According to one aspect of the present invention, a hydrogen production apparatus includes a hydrogen production mechanism configured to produce a hydrogen gas from a raw material by using a catalyst; and an operation control circuit configured to input a parameter value as an index indicating a state of the catalyst, and configured to control an operation maximum load of the hydrogen production mechanism to be variable in correspondence with the parameter value.

Provided is a method for preparing synthesis gas, and more particularly, a method for preparing synthesis gas including: mixing a pyrolysis fuel oil (PFO) stream including a PFO and a pyrolysis gas oil (PGO) stream including a PGO discharged from a naphtha cracking center (NCC) process to produce a mixed oil stream (S10); and supplying the mixed oil stream to a combustion chamber for a gasification process to obtain synthesis gas (S20), wherein a ratio of a flow rate of the PGO stream in the mixed oil stream to a flow rate of the mixed oil stream is 0.01 to 0.3.

A method of dry reforming of methane (CH.sub.4) is provided. The method includes contacting at a temperature of 500 to 1000 degree Celsius (° C.) a reactant gas mixture including methane and carbon dioxide (CO.sub.2) with a bimetallic supported catalyst. The bimetallic supported catalyst includes a porous catalyst support and a bimetallic catalyst. The porous catalyst support includes aluminum oxide (Al.sub.2O.sub.3) and magnesium oxide (MgO). The bimetallic catalyst includes nickel (Ni) and copper (Cu) disposed on the porous catalyst support. The method further includes collecting a product gas mixture including hydrogen (H.sub.2) and carbon monoxide (CO). The bimetallic supported catalyst includes 8 to 16 weight percent (wt. %) nickel and 2 to 14 wt. % copper, each based on a total weight of bimetallic supported catalyst.

A method of producing hydrogen using biomass includes: pretreating the biomass using an ionic liquid; and extracting hydrogen by reacting the pretreated biomass with an alkaline substance.

The invention relates to a process for the production of hydrogen-enriched synthesis gas by a catalytic water-gas shift reaction, comprising the steps: introducing a gaseous flow (1) comprising at least one organic sulphide, optionally in its oxide form, in a first reactor (2) comprising a catalyst X.sub.1, collecting a sulfur-containing gaseous flow (3) from the first reactor, introducing the raw synthesis gas (4) in a second reactor (6), introducing the sulfur-containing gaseous flow (3) in the second reactor where the catalytic water-gas shift reaction takes place and comprising a sulfur-resistant shift catalyst X.sub.2, collecting an outlet flow (7) comprising hydrogen-enriched synthesis gas from the second reactor.

The invention also relates to the use of said at least one organic sulphide, optionally in its oxide form, in a process for the production of hydrogen-enriched synthesis gas by a catalytic water-gas shift reaction.

A process for the production of syngas, comprising the steps of generating hydrogen and/or carbon monoxide from a hydrocarbon gas by contacting said hydrocarbon gas with a metal oxide in a first non-stoichiometric state MxOy-α such as to reduce said metal oxide in a first non-stoichiometric state MxOy-α towards a second non-stoichiometric state MxOy-β; generating hydrogen and/or carbon monoxide from a regenerating gas by contacting the metal oxide in the second non-stoichiometric state MxOy-β with said regenerating gas such as to oxidize the metal oxide in the second non-stoichiometric state MxOy-β towards the first non-stoichiometric state MxOy-α; characterized in that the β>α and α>0 and β<y.

A catalyst system, which is active in pyrolyzing methane at reaction temperatures above 700° C., comprising a molten salt selected from the group consisting of the halides of alkali metals; the halides of alkaline earth metals; the halides of zinc, copper, manganese, cadmium, tin and iron; and mixtures thereof, the molten salt having dispersed therein one or more catalytically active forms of iron, molybdenum, manganese, nickel, cobalt, zinc, titanium, and copper in the form of finely divided elemental metals, metal oxides, metal carbides or mixtures thereof.

A method for producing aqueous hydrochloric acid from flue gases is provided. The method comprises conveying water to a first scrubber (102, 202, 302, 402, 502, 602, 702) or to a line (112b, 212b, 312b, 412b, 512b, 712b, 712c) to use the water in a scrubbing liquid of the first scrubber. The method also comprises providing flue gas containing chlorides into the first scrubber (102, 202, 302, 402, 502, 602, 702) and scrubbing the flue gas containing chlorides with the scrubbing liquid by contacting the flue gas with the scrubbing liquid in the first scrubber (102, 202, 302, 402, 502, 602, 702). Dilute hydrochloric acid and a flue gas derivate (104, 204, 304, 404, 504, 704) are produced. The method comprises letting out at least some of the dilute hydrochloric acid from the first scrubber (102, 202, 302, 402, 502, 602, 702) as a scrubber bleed, separating solids suspended by the scrubber bleed in a solids separator (192, 592, 692), conveying the scrubber bleed from the solids separator (192, 592, 692) into an evaporation vessel (194, 594, 694) and concentrating the scrubber bleed in the evaporation vessel (194, 594, 694) to produce hydrochloric acid vapor having a concentration of 5-22 wt-%. A corresponding system is also provided.

A method and apparatus for decarbonizing gases using pressure swing in a first and second pressure vessel that each comprise a fixed bed sorbent. Syngas and steam are received in the first pressure vessel. A carbonation reaction is performed in the first pressure vessel that reacts carbonaceous species in the received syngas with the received steam to produce carbon dioxide and hydrogen. Decarbonated syngas is exhausted from first pressure vessel. A calcination reaction is performed in the second pressure vessel to produce carbon dioxide. A vacuum is provided to the second pressure vessel that causes carbon dioxide to exhaust from the second pressurized vessel at a pressure that substantially follows the decomposition pressure line.

A process is described for steam reforming a hydrocarbon feedstock containing one or more nitrogen compounds, comprising passing a mixture of the hydrocarbon feedstock and steam through a catalyst bed consisting of one nickel steam reforming catalysts disposed within a plurality of externally heated tubes in a tubular steam reformer, wherein each tube has an inlet to which the mixture of hydrocarbon and steam is fed, an outlet from which a reformed gas containing hydrogen, carbon monoxide, carbon dioxide, steam, ammonia and methane is recovered, and the steam reforming catalyst at least at the outlet of the tubes is a particulate eggshell steam reforming catalyst comprising 2.5 to 9.5% by weight nickel, expressed as NiO, wherein the nickel is provided in a layer at the surface of the catalyst and the thickness of layer is in the range of 100 to 1000 μm.