Carbon dioxide separation composition and carbon dioxide separation method

Abstract

To provide a carbon dioxide separation composition which is excellent in carbon dioxide desorption efficiency (desorption amount / absorption amount) and durability to nitrogen oxides, and a method for separating carbon dioxide.SOLUTION: A carbon dioxide separation method includes the step of bringing a gas mixture containing nitrogen oxides and carbon dioxide into contact with an amine compound represented by formula (2), and a carbon dioxide separation composition containing water, thereby enabling the carbon dioxide in the gas mixture to be absorbed. The amine compound absorbs and releases carbon dioxide. The water level is 20-95 wt.% relative to the total amount of the carbon dioxide separation composition.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates to a carbon dioxide separation composition for selectively separating carbon dioxide from a carbon dioxide-containing mixed gas, and a carbon dioxide separation method using the composition. [Background technology]

[0002] In recent years, due to the issue of global warming, carbon dioxide separation and capture has attracted attention, and the development of carbon dioxide absorbents has been actively pursued.

[0003] The most common carbon dioxide absorption liquid is a monoethanolamine aqueous solution. Monoethanolamine is inexpensive and easily available industrially, but it has the characteristic that the carbon dioxide absorbed at low temperatures does not dissipate unless it is heated to a high temperature of 120°C or higher. If the carbon dioxide dissipation temperature is raised above the boiling point of water, a lot of energy is required to capture the carbon dioxide due to the high latent heat and specific heat of water.

[0004] Therefore, efforts are being made to develop amines that have a lower carbon dioxide release temperature and require less carbon dioxide recovery energy than monoethanolamine. For example, N-methyldiethanolamine (Patent Document 1) has been proposed. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] Japan Special Publication No. 2006-528062 Summary of the Invention [Problem to be solved by the invention]

[0006] In recent years, there has been a demand for carbon dioxide absorption solutions with even better carbon dioxide emission efficiency (emission amount / absorption amount). Also, from the perspective of stable operation of carbon dioxide capture facilities, there is a demand for carbon dioxide absorption solutions that are less likely to produce precipitates even when nitrogen oxides are mixed in.

[0007] The present invention has been made in view of the above-mentioned problems, and its object is to provide a carbon dioxide separation composition that has excellent carbon dioxide emission efficiency (emission amount / absorption amount) and is less likely to produce precipitates even when nitrogen oxides are mixed in, and a carbon dioxide separation method. [Means for solving the problem]

[0008] As a result of extensive research to solve the above problems, the inventors of the present invention discovered that a carbon dioxide separation composition containing a specific amine compound has excellent carbon dioxide emission efficiency (emission amount / absorption amount) and is less likely to produce precipitates even when nitrogen oxides are mixed in, and have completed the present invention.

[0009] That is, the present invention resides in the following [1] to [8]. [1] The following general formula (1)

[0010] [ka]

[0011] [In the above general formula (1), R 1 ~R 3 each independently represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. and an amine compound represented by the following general formula (2):

[0012] [ka]

[0013] [In general formula (2), R 10 , R 11 , R 12 , R 13 and R 14 each independently represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, a hydroxyl group, a hydroxymethyl group, a 2-hydroxyethyl group, or an alkoxy group having 1 to 4 carbon atoms. a and b each independently represent 0 or 1, and satisfy the relationship a+b=1. R 15 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, a methoxymethyl group, a methoxyethoxymethyl group, or a 2-hydroxyethyl group.] A composition for separating carbon dioxide, comprising at least one amine compound selected from the group consisting of amine compounds represented by the formula:

[0014] [2] The carbon dioxide separation composition according to [1], characterized in that it contains a mixture of an amine compound represented by the general formula (1) and an amine compound represented by the general formula (2).

[0015] [3] The composition for carbon dioxide separation according to [2] above, characterized in that the mixing ratio of the amine compound represented by the general formula (1) to the amine compound represented by the general formula (2) is 0.1 to 99.9 parts by weight per 100 parts by weight of the amine compound represented by the general formula (1).

