Method and apparatus for sustainable carbon dioxide sequestration
US-2024424442-A1 · Dec 26, 2024 · US
US9713790B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9713790-B2 |
| Application number | US-201314140063-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 24, 2013 |
| Priority date | Aug 21, 2013 |
| Publication date | Jul 25, 2017 |
| Grant date | Jul 25, 2017 |
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Disclosed are a compound including an oxalate, a carbon dioxide absorbent including the same, a method of preparing the carbon dioxide absorbent and a method of removing carbon dioxide, which may overcome issues of high recycling energy and low absorptivity of a conventional carbon dioxide absorbent to considerably reduce recycling energy and absorb a greater amount of carbon dioxide per unit absorbent, so that a size of a carbon dioxide absorption tower may be reduced and a less amount of recycling energy may be used, contributing to a substantial decrease in device manufacture costs and management costs.
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What is claimed is: 1. A compound comprising: a divalent metal ion; an oxalate; and an amine ligand; wherein the divalent metal ion comprises magnesium, and wherein the amine ligand comprises at least one selected from the group consisting of monoethanolamine (MEA), diethanolamine (DEA), triethanolamine, methylmonoethanolamine, methyldiethanolamine, dimethylmonoethanolamine, diethylmonoethanolamine, monoisopropanolamine, diisopropanolamine, piperazine, 1-methylpiperazine, 2-methylpiperazine, dimethylpiperazine, 1-ethylpiperazine, 1-(2-aminoethyl)piperazine, 1-(2-hydroxyethyl)piperazine, 2-piperidinemethanol, 2-piperidineethanol, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-butanol, 2-amino-2-ethyl-1-propanediol, 3-aminopropanol, 2-ethylaminoethanol, 2-methylaminoethanol and 2-diethylaminoethanol. 2. The compound of claim 1 , wherein the divalent metal ion is present, in the compound, in an amount of 10% by weight (wt %) to 50 wt %. 3. The compound of claim 1 , wherein the oxalate is present, in the compound, in an amount of 45 wt % to 70 wt %. 4. The compound of claim 1 , wherein the amine ligand is present, in the compound, in an amount of 35 wt % to 60 wt %. 5. A carbon dioxide absorbent comprising: the compound of any one of claim 1 , 2 , 3 or 4 ; and an organic solvent. 6. The carbon dioxide absorbent of claim 5 , wherein the organic solvent comprises at least one selected from the group consisting of ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, diethylene glycol, dipropylene glycol and triethylene glycol. 7. A method of preparing a carbon dioxide absorbent, the method comprising: preparing the compound of claim 1 ; and mixing the compound and an organic solvent. 8. A method of removing carbon dioxide, the method comprising: bringing a gas comprising carbon dioxide into contact with the carbon dioxide absorbent of any one of claim 1 , 2 , 3 or 4 ; absorbing carbon dioxide from the gas; and recycling the carbon dioxide absorbent. 9. The method of claim 8 , wherein the absorbing of the carbon dioxide is carried out at a pressure in a range of atmospheric pressure to 10 atmospheres (atm), and at a temperature in a range of room temperature to 70° C. 10. The method of claim 8 , wherein the recycling of the carbon dioxide absorbent is carried out at a pressure in a range of atmospheric pressure to 5 atm, and at a temperature in a range of 80° C. to 150° C. 11. The carbon dioxide absorbent of claim 5 , wherein the organic solvent comprises ethylene glycol.
Other nitrogen compounds · CPC title
Removing carbon dioxide · CPC title
Selection of liquid materials for use as absorbents · CPC title
Flue gases · CPC title
Carbon oxides · CPC title
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