbon feedstock by subjecting a portion of said feedstock to a pre-treatment step of partial oxidation, optionally in the presence of a catalyst, or adiabatic low temperature catalytic steam reforming, thereby forming a gas stream containing hydrogen, and then passing the resultant hydrogen-containing pre-treated gas stream, together with the remainder, of said hydrocarbon feedstock, through a bed of a hydro-desulphurization catalyst and then through a bed of a particulated absorbent capable of absorbing hydrogen sulphide.

Abstract: Oxygen is removed from natural gas by contacting oxygen-containing natural gas with nitric oxide under conditions sufficient to produce nitrogen dioxide.

Abstract: A process for removing mercury from a gaseous process stream. The process involves contacting a mercury-containing gaseous process stream with a regenerable mercury scavenger solution to form a treated stream having a reduced mercury content as compared to the mercury-containing gaseous process stream and a used scavenger solution having an increased mercury content. The regenerable mercury scavenger solution contains an oxidizing agent such as nitric acid, a complexing agent such as oxygen-containing agents and/or thiol and a solvent, for example, a mixture of methanol and water.

Abstract: The invention disclosed relates to a process for removing hydrogen sulfide from a gas stream, such as sour natural gas, with the formation of elemental sulfur as a by-product. By controlling the reaction conditions, the conversion of hydrogen sulfide is maximized, and the sulfur dioxide selectivity is controlled. Specifically, the sulfuric acid concentration and the reaction temperature may be balanced, depending on the desired product mix.

Abstract: A system and method of generating methane gas from organic material, e.g., animal waste. A mixture known to produce methane gas which may include animal waste and vegetation as desired, is treated, also as desired, with an inoculant and inserted into a plastic bag. The plastic bag is extended at one end beyond the portion filled with organic material to produce a collection space for collecting the gas. As the gas is generated, the gas migrates to the provided space and is released for collection and use as an energy source. An upper passage provided in the material enhances migration of the gas to the provided space. As desired, aeration conduits are provided in the material and upon depletion of the methane gas, the mixture may be treated for composting and used as fertilizer.

Abstract: A process is provided for the in-situ removal of carbon dioxide out of natural gas by diverting a stream of the natural gas to a hydrocarbon reformation unit, which converts this diverted stream of the natural gas into a hydrogen-containing gas, and feeding this hydrogen-containing gas and the (undiverted) natural gas into a methanation unit, where the hydrogen reacts with carbon dioxide to form methane, thereby decreasing the amount of carbon dioxide in the natural gas. A second steam of the natural gas may be diverted from the natural gas and combusted, thereby generating heat which may be used for catalyst regeneration and/or for providing any heat necessary for the reactions occurring in the methanation unit or the hydrocarbon reformation unit.

Abstract: The present invention relates to the use of an absorption liquid for purifying a gas by removal of gaseous, acidic impurities. The gas to be purified can be any gas, such as synthesis gas or natural gas, which contains gaseous, acidic impurities such as CO2, H2S, SO2, CS2, HCN, COS or mercaptans. The absorption liquid comprises: A) from 0.01 to 4% by weight of at least one compound of the formula B) from 0.001 to 8.0% by weight of water, and C) at least one polyalkylene glycol alkyl ether of the formula R1—O—(R2—O)x—R3 to 100% by weight, where R1 is C1-C4-alkyl, R2 is ethylene or 2-methylethylene, R3 is hydrogen or C1-C4-alkyl, R4 is hydrogen or C1-C4-alkyl, R5 is C1-C4-alkylene and X is an integer from 1 to 10. The amine may be N-methyldiethanolamine and the ether may be polyethylene glycol dimethyl ether.

Abstract: A method is provided for reducing the amount of hydrogen sulfide and organic sulfides present in streams, such as natural gas streams, by scrubbing the stream with a composition containing (i) an aqueous phase containing a reaction product resulting from the reaction between an aldehyde, such as formaldehyde, and a first amine, such as monoethanolamine or aminoethylpiperazine, and (ii) an organic phase containing at least a second amine, such as butylamine, pentylamine or hexylamine, to produce: (1) a stream having a diminished amount of sulfide contaminants and (2) a sulfided reaction product, such as trithiane. The sulfided reaction product is solubilized into the organic phase (which precludes the formation of solids), and this resulting sulfided reaction product-containing organic phase is separated from the aqueous phase. The sulfided reaction product-containing organic phase may be used as a corrosion inhibitor, and the composition has reduced foaming characteristics during the scrubbing step.

Abstract: A process is provided for removing sulfur compounds, such as hydrogen sulfide, sulfur oxides and thiols, out of fluids, such as natural gas or natural gas liquids, by contacting the fluid with a physical mixture of iron oxide, zinc oxide or mixtures thereof and an activator, such as platinum oxide, gold oxide, silver oxide, copper oxide, copper metal, copper carbonate, copper alloy, cadmium oxide, nickel oxide, palladium oxide, lead oxide, mercury oxide, tin oxide and cobalt oxide, preferably copper oxide wherein the activator is present in an amount equal to 0.125% by wt. to 5% by wt. of the total physical mixture. The contacting is conducted at a temperature of 300° C. or less.

Abstract: Synthesis gas is produced from a methane-containing reactant gas in a mixed conducting membrane reactor in which the reactor is operated to maintain the product gas outlet temperature above the reactant gas feed temperature wherein the total gas pressure on the oxidant side of the membrane is less than the total gas pressure on the reactant side of the membrane. Preferably, the reactant gas feed temperature is below a maximum threshold temperature of about 1400° F. (760° C.), and typically is between about 950° F. (510° C.) and about 1400° F. (760° C.). The maximum temperature on the reactant side of the membrane reactor is greater than about 1500° F. (815° C.).

Abstract: A process and apparatus for producing a synthesis gas for use as a gaseous fuel or as feed into a Fischer-Tropsch reactor to produce a liquid fuel in a substantially self-sustaining process. A slurry of particles of carbonaceous material in water, and hydrogen from an internal source, are fed into a hydro-gasification reactor under conditions whereby methane rich producer gases are generated and fed into a steam pyrolytic reformer under conditions whereby synthesis gas comprising hydrogen and carbon monoxide are generated. A portion of the hydrogen generated by the steam pyrolytic reformer is fed through a hydrogen purification filter into the hydro-gasification reactor, the hydrogen therefrom constituting the hydrogen from an internal source. The remaining synthesis gas generated by the steam pyrolytic reformer is either used as fuel for a gaseous fueled engine to produce electricity and/or process heat or is fed into a Fischer-Tropsch or similar reactor under conditions whereby a liquid fuel is produced.