[0016] [4] The amine compound represented by the general formula (1) is 1-(2,3-dihydroxypropyl)-piperazine (R 1 =R 2 =R 3 = hydrogen atom), 1-(2,3-dihydroxypropyl)-4-methylpiperazine (R 1 = methyl group, R 2 =R 3 = hydrogen atom), 1-(2,3-dihydroxypropyl)-4-ethylpiperazine (R 1 = ethyl group, R 2 =R 3 = hydrogen atom), 1-(2,3-dihydroxypropyl)-4-propylpiperazine (R 1 = propyl group, R 2 =R 3 = hydrogen atom), 1-(2,3-dihydroxypropyl)-4-butylpiperazine (R 1 = butyl group, R 2 =R 3 = hydrogen atom), 1-(2-hydroxy-3-methoxypropyl)-piperazine (R 1 =R 2 = hydrogen atom, R 3 = methyl group), 1-(2-hydroxy-3-methoxypropyl)-4-methylpiperazine (R 1 = methyl group, R 2 = hydrogen atom, R 3 = methyl group), 1-(2-hydroxy-3-methoxypropyl)-4-ethylpiperazine (R 1 = ethyl group, R 2 = hydrogen atom, R 3 = methyl group), 1-(2-hydroxy-3-methoxypropyl)-4-propylpiperazine (R 1 = propyl group, R 2 = hydrogen atom, R 3 = methyl group), 1-(2-hydroxy-3-methoxypropyl)-4-butylpiperazine (R 1 = butyl group, R 2 = hydrogen atom, R 3 = methyl group), 1-(2,3-dimethoxypropyl)-piperazine (R 1 = hydrogen atom, R 2 = methyl group, R 3 = methyl group), 1-(2,3-dimethoxypropyl)-4-methylpiperazine (R 1 = methyl group, R 2 = methyl group, R 3 = methyl group), 1-(2,3-dimethoxypropyl)-4-ethylpiperazine (R 1 = ethyl group, R 2 = methyl group, R 3 = methyl group), 1-(2,3-dimethoxypropyl)-4-propylpiperazine (R 1 = propyl group, R 2= methyl group, R 3 = methyl group), and 1-(2,3-dimethoxypropyl)-4-butylpiperazine (R 1 = butyl group, R 2 = methyl group, R 3 The carbon dioxide separation composition according to [1] or [2] above, characterized in that it is at least one selected from the group consisting of (a) and (b) (a) and (c) (b).

[0017] [5] The amine compound represented by the general formula (2) is 1,4-diazabicyclo[2.2.2]octane-2-methanol (R 10 =R 11 =R 12 =R 13 =R 14 =R 15 = hydrogen atom, a = 0, b = 1).

[0018] [6] A carbon dioxide separation composition according to [1] or [2] above, further comprising water, wherein the concentration of the water is 20 to 95% by weight based on the total weight of the carbon dioxide separation composition.

[0019] [7] A carbon dioxide separation composition according to [1] or [2] above, further comprising water, wherein the concentration of the water is 30 to 95% by weight based on the total weight of the carbon dioxide separation composition.

[0020] [8] A method for separating carbon dioxide, comprising the step of contacting a gas containing carbon dioxide with the carbon dioxide separation composition described in any one of [1] to [7] above to absorb the carbon dioxide in the mixed gas. [Effects of the Invention]

[0021] The carbon dioxide separation composition of the present invention has a higher carbon dioxide emission efficiency (emission amount / absorption amount) than conventionally known materials, and enables the recovery and separation of carbon dioxide gas at lower temperatures (lower energy) than conventionally known materials, thereby reducing the environmental load (high energy efficiency).

[0022] Furthermore, the carbon dioxide separation composition of the present invention is characterized by a higher carbon dioxide absorption rate per unit time and a higher carbon dioxide emission rate per unit time than conventionally known materials, and has the effect of being able to absorb and separate large amounts of carbon dioxide at high speed. Therefore, the present invention is extremely useful industrially in that it can efficiently absorb and separate carbon dioxide emitted in large amounts from large-scale thermal power plants and the like.

