Method and apparatus for sustainable carbon dioxide sequestration
US-2024424442-A1 · Dec 26, 2024 · US
US9468884B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9468884-B2 |
| Application number | US-201214355853-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 28, 2012 |
| Priority date | Nov 9, 2011 |
| Publication date | Oct 18, 2016 |
| Grant date | Oct 18, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The method for eliminating acidic compounds contained in a gaseous effluent consists of placing into contact, in column C 1 , a gaseous effluent 1 with an absorbent solution 4 comprising an aqueous solution of one or a plurality of dihydroxyalkylamines having one of the formulas (I) and (II).
Opening claim text (preview).
The invention claimed is: 1. A process for removing acidic compounds contained in a gaseous effluent, in which a step of absorption of the acidic compounds is performed by placing the gaseous effluent in contact with an absorbent solution comprising: water at least one nitrogenous compound chosen from di(hydroxyalkyl)monoamines corresponding to one of the formulae (I) and (II) below: formula (I) being in which R1 and R6 are independently chosen from a hydrogen atom and an alkyl radical containing from 1 to 4 carbon atoms, and R2, R3, R4 and R5 are chosen without preference from a hydrogen atom and an alkyl radical containing from 1 to 4 carbon atoms, on conditions that at least two of the radicals chosen from R2, R3, R4 and R5 are independently chosen from alkyl radicals containing from 1 to 4 carbon atoms and that two of the at least two of the radicals chosen from R2, R3, R4, and R5 that are independently chosen from alkyl radicals containing from 1 to 4 carbon atoms are linked to one of the carbon atoms located alpha to the nitrogen atom, formula (II) being in which R7 is an alkyl radical containing between 1 and 4 carbon atoms, R8 and R9 are independently chosen from a hydrogen atom and an alkyl radical containing from 1 to 4 carbon atoms, and R10 and R11 are independently chosen from a hydrogen atom and an alkyl radical containing from 1 to 4 carbon atoms, on condition that at least one of the radicals R10 or R11 is an alkyl radical containing between 1 and 4 carbon atoms. 2. The process as claimed in claim 1 , in which the nitrogenous compound is chosen from the following compounds: N-(2′-hydroxyethyl)-2-amino-2-methyl-1-propanol N-(2′-hydroxypropyl)-2-amino-2-methyl-1-propanol and N-(2′-hydroxybutyl)-2-amino-2-methyl-1-propanol 3. The process as claimed in claim 1 , in which the absorbent solution comprises between 10% and 90% by weight of said nitrogenous compound and between 10% and 90% by weight of water. 4. The process as claimed in claim 1 , in which the absorbent solution also comprises a non-zero amount, less than 20% by weight, of a primary or secondary amine. 5. The process as claimed in claim 4 , in which said primary or secondary amine is chosen from the group consisting of: monoethanolamine, N-butylethanolamine, aminoethylethanolamine, diglycolamine, piperazine, N-(2-hydroxyethyl)piperazine, N-(2-aminoethyl)piperazine, morpholine, 3-(methylamino)propylamine, 1,6-hexanediamine, N,N′-dimethyl-1,6-hexanediamine. 6. The process as claimed in claim 1 , in which the absorbent solution also comprises a physical solvent chosen from methanol and sulfolane. 7. The process as claimed in claim 1 , in which the step of absorption of the acidic compounds is performed at a pressure of between 1 bar and 120 bar and at a temperature of between 20° C. and 100° C. 8. The process as claimed in claim 1 , in which, after the absorption step, a gaseous effluent that is depleted in acidic compounds and an absorbent solution that is charged in acidic compounds are obtained, and at least one step of regeneration of the absorbent solution charged with acidic compounds is performed. 9. The process as claimed in claim 1 , in which the regeneration step is performed at a pressure of between 1 bar and 10 bar and at a temperature of between 100° C. and 180° C. 10. The process as claimed in claim 1 , in which the gaseous effluent is chosen from natural gas, synthesis gases, combustion fumes, refinery gases, acidic gases derived from an amine unit, gases derived from a tail reduction unit of the Claus process, biomass fermentation gases, cement works gases and incinerator fumes. 11. The process as claimed in claim 1 , used for the selective removal of H 2 S relative to CO 2 in a gaseous effluent comprising H 2 S and CO 2 .
Secondary amines · CPC title
Hydrogen sulfide · CPC title
Monoamines · CPC title
with two or more hydroxyl groups · CPC title
Flue gases · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.