Method and apparatus for sustainable carbon dioxide sequestration
US-2024424442-A1 · Dec 26, 2024 · US
US9724642B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9724642-B2 |
| Application number | US-201414555787-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 28, 2014 |
| Priority date | Dec 3, 2013 |
| Publication date | Aug 8, 2017 |
| Grant date | Aug 8, 2017 |
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.
An acid gas absorbent includes at least one kind of secondary amine compound represented by formula (1): where R 1 is a cyclopentyl group or a cyclohexyl group which may be substituted by a substituted or non-substituted alkyl group having 1 to 3 carbon atoms, R 2 and R 3 each indicate an alkylene group having 2 to 4 carbon atoms, and R 2 and R 3 may each be the same or different, and be a straight chain or have a side chain.
Opening claim text (preview).
What is claimed is: 1. An acid gas absorbent comprising 45 mass % to 55 mass % of at least one secondary amine compound represented by general formula (1), where R 1 indicates a cyclopentyl group which may be substituted by a substituted or non-substituted alkyl group having 1 to 3 carbon atoms, R 2 and R 3 , which may be the same or different, each indicate an alkylene group having 2 to 4 carbon atoms and are a straight chain or have a side chain. 2. The acid gas absorbent according to claim 1 , wherein, in the secondary amine compound represented by the general formula (1), R 2 and R 3 each independently indicate an alkylene group having 2 or 3 carbon atoms. 3. The acid gas absorbent according to claim 1 , further comprising water. 4. The acid gas absorbent according to claim 1 , comprising water and 45 mass % to 55 mass % of 2-[2-(cyclopentylamino)ethoxy]ethanol. 5. The acid gas absorbent according to claim 1 , comprising water and 45 mass % to 55 mass % of 3-[2-(cyclopentylamino)ethoxy]-1-propanol. 6. The acid gas absorbent according to claim 1 , comprising water and 45 mass % to 55 mass % of 4-[2-(cyclopentylamino)ethoxy]-1-butanol. 7. The acid gas absorbent according to claim 1 , wherein the at least one secondary amine compound represented by general formula (1) is selected from 2-[2-(cyclopentylamino)ethoxy]ethanol, 2-[3-(cyclopentylamino)propoxy]ethanol, 2-[4-(cyclopentylamino)butoxy]ethanol, 3-[2-(cyclopentylamino)ethoxy]-1-propanol, 3-[3-(cyclopentylamino)propoxy]-1-propanol, 3-[4-(cyclopentylamino)butoxy]-1-propanol, 1-[2-(cyclopentylamino)ethoxy]-2-propanol, 1-[3-(cyclopentylamino)propoxy]-2-propanol, 1-[4-(cyclopentylamino)butoxy]-2-propanol, 4-[2-(cyclopentylamino)ethoxy]-1-butanol, 4-[3-(cyclopentylamino)propoxy]-1-butanol, and 4-[4-(cyclopentylamino)butoxy]-1-butanol. 8. The acid gas absorbent according to claim 1 , further comprising 1 mass % to 20 mass % of an alkanolamine and/or a heterocyclic amine compound 9. The acid gas absorbent according to claim 8 , comprising an alkanolamine which is at least one selected from the group consisting of 2-(isopropylamino)ethanol, 2-(ethylamino)ethanol, and 2-amino-2-methyl-1-propanol. 10. The acid gas absorbent according to claim 8 , comprising at least one kind of piperazine compound. 11. The acid gas absorbent according to claim 10 , wherein the piperazine compound is at least one selected from the group consisting of piperazine, 2-methylpiperazine, 2,5-dimethylpiperazine, and 2,6-dimethylpiperazine. 12. The acid gas absorbent according to claim 8 , wherein the alkanolamine and/or heterocyclic amine compound are selected from monoethanolamine, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1,3-propanediol, methylaminoethanol, diethanolamine, bis(2-hydroxy-1-methylethyl)amine, methyldiethanolamine, dimethylethanolamine, diethylethanolamine, triethanolamine, dimethylamino-1-methylethanol, 2-methylaminoethanol, 2-(ethylamino)ethanol, 2-propylaminoethanol, n-butylaminoethanol, 2-(isopropylamino)ethanol, 3-ethylaminopropanol, azetidine, 1-methylazetidine, 1-ethylazetidine, 2-methylazetidine, 2-azetidylmethanol, 2-(2-aminoethyl)azetidine, pyrrolidine, 1-methylpyrrolidine, 2-methylpyrrolidine, 2-butylpyrrolidine, 2-pyrrolidylmethanol, 2-(2-aminoethyl)pyrrolidine, piperidine, 1-methylpiperidine, 2-ethylpiperidine, 3-propylpiperidine, 4-ethylpiperidine, 2-piperidylmethanol, 3-piperidylethanol, 2-(2-aminoethyl)pyrrolidine, hexahydro-1H-azepine, hexamethylenetetramine, piperazine, 2-methylpiperazine, 2,5-dimethyl piperazine, and 2,6-dimethylpiperazine. 13. An acid gas removal method comprising: bringing gas containing acid gas into contact with the acid gas absorbent according to claim 1 to thereby remove the acid gas from the gas containing the acid gas. 14. The acid gas removal method according to claim 13 , wherein the acid gas is carbon dioxide.
Carbon dioxide · CPC title
Flue gases · CPC title
Removing carbon dioxide · CPC title
Hydrogen sulfide · CPC title
Glycols, diols or their derivatives · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.