[0023] Furthermore, the carbon dioxide separation composition of the present invention has the advantage that, compared to conventionally known materials, it is less likely to produce precipitates (presumably degradation products of the carbon dioxide separation composition) when a gas containing nitrogen oxides (typically nitrogen dioxide) is blown into it. Therefore, the carbon dioxide separation composition of the present invention has the effect of reducing the risk of solid deposition and pipe blockage in carbon dioxide separation equipment compared to conventionally known materials. DETAILED DESCRIPTION OF THE INVENTION

[0024] The present invention will be described in detail below. First, the carbon dioxide separation composition of the present invention will be described.

[0025] The carbon dioxide separation composition of the present invention is characterized by containing at least one amine compound selected from the group consisting of the amine compound represented by the above general formula (1) and the amine compound represented by the above general formula (2).

[0026] In the present invention, at least one amine compound selected from the group consisting of the amine compound represented by the above general formula (1) and the amine compound represented by the above general formula (2) plays a role in adsorbing and desorbing carbon dioxide.

[0027] The present invention relates to a carbon dioxide separation composition comprising at least one amine compound selected from the group consisting of an amine compound represented by the general formula (1) and an amine compound represented by the general formula (2). The carbon dioxide separation composition may be a carbon dioxide separation composition containing an amine compound represented by the general formula (1), a carbon dioxide separation composition containing an amine compound represented by the general formula (2), or a carbon dioxide separation composition containing a mixture of an amine compound represented by the general formula (1) and an amine compound represented by the general formula (2) (containing both the amine compound represented by the general formula (1) and the amine compound represented by the general formula (2)). However, the carbon dioxide separation composition of the present invention preferably contains both the amine compound represented by the general formula (1) and the amine compound represented by the general formula (2) in terms of excellent carbon dioxide separation performance.

[0028] When the carbon dioxide separation composition of the present invention contains both the amine compound represented by the general formula (1) and the amine compound represented by the general formula (2), the mixing ratio of the amine compound represented by the general formula (1) to the amine compound represented by the general formula (2) is not particularly limited. However, in terms of excellent carbon dioxide separation performance, the mixing ratio of the amine compound represented by the general formula (2) to 100 parts by weight of the amine compound represented by the general formula (1) is preferably 0.1 to 99.9 parts by weight, more preferably 1 to 90 parts by weight, more preferably 1 to 75 parts by weight, even more preferably 5 to 50 parts by weight, and particularly preferably 10 to 30 parts by weight.

[0029] In the present invention, R 1 ~R 3 each independently represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.

[0030] The alkyl group having 1 to 4 carbon atoms is not particularly limited, but examples thereof include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, and a tertiary butyl group.

[0031] The aforementioned R 1 With regard to the carbon dioxide dissipation efficiency (amount dissipated / amount absorbed), it is preferably a hydrogen atom, a methyl group, an ethyl group, or a butyl group, more preferably a hydrogen atom or a methyl group, and even more preferably a hydrogen atom, in terms of excellent carbon dioxide dissipation efficiency (amount dissipated / amount absorbed).

[0032] The aforementioned R 2 or R 3 Regarding the groups, in terms of excellent carbon dioxide emission efficiency (emission amount / absorption amount), it is preferable that they are each independently a hydrogen atom, a methyl group, an ethyl group, or a butyl group, more preferably each independently a hydrogen atom or a methyl group, and even more preferably a hydrogen atom.

