Acid gas absorbent, acid gas removal method, and acid gas removal device

US9409119B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9409119-B2
Application numberUS-201113332018-A
CountryUS
Kind codeB2
Filing dateDec 20, 2011
Priority dateDec 22, 2010
Publication dateAug 9, 2016
Grant dateAug 9, 2016

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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An acid gas absorbent of which recovery amount of acid gas such as carbon dioxide is high, and an acid gas removal device and an acid gas removal method using the acid gas absorbent are provided. The acid gas absorbent of the embodiment comprising at least one type of tertiary amine compound represented by the following general formula (1). (In the above-stated formula (1), either one of the R 1 , R 2 represents a substituted or non-substituted alkyl group of which carbon number is 2 to 5, and the other one represents a substituted or non-substituted alkyl group of which carbon number is 1 to 5. The R 3 represents a methyl group or an ethyl group, and the R 4 represents a hydroxyalkyl group. The R 1 , R 2 may either be the same or different, and they may be coupled to form a cyclic structure.)

First claim

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What is claimed is: 1. An acid gas absorbent comprising at least one type of tertiary amine compound represented by the following general formula (1): wherein the R 3 represents a methyl group or an ethyl group, and the R 4 represents a hydroxyalkyl group; R 1, R 2 are coupled to form a cyclopentyl group; and wherein a content of the tertiary amine compound represented by the general formula (1) is 10 mass % to 55 mass %. 2. The acid gas absorbent according to claim 1 , wherein the R 4 is a 2-hydroxyethyl group in the tertiary amine compound represented by the general formula (1). 3. The acid gas absorbent according to claim 1 , further comprising a reaction accelerator consisting of alkanolamines and/or a hetero cyclic amine compound represented by the following general formula (2), wherein a content of the reaction accelerator is 1 mass % to 20 mass %: wherein the R 5 represents a hydrogen atom or a substituted or non-substituted alkyl group having a carbon number from 1 to 4, the R 6 represents a substituted or non-substituted alkyl group having a carbon number from 1 to 4 coupled to a carbon atom; the “n” represents an integer from 1 to 3, the “m” represents an integer from 1 to 4, and the “p” represents an integer from “0” (zero) to 12; when the “n” is 2 to 3, the nitrogen atoms are not directly coupled with each other. 4. The acid gas absorbent according to claim 3 , wherein the alkanolamines are at least one type selected from a group consisting of 2-(isopropylamino)ethanol, 2-(ethylamino)ethanol, and 2-amino-2-methyl-1-propanol. 5. The acid gas absorbent according to claim 3 , wherein the hetero cyclic amine compound includes at least one type selected from a group of piperazines. 6. The acid gas absorbent according to claim 5 , wherein the piperazines are at least one type selected from a group consisting of piperazine, 2-methylpiperazine, 2,5-dimethylpiperazine, and 2,6-dimethylpiperazine. 7. An acid gas absorbent comprising at least one type of secondary amine compound represented by the following general formula (4): wherein the R 12 represents a hydroxyalkyl group; the R 10 , R 11 are coupled to form a cyclopentyl group; wherein a content of the secondary amine compound represented by the general formula (4) is 10 mass % to 55 mass %. 8. The acid gas absorbent according to claim 7 , wherein the R 12 is a 2-hydroxyethyl group in the secondary amine compound represented by the general formula (4). 9. The acid gas absorbent according to claim 7 , further comprising a reaction accelerator consisting of alkanolamines and/or a hetero cyclic amine compound represented by the following general formula (2), wherein a content of the reaction accelerator is 1 mass % to 20 mass %: wherein the R 5 represents a hydrogen atom or a substituted or non-substituted alkyl group having a carbon number from 1 to 4, the R 6 represents a substituted or non-substituted alkyl group having a carbon number from 1 to 4 coupled to a carbon atom; the “n” represents an integer from 1 to 3, and the “m” represents an integer from 1 to 4, and the “p” represents an integer from “0” (zero) to 12; when the “n” is 2 to 3, the nitrogen atoms are not directly coupled with each other. 10. The acid gas absorbent according to claim 9 , wherein the alkanolamines are at least one type selected from a group consisting of 2-(isopropylamino)ethanol, 2-(ethylamino)ethanol, and 2-amino-2-methyl-1-propanol. 11. The acid gas absorbent according to claim 9 , wherein the hetero cyclic amine compound includes at least one type selected from a group of piperazines. 12. The acid gas absorbent according to claim 11 , wherein the piperazines are at least one type selected from a group consisting of piperazine, 2-methylpiperazine, 2,5-dimethylpiperazine, 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 remove the acid gas from the gas containing the acid gas. 14. An acid gas removal method, comprising: bringing gas containing acid gas into contact with the acid gas absorbent according to claim 3 to remove the acid gas from the gas containing the acid gas. 15. An acid gas removal method, comprising: bringing gas containing acid gas into contact with the acid gas absorbent according to claim 7 to remove the acid gas from the gas containing the acid gas. 16. An acid gas removal method, comprising: bringing gas containing acid gas into contact with the acid gas absorbent according to claim 9 to remove the acid gas from the gas containing the acid gas. 17. An acid gas removal device removing acid gas from gas containing the acid gas, comprising: an absorption tower bringing the gas containing the acid gas into contact with the acid gas absorbent according to claim 1 to remove the acid gas from the gas; and a regeneration tower removing the acid gas from the acid gas absorbent absorbing the acid gas and regenerating the acid gas absorbent to be reused at the absorption tower. 18. An acid gas removal device removing acid gas from gas containing the acid gas, comprising: an absorption tower bringing the gas containing the acid gas into contact with the acid gas absorbent according to claim 3 to remove the acid gas from the gas; and a regeneration tower removing the acid gas from the acid gas absorbent absorbing the acid gas and regenerating the acid gas absorbent to be reused at the absorption tower. 19. An acid gas removal device removing acid gas from gas containing the acid gas, comprising: an absorption tower bringing the gas containing the acid gas into contact with the acid gas absorbent according to claim 7 to remove the acid gas from the gas; and a regeneration tower removing the acid gas from the acid gas absorbent absorbing the acid gas and regenerating the acid gas absorbent to be reused at the absorption tower. 20. An acid gas removal device removing acid gas from gas containing the acid gas, comprising: an absorption tower bringing the gas containing the acid gas into contact with the acid gas absorbent according to claim 9 to remove the acid gas from the gas; and a regeneration tower removing the acid gas from the acid gas absorbent absorbing the acid gas and regenerating the acid gas absorbent to be reused at the absorption tower.

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What does patent US9409119B2 cover?
An acid gas absorbent of which recovery amount of acid gas such as carbon dioxide is high, and an acid gas removal device and an acid gas removal method using the acid gas absorbent are provided. The acid gas absorbent of the embodiment comprising at least one type of tertiary amine compound represented by the following general formula (1). (In the above-stated formul…
Who is the assignee on this patent?
Murai Shinji, Maezawa Yukishige, Kato Yasuhiro, and 7 more
What technology area does this patent fall under?
Primary CPC classification B01D53/1493. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Aug 09 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).