Compound including oxalate, carbon dioxide absorbent including the same, method of preparing carbon dioxide absorbent and method of removing carbon dioxide

US2015056114A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2015056114-A1
Application numberUS-201314140063-A
CountryUS
Kind codeA1
Filing dateDec 24, 2013
Priority dateAug 21, 2013
Publication dateFeb 26, 2015
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

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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.

First claim

Opening claim text (preview).

What is claimed is: 1 . A compound comprising: a divalent metal ion; an oxalate; and an amine ligand. 2 . The compound of claim 1 , wherein the compound is represented by Formula 1 or Formula 2: where M 2+ is the divalent metal ion and R is independently H or CH 3 . 3 . The compound of claim 1 , wherein the divalent metal ion comprises at least one selected from the group consisting of magnesium, calcium, nickel, zinc, strontium, barium, iron, copper, cobalt, lead and manganese. 4 . The compound of claim 1 , 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, triethylenetetramine, N,N′-Bis(3-aminopropyl)ethylenediamine, 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-ehtylaminoethanol, 2-methylaminoethanol and 2-diethylaminoethanol. 5 . 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 %. 6 . The compound of claim 1 , wherein the oxalate is present, in the compound, in an amount of 45 wt % to 70 wt %. 7 . The compound of claim 1 , wherein the amine ligand is present, in the compound, in an amount of 35 wt % to 60 wt %. 8 . A carbon dioxide absorbent comprising: the compound of any one of claims 1 to 7 ; and an organic solvent. 9 . The carbon dioxide absorbent of claim 8 , 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. 10 . A method of preparing a carbon dioxide absorbent, the method comprising: preparing a compound comprising a divalent metal ion, an oxalate and an amine ligand; and mixing the compound and an organic solvent. 11 . The method of claim 10 , wherein the divalent metal ion comprises at least one selected from the group consisting of magnesium, calcium, nickel, zinc, strontium, barium, iron, copper, cobalt, lead and manganese. 12 . The method of claim 10 , 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, triethylenetetramine, N,N′-Bis(3-aminopropyl)ethylenediamine, 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-ehtylaminoethanol, 2-methylaminoethanol and 2-diethylaminoethanol. 13 . A method of removing carbon dioxide, the method comprising: bringing a gas comprising carbon dioxide into contact with a carbon dioxide absorbent comprising a compound comprising a divalent metal ion, an oxalate and an amine ligand and an organic solvent; absorbing carbon dioxide from the gas; and recycling the carbon dioxide absorbent. 14 . The method of claim 13 , 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. 15 . The method of claim 13 , 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.

Assignees

Inventors

Classifications

  • B01D53/62Primary

    Carbon oxides · CPC title

  • Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters · CPC title

  • Selection of liquid materials for use as absorbents · CPC title

  • Flue gases · CPC title

  • Removing carbon dioxide · CPC title

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What does patent US2015056114A1 cover?
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 a…
Who is the assignee on this patent?
Korea Energy Research Inst
What technology area does this patent fall under?
Primary CPC classification B01D53/62. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Thu Feb 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).