[0033] In the present invention, specific examples of the amine compound represented by the above general formula (1) include 1-(2,3-dihydroxypropyl)-piperazine (R 1 =R 2 =R 3 = hydrogen atom), 1-(2,3-dihydroxypropyl)-4-methylpiperazine (R 1 = methyl group, R 2 =R 3 = hydrogen atom), 1-(2,3-dihydroxypropyl)-4-ethylpiperazine (R 1 = ethyl group, R 2 =R 3 = hydrogen atom), 1-(2,3-dihydroxypropyl)-4-propylpiperazine (R 1 = propyl group, R 2 =R 3 = hydrogen atom), 1-(2,3-dihydroxypropyl)-4-butylpiperazine (R 1 = butyl group, R 2 =R 3 = hydrogen atom), 1-(2-hydroxy-3-methoxypropyl)-piperazine (R 1=R 2 = hydrogen atom, R 3 = methyl group), 1-(2-hydroxy-3-methoxypropyl)-4-methylpiperazine (R 1 = methyl group, R 2 = hydrogen atom, R 3 = methyl group), 1-(2-hydroxy-3-methoxypropyl)-4-ethylpiperazine (R 1 = ethyl group, R 2 = hydrogen atom, R 3 = methyl group), 1-(2-hydroxy-3-methoxypropyl)-4-propylpiperazine (R 1 = propyl group, R 2 = hydrogen atom, R 3 = methyl group), 1-(2-hydroxy-3-methoxypropyl)-4-butylpiperazine (R 1 = butyl group, R 2 = hydrogen atom, R 3 = methyl group), 1-(2,3-dimethoxypropyl)-piperazine (R 1 = hydrogen atom, R 2 = methyl group, R 3 = methyl group), 1-(2,3-dimethoxypropyl)-4-methylpiperazine (R 1 = methyl group, R 2 = methyl group, R 3 = methyl group), 1-(2,3-dimethoxypropyl)-4-ethylpiperazine (R 1 = ethyl group, R 2 = methyl group, R 3 = methyl group), 1-(2,3-dimethoxypropyl)-4-propylpiperazine (R 1 = propyl group, R 2 = methyl group, R 3 = methyl group), or 1-(2,3-dimethoxypropyl)-4-butylpiperazine (R 1 = butyl group, R 2 = methyl group, R 3 = methyl group).

[0034] Regarding the amine compound represented by the above general formula (1), from the viewpoint of availability, the amine compound represented by the following formula, i.e., 1-(2,3-dihydroxypropyl)-piperazine (in the above general formula (1), R 1 =R 2 =R 3 = hydrogen atom, hereinafter also referred to as DHPP).

[0035] [ka]

[0036] In the present invention, the amine compound represented by the general formula (1) may be a commercially available product or may be synthesized by a known method, and is not particularly limited. The purity of the amine compound represented by the general formula (1) is not particularly limited, but is preferably 95% by weight or more, and particularly preferably 99% by weight or more.

[0037] The above-mentioned 1-(2,3-dihydroxypropyl)-piperazine can be produced by reacting piperazine with 2,3-dihydroxychloropropane.

[0038] In the present invention, R 10 , R 11 , R 12 , R 13 , and R 14 each independently represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, a hydroxyl group, a hydroxymethyl group, a 2-hydroxyethyl group, or an alkoxy group having 1 to 4 carbon atoms.

[0039] In the present invention, R 10 , R 11 , R 12 , R 13 , and R 14are not particularly limited as long as they fall within the above definition, and examples of groups that can be independently selected include a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, a butyl group (an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group), a hydroxyl group, a hydroxymethyl group, a 2-hydroxyethyl group, a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, and a sec-butoxy group. Among these, a hydrogen atom, a methyl group, an ethyl group, a butyl group, a hydroxymethyl group, and a methoxy group are preferred in terms of excellent carbon dioxide diffusion efficiency.

[0040] In the present invention, R 15 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, a methoxymethyl group, a methoxyethoxymethyl group, or a 2-hydroxyethyl group.

[0041] In the present invention, R in the above general formula (2) 15 is not particularly limited as long as it satisfies the above definition, but examples thereof include a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, a butyl group (an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group), a methoxymethyl group, a methoxyethoxymethyl group, and a 2-hydroxyethyl group. Among these, a hydrogen atom, a methyl group, an ethyl group, a butyl group, a methoxymethyl group, a methoxyethoxymethyl group, and a 2-hydroxyethyl group are preferred in terms of excellent carbon dioxide diffusion efficiency.

[0042] Specific examples of the amine compound represented by the above general formula (2) include the following compounds (exemplary compounds 1 to 28), but the present invention is not limited to these.

