The process of the present invention provides high recovery and low capital cost giving it an economic advantage over previously known purification processes. The present process has particular applicability to the purification of synthesis gases comprising at least hydrogen (H.sub.2), carbon monoxide (CO), methane (CH.sub.4), CO.sub.2, and H.sub.2O to obtain a gas stream including at least H.sub.2, CO, and CH.sub.4, that is substantially free of H.sub.2O and CO.sub.2. The process also has applicability to the purification of natural gases inclusive of at least CH.sub.4, N.sub.2, CO.sub.2, and H.sub.2O to produce a gas stream including at least CH.sub.4 and N.sub.2, but which is substantially free of H.sub.2O and CO.sub.2.

A carbon dioxide conversion system for an environment includes a first gas-liquid contactor-separator downstream of the environment; an electrochemical conversion cell downstream of the first gas-liquid contactor-separator; and a cleaned ionic liquid storage intermediate the first gas-liquid contactor-separator and the electrochemical conversion cell.

A carbon dioxide conversion system for an environment includes a first gas-liquid contactor-separator downstream of the environment; an electrochemical conversion cell downstream of the first gas-liquid contactor-separator; and a cleaned ionic liquid storage intermediate the first gas-liquid contactor-separator and the electrochemical conversion cell.

A process can treat a gaseous material mixture obtained by catalytic conversion of synthesis gas that contains at least alkenes, possibly alcohols and possibly alkanes, and also possibly nitrogen as inert gas and unconverted components of the synthesis gas, comprising hydrogen, carbon monoxide and/or carbon dioxide. After catalytic conversion of synthesis gas, separation of the product mixture obtained in this reaction into a gas phase and a liquid phase is performed by at least partial absorption of the alkenes, possibly of the alcohols and possibly of the alkanes, in a high boiling point hydrocarbon or hydrocarbon mixture as an absorption medium, separation as the gas phase of the gases not absorbed into the absorption medium, separating an aqueous phase from the organic phase of the absorption medium, preferably by decanting, and desorption of the alkenes, possibly of the alcohols and possibly of the alkanes, from the absorption medium.

A process can produce alcohols having at least two carbon atoms by catalytic conversion of synthesis gas into a mixture containing alkanes, alkenes, and alcohols. Alkenes are converted into corresponding alcohols in a subsequent step by hydration of the alkanes. Before the hydration and after the catalytic conversion, gas and liquid phases may be separated. Specific catalysts can be employed that have a markedly higher selectivity for alkenes than for alkanes. These catalysts comprise grains of non-graphitic carbon having cobalt nanoparticles dispersed therein. The cobalt nanoparticles have an average diameter d.sub.p from 1 to 20 nm, and an average distance D between nanoparticles is from 2 to 150 nm. The combined total mass fraction of metal ω in the grains ranges from 30% to 70% by weight of the total mass of the grains of non-graphitic carbon, wherein 4.5 dp/ω>D≥0.25 dp/ω.

The invention concerns a plant and a method for treating gas by chemical, physical or hybrid absorption of compounds for removal, comprising at least: a) a step of absorption by contacting a gas for treatment with a depleted solvent to give a treated gas and a rich solvent; b) a step of optional separation by medium-pressure flashing c) a step of heat exchange between a fraction of the cold rich solvent and the hot depleted solvent in a first heat exchanger d) a step of heat exchange between the complementary fraction of the cold rich solvent and a hot gaseous effluent in a second exchanger e) a step of optional separation by low-pressure flashing f) a step of regeneration of the rich solvent by heating in a reboiler g) a step of separation by low-pressure flashing h) a cooling of the depleted solvent.

A gas purification device removes a part of ammonia contained in a first gas; recovers a first off-gas containing the removed ammonia, removes hydrogen sulfide and ammonia from a second gas produced by removing the part of ammonia, recovers a second off-gas containing the removed hydrogen sulfide and ammonia, and combusts the first off-gas and the second off-gas. The gas purification device includes: a first combustion chamber in which combustion is performed in a reducing atmosphere; a second combustion chamber in which combustion is performed in a reducing atmosphere downstream of the first combustion chamber; and a third combustion chamber in which combustion is performed in an oxidizing atmosphere downstream of the second combustion chamber. The first off-gas flows into the first combustion chamber and the second off-gas flows into the third combustion chamber.

A process for sweetening a syngas stream, the process comprising the steps of: providing a syngas stream to a nonselective amine absorption unit, the sour syngas stream comprising syngas, carbon dioxide, and hydrogen sulfide; separating the syngas stream in the nonselective amine absorption unit to obtain an overhead syngas stream and an acid gas stream; introducing the acid gas stream to a membrane separation unit, the acid gas stream comprising hydrogen sulfide and carbon dioxide; separating the acid gas stream in the membrane separation unit to produce a retentate stream and a permeate stream, wherein the retentate stream comprises hydrogen sulfide, wherein the permeate stream comprises carbon dioxide; introducing the retentate stream to a sulfur recovery unit; processing the retentate stream in the sulfur recovery unit to produce a sulfur stream and a tail gas stream, wherein the sulfur stream comprises liquid sulfur.

The invention relates to a process for removal of metal carbonyls from crude synthesis gas in a gas scrubbing process with a physical scrubbing medium. Scrubbing medium laden with hydrogen sulfide (H.sub.2S) and metal carbonyls is sent to a treatment vessel having a residence time region and a scrubbing region. Metal carbonyls are precipitated from the laden scrubbing medium as metal sulfides in the residence time region. The scrubbing region is supplied with a regenerated scrubbing medium. According to the invention it is provided that the residence time region and the scrubbing region are separated from one another by a gas-permeable tray, a regenerated scrubbing medium-comprising liquid layer adjacent to the gas-permeable tray is formed in the scrubbing region, metal carbonyls outgassing from the residence time region pass through the gas-permeable tray and are absorbed by regenerated scrubbing medium in the scrubbing region, wherein scrubbing medium comprising metal carbonyls is obtained and metal carbonyls outgassing from the residence time region are cooled by the liquid layer. The invention further relates to a treatment vessel, to the use of the process, treatment vessel or apparatus according to the invention in a gas scrubbing process with methanol as the physical scrubbing medium and to the use of the treatment vessel in a process according to the invention.

An aminated magnesium oxide adsorbent containing a magnesium oxide matrix having disordered mesopores and a BET surface area of 320 to 380 m.sup.2/g, and a polyamine selected from the group consisting of an ethyleneamine having a molecular weight of up to 450 g/mol and a polyethylene imine having a number average molecular weight of greater than 500 g/mol and up to 20,000 g/mol, wherein the polyamine is impregnated within the disordered mesopores of the magnesium oxide matrix. A method of making the aminated magnesium oxide adsorbent and a method of capturing CO.sub.2 from a gas mixture with the aminated magnesium oxide adsorbent are also described.