A system for chemical vapor densification includes a reaction chamber having an inlet and outlet; a trap; a conduit fluidly coupled between the outlet of the reaction chamber and the trap; a cryogenic cooler fluidly coupled to the trap though a frustoconical conduit; a first exit path from the cryogenic cooler that vents hydrogen gas to an exhaust; and a second exit path from the cryogenic cooler that recirculates silane and hydrocarbon-rich gas back to the inlet of the reaction chamberand a related method places a substrate in the reaction chamber; establishes a sub-atmospheric pressure inert gas atmosphere within the reaction chamber; densifies the substrate by inputting virgin gas into the reaction chamber; withdraws effluent gas from the reaction chamber; extracts silane and hydrocarbon-rich gas from the effluent gas; and recirculates the silane and hydrocarbon-rich gas back to the reaction chamber.

The present disclosure relates to a method for separating a carbon isotope and a method for concentrating a carbon isotope using the same, the method for separating a carbon isotope including: cooling a formaldehyde gas to a temperature of from 190K to 250K; and obtaining a mixed gas and residual formaldehyde by photodissociating the cooled formaldehyde gas, the mixed gas including carbon dioxide containing a carbon isotope and hydrogen.

A method for improving thermal efficiency of steam production in a steam reforming based syngas plant is provided. In one embodiment, the method can include the steps of: preheating a hydrocarbon feed stream in a first heat exchanger from a first temperature to a second temperature; preheating the hydrocarbon feed stream in a second heat exchanger to a third temperature, wherein the third temperature is greater than the second temperature; introducing the hydrocarbon feed stream in the presence of steam to a steam methane reformer under conditions effective for producing a product stream comprising hydrogen, carbon oxides, and water vapor; and exchanging heat between the product stream and a boiler feed water stream in a third heat exchanger, wherein prior to exchanging heat with the product stream, the boiler feed water stream is used to provide the preheating to the hydrocarbon feed stream in the first heat exchanger.

A system for chemical vapor densification includes a reaction chamber having an inlet and outlet; a trap; a conduit fluidly coupled between the outlet of the reaction chamber and the trap; a cryogenic cooler fluidly coupled to the trap though a frustoconical conduit; a first exit path from the cryogenic cooler that vents hydrogen gas to an exhaust; and a second exit path from the cryogenic cooler that recirculates silane and hydrocarbon-rich gas back to the inlet of the reaction chamberand a related method places a substrate in the reaction chamber; establishes a sub-atmospheric pressure inert gas atmosphere within the reaction chamber; densifies the substrate by inputting virgin gas into the reaction chamber; withdraws effluent gas from the reaction chamber; extracts silane and hydrocarbon-rich gas from the effluent gas; and recirculates the silane and hydrocarbon-rich gas back to the reaction chamber.

A zero-emission, closed-loop and hybrid solar-produced syngas power cycle is introduced utilizing an oxygen transport reactor (OTR). The fuel is syngas produced within the cycle. The separated oxygen inside the OTR through the ion transport membrane (ITM) is used in the syngas-oxygen combustion process in the permeate side of the OTR. The combustion products in the permeate side of the OTR are CO.sub.2 and H.sub.2O. The combustion gases are used in a turbine for power production and energy utilization then a condenser is used to separate H.sub.2O from CO.sub.2. CO.sub.2 is compressed to the feed side of the OTR. H.sub.2O is evaporated after separation from CO.sub.2 and fed to the feed side of the OTR.

The invention relates to a gas scrubbing process for purifying crude synthesis gas with methanol as a physical absorption medium, wherein an acid gas comprising at least hydrogen sulfide (H.sub.2S) is produced. The acid gas is produced in a hot regenerator arranged downstream of an absorption apparatus and subsequently separated from gaseous methanol in an acid gas separator by cooling and condensation. The acid gas separator has a condensation region and an absorption region, wherein both regions are separated from one another by a gas-permeable tray. This has the result that impurities such as hydrogen cyanide and/or ammonia outgassing from a first acid gas substream are not reabsorbed in the condensation region of the acid gas separator, thus avoiding an accumulation of impurities in the hot regenerator or other parts of the gas scrubbing plant. The invention further relates to an acid gas separator and to the use of the acid gas separator according to the invention in a process according to the invention.

Method and plant for generation of synthesis gas, comprising the steps of air fractionation to give oxygen, nitrogen and tail gas, gasification of a hydrocarbonaceous fuel to give crude synthesis gas and cleaning of the crude synthesis gas by removal of acid gas by means of cryogenic absorption, wherein the absorbent is cooled by means of a compression coolant circuit and the cooling water used is cooled by evaporative cooling by means of the tail gas obtained in the air fractionation.

A raw syngas coming from HT gasification of organic wastes, once cooled in a proper heat recovery boiler or in a quencher is treated in a scrubbing section where, by adding an acidic solution followed by alkaline solution and by a WESP, particulate and chlorine compounds are removed and the syngas is ready for conversion, after its compression. In the conversion step CO is converted into C02 and H2 by adding steam; H2S is reduced to sulphur in a solid form, C02 is removed via cryogenic unit or an amine unit and pure H2 is produced.

Process and apparatus for producing a H.sub.2-containing product and a CO-containing product with CO-containing product turndown capability. The H.sub.2-containing product is produced in a process train with a shift reactor and pressure swing adsorption unit. The CO-containing product is produced in a process train with a CO.sub.2 removal unit and a cryogenic separation unit. During the CO-containing product turndown mode, a portion or all of the CO-containing product is passed to the shift reactor in the H.sub.2-containing product train to form additional H.sub.2.

Process and apparatus for producing a H.sub.2-containing product and a CO-containing product with CO-containing product turndown capability. The H.sub.2-containing product is produced in a process train with a shift reactor and pressure swing adsorption unit. The CO-containing product is produced in a process train with a CO.sub.2 removal unit and a cryogenic separation unit. During the CO-containing product turndown mode, a portion or all of the CO-containing product is passed to the shift reactor in the H.sub.2-containing product train to form additional H.sub.2.