[0043] [ka]

[0044] In the general formula (2), R10 , R 11 , R 12 , R 13 , R 14 , and R 15 With regard to the groups, it is preferable that they are each independently a hydrogen atom, a methyl group, an ethyl group, or a butyl group, and it is more preferable that they are each independently a hydrogen atom or a methyl group, in terms of excellent carbon dioxide diffusion efficiency (amount diffused / amount absorbed).

[0045] Furthermore, the above-mentioned R 10 , R 11 , R 12 , R 13 , R 14 , and R 15 is more preferably a hydrogen atom from the viewpoint of availability.

[0046] Regarding the amine compound represented by the above general formula (2), from the viewpoint of availability, 1,4-diazabicyclo[2.2.2]octane-2-methanol (R 10 =R 11 =R 12 =R 13 =R 14 =R 15 = hydrogen atom, a = 0, b = 1, and the above-mentioned exemplary compound 1 (hereinafter also referred to as DABCOM) is preferred.

[0047] In the present invention, the amine compound represented by the general formula (2) may be a commercially available product or may be synthesized by a known method, and is not particularly limited. Furthermore, the purity of the amine compound represented by the general formula (2) is not particularly limited, but is preferably 95% or more, and particularly preferably 99% or more. If the purity is less than 95%, the amount of carbon dioxide absorbed may decrease.

[0048] The amine compound represented by the general formula (2) is not particularly limited, but can be produced, for example, by a cyclization reaction of dihydroxyalkylpiperazines (e.g., 2,3-dihydroxypropylpiperazine) (see, for example, JP 2010-37325 A).

[0049] The carbon dioxide separation composition of the present invention, which contains at least one amine compound selected from the group consisting of the amine compounds represented by the general formula (1) and the amine compounds represented by the general formula (2), may further contain at least one amine compound (A) different from the amine compound selected from the group consisting of alkanolamines, propylenediamines, piperazines, piperidines, morpholines, pyrrolidines, azepanes, and polyethylenepolyamines, as long as the effects of the present invention are achieved. The coexistence of the alkanolamines, propylenediamines, piperazines, piperidines, morpholines, pyrrolidines, azepanes, or polyethylenepolyamines can increase the N atom content per unit weight of the carbon dioxide separation composition, and is expected to increase the carbon dioxide absorption per unit weight of the carbon dioxide separation composition.

[0050] Specific examples of the alkanolamines include ethanolamine, N-methylethanolamine, N,N-dimethylethanolamine, diethanolamine, N-methyldiethanolamine, N-(2-aminoethyl)ethanolamine, N-[2-(dimethylamino)ethyl],N-methylethanolamine, N-[2-(diethylamino)ethyl],N-ethylethanolamine, 2-(2-aminoethoxy)ethanol, 2-[2-(dimethylamino)ethoxy]ethanol, 2-[2-(diethylamino)ethoxy]ethanol, N-[2-(2-aminoethoxy)ethyl]ethanolamine, N-[2-{2-(dimethylamino)ethoxy}ethyl],N-methylethanolamine, and N-[2-{2-(diethylamino)ethoxy}ethyl],N-ethylethanolamine. Among these, from the viewpoints of availability and production costs, the alkanolamine is preferably at least one selected from the group consisting of ethanolamine, N-methyldiethanolamine, N-(2-aminoethyl)ethanolamine, and 2-(2-aminoethoxy)ethanol.

[0051] Specific examples of the propylene diamines include 1,3-propanediamine, 3-(dimethylamino)propylamine, 3-(diethylamino)propylamine, 1,3-bis(dimethylamino)propane, 1,3-bis(diethylamino)propane, etc. Among these, from the viewpoints of availability and production costs, the propylene diamine is preferably at least one selected from the group consisting of 1,3-propanediamine and 3-(dimethylamino)propylamine.

[0052] Specific examples of the piperazines include piperazine, 2-methylpiperazine, 1-(2-hydroxyethyl)-piperazine, 1-(2,3-dihydroxypropyl)-piperazine, 1-(2-hydroxyethyl)-4-methylpiperazine, 1-(2,3-dihydroxypropyl)-4-methylpiperazine, 1-(2,3-dihydroxypropyl)-4-ethylpiperazine, 1-(2,3-dihydroxypropyl)-4-propylpiperazine, 1-(2,3-dihydroxypropyl)-4-butylpiperazine, 1-(2-hydroxy-3-methoxypropyl)-piperazine, 1-(2-hydroxy-3-methoxypropyl)-4-methylpiperazine, 1-(2-hydroxy-3-meth 1-(2-hydroxypropyl)-4-ethylpiperazine, 1-(2-hydroxy-3-methoxypropyl)-4-propylpiperazine, 1-(2-hydroxy-3-methoxypropyl)-4-butylpiperazine, 1-(2,3-dimethoxypropyl)-piperazine, 1-(2,3-dimethoxypropyl)-4-methylpiperazine, 1-(2,3-dimethoxypropyl)-4-ethylpiperazine, 1-(2,3-dimethoxypropyl)-4-propylpiperazine, 1-(2,3-dimethoxypropyl)-4-butylpiperazine, 1,4-bis(2-hydroxyethyl)-piperazine, 1,4-bis(2,3-dihydroxypropyl)-piperazine, or 1,4-diazabicyclo[2.2.2]octane.

[0053] Specific examples of the piperidines include piperidine, 2-methylpiperidine, 1-(2,3-dihydroxypropyl)-piperidine, 1-(2,3-dihydroxypropyl)-4-methylpiperidine, 1-(2,3-dihydroxypropyl)-4-ethylpiperidine, 1-(2,3-dihydroxypropyl)-4-propylpiperidine, 1-(2,3-dihydroxypropyl)-4-butylpiperidine, 1-(2-hydroxy-3-methoxypropyl)-piperidine, 1-(2-hydroxy-3-methoxypropyl)-4-methylpiperidine, Examples thereof include 1-(2-hydroxy-3-methoxypropyl)-4-ethylpiperidine, 1-(2-hydroxy-3-methoxypropyl)-4-propylpiperidine, 1-(2-hydroxy-3-methoxypropyl)-4-butylpiperidine, 1-(2,3-dimethoxypropyl)-piperidine, 1-(2,3-dimethoxypropyl)-4-methylpiperidine, 1-(2,3-dimethoxypropyl)-4-ethylpiperidine, 1-(2,3-dimethoxypropyl)-4-propylpiperidine, and 1-(2,3-dimethoxypropyl)-4-butylpiperidine.

[0054] Specific examples of the morpholines include morpholine, 2-methylmorpholine, 2,6-dimethylmorpholine, 1-(2,3-dihydroxypropyl)-morpholine, 1-(2-hydroxy-3-methoxypropyl)-morpholine, and 1-(2,3-dimethoxypropyl)-morpholine.

[0055] Specific examples of the pyrrolidines include pyrrolidine, 2-methylpyrrolidine, 2,5-dimethylpyrrolidine, 1-(2,3-dihydroxypropyl)-pyrrolidine, 1-(2-hydroxy-3-methoxypropyl)-pyrrolidine, 1-(2,3-dimethoxypropyl)-pyrrolidine, and 1,5-diazabicyclo[4.3.0]-5-nonene.

[0056] Specific examples of the azepanes include azepane, 2-methylazepane, 2,7-dimethylazepane, and 1,8-diazabicyclo[5.4.0]-7-undecene.

[0057] Specific examples of the polyethylene polyamines include diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), pentaethylenehexamine (PEHA), hexaethyleneheptamine (HEHA), and polyethylene polyamines having eight or more amino groups.

[0058] Here, "TETA" refers to a compound in which four amino groups are connected in a linear or branched manner via an ethylene chain, but in the present invention, it also includes compounds that similarly have four amino groups and a piperazine ring structure. Specific examples of TETA compounds include 1,4,7,10-tetraazadecane, N,N-bis(2-aminoethyl)-1,2-ethanediamine, 1-[2-[(2-aminoethyl)amino]ethyl]-piperazine, and 1,4-bis(2-aminoethyl)-piperazine.

[0059] Furthermore, "TEPA" refers to a compound in which five amino groups are connected in a linear or branched manner via an ethylene chain, but in the present invention, it also includes compounds having five amino groups and a piperazine ring structure. Specific examples of TEPA compounds include 1,4,7,10,13-pentaazatridecane, N,N,N'-tris(2-aminoethyl)-1,2-ethanediamine, 1-[2-[2-[2-[(2-aminoethyl)amino]ethyl]amino]ethyl]piperazine, 1-[2-[bis(2-aminoethyl)amino]ethyl]piperazine, and bis[2-(1-piperazinyl)ethyl]amine.

[0060] Furthermore, "PEHA" refers to a compound in which six amino groups are connected in a linear or branched manner via an ethylene chain, but in the present invention, it also includes compounds that similarly have six amino groups and also have a piperazine ring structure. Specific compound names of PEHA include, for example, 1,4,7,10,13,16-hexaazahexadecane, N,N,N',N'-tetrakis(2-aminoethyl)-1,2-ethanediamine, N,N-bis(2-aminoethyl)-N'-[2-[(2-aminoethyl)amino]ethyl]-1,2-ethanediamine, 1-[2-[2-[2-[2-[(2-aminoethyl)amino]ethyl]amino]ethyl]amino]ethyl]-piperazine, 1-[2-[2-[2-[bis(2-aminoethyl)amino]ethyl]amino]ethyl]piperazine, and N,N'-bis[2-(1-piperazinyl)ethyl]-1,2-ethanediamine.

[0061] Furthermore, "HEHA" refers to a compound in which seven amino groups are connected in a linear or branched manner via an ethylene chain, but in the present invention, it also includes compounds having seven amino groups and a piperazine ring structure. Specific compound names of HEHA include, for example, 1,4,7,10,13,16,19-heptaazanonadecane, N-[2-[(2-aminoethyl)amino]ethyl]-N,N',N'-tris(2-aminoethyl)-1,2-ethanediamine, 1-[2-[2-[2-[2-[2-[2-[(2-aminoethyl)amino]ethyl]amino]ethyl]amino]ethyl]piperazine, and N-(2-aminoethyl)-N,N'-bis[2-(1-piperazinyl)ethyl]-1,2-ethanediamine.

[0062] Furthermore, "polyethylene polyamine having eight or more amino groups" refers to a compound in which eight or more amino groups are connected in a linear or branched manner via an ethylene chain, but in the present invention, it also includes compounds which similarly have eight or more amino groups and also have a piperazine ring structure. Specific examples of polyethylene polyamines having eight or more amino groups include the product name "Poly8" (manufactured by Tosoh Corporation) and polyethyleneimine.

[0063] Among these, from the viewpoint of availability and acquisition cost, diethylenetriamine (DETA) is preferred as polyethylene polyamines. triethylenetetramine (TETA), which consists of a mixture of 1,4,7,10-tetraazadecane, N,N-bis(2-aminoethyl)-1,2-ethanediamine, 1-[2-[(2-aminoethyl)amino]ethyl]-piperazine, and 1,4-bis(2-aminoethyl)-piperazine; tetraethylenepentamine (TEPA), which consists of a mixture of 1,4,7,10,13-pentaazatridecane, N,N,N'-tris(2-aminoethyl)-1,2-ethanediamine, 1-[2-[2-[2-[(2-aminoethyl)amino]ethyl]amino]ethyl]-piperazine, 1-[2-[bis(2-aminoethyl)amino]ethyl]-piperazine, and bis[2-(1-piperazinyl)ethyl]amine; pentaethylenehexamine (PEHA) consisting of a mixture of 1,4,7,10,13,16-hexaazahexadecane, N,N,N',N'-tetrakis(2-aminoethyl)-1,2-ethanediamine, N,N-bis(2-aminoethyl)-N'-[2-[(2-aminoethyl)amino]ethyl]-1,2-ethanediamine, 1-[2-[2-[2-[2-[(2-aminoethyl)amino]ethyl]amino]ethyl]amino]ethyl]-piperazine, 1-[2-[2-[2-[bis(2-aminoethyl)amino]ethyl]amino]ethyl]piperazine, and N,N'-bis[2-(1-piperazinyl)ethyl]-1,2-ethanediamine, Preferably, the compound is at least one selected from the group consisting of hexaethyleneheptamine (HEHA) consisting of a mixture of 1,4,7,10,13,16,19-heptaazanonadecane, N-[2-[(2-aminoethyl)amino]ethyl]-N,N',N'-tris(2-aminoethyl)-1,2-ethanediamine, 1-[2-[2-[2-[2-[2-[2-[(2-aminoethyl)amino]ethyl]amino]ethyl]amino]ethyl]amino]ethyl]-piperazine, and N-(2-aminoethyl)-N,N'-bis[2-(1-piperazinyl)ethyl]-1,2-ethanediamine, and a polyethylene polyamine having eight or more amino groups under the trade name "Poly8" (manufactured by Tosoh Corporation).

[0064] In the present invention, the alkanolamines, propylenediamines, piperazines, piperidines, morpholines, pyrrolidines, azepanes, or polyethylenepolyamines may be commercially available or synthesized by a known method, and are not particularly limited. Furthermore, the purity of the alkanolamines, propylenediamines, piperazines, piperidines, morpholines, pyrrolidines, azepanes, or polyethylenepolyamines is not particularly limited, but is preferably 95% by weight or more, particularly preferably 99% by weight or more.

[0065] When the carbon dioxide separation composition of the present invention contains both at least one amine compound selected from the group consisting of amine compounds represented by the general formula (1) and amine compounds represented by the general formula (2) above and at least one amine compound (A) selected from the group consisting of alkanolamines, propylenediamines, piperazines, piperidines, morpholines, pyrrolidines, azepanes, and polyethylenepolyamines, the weight ratio thereof is not particularly limited as long as it is within a range that achieves the effects of the present invention. Regarding this weight ratio, from the viewpoint of increasing the amount of carbon dioxide absorbed per unit weight, the content of amine compound (A) is preferably 0.1 to 99.9 parts by weight, more preferably 0.5 to 90 parts by weight, more preferably 1 to 75 parts by weight, even more preferably 1 to 50 parts by weight, and particularly preferably 5 to 40 parts by weight, per 100 parts by weight of at least one amine compound selected from the group consisting of amine compounds represented by the general formula (1) and amine compounds represented by the general formula (2) above.

[0066] The carbon dioxide separation composition of the present invention can be used as is for its intended purpose, but from the viewpoint of operability, it is usually preferable to use it as a solution further containing a solvent. The solvent used in the carbon dioxide separation composition is not particularly limited, but examples thereof include water, alcohol compounds, polyol compounds (e.g., ethylene glycol, glycerin, polyethylene glycol, etc., but are not particularly limited), and mixtures of these may also be used. Of these, water is preferred because of its excellent efficiency in absorbing and separating carbon dioxide gas as bicarbonate.

[0067] When the carbon dioxide separation composition of the present invention contains the above-mentioned solvent (e.g., water), the concentration of the solvent is preferably 20 to 95 wt %, more preferably 30 to 95 wt %, even more preferably 30 to 85 wt %, and particularly preferably 40 to 75 wt %, based on the total weight of the carbon dioxide separation composition, in order to improve the operability of the carbon dioxide separation composition.

[0068] In view of excellent durability against deterioration by nitrogen oxides, the carbon dioxide separation composition of the present invention is preferably a composition consisting of only water and at least one amine compound selected from the group consisting of the amine compounds represented by the general formula (1) and the amine compounds represented by the general formula (2). In this case, the preferred ranges of the compounds and the preferred ranges of the composition are as described above.

[0069] In the carbon dioxide separation composition comprising at least one amine compound selected from the group consisting of the amine compound represented by the general formula (1) and the amine compound represented by the general formula (2), the at least one amine compound selected from the group consisting of the amine compound represented by the general formula (1) and the amine compound represented by the general formula (2) is preferably the amine compound represented by the general formula (1) in that it increases the carbon dioxide absorption rate and absorption amount. That is, a carbon dioxide separation composition comprising the amine compound represented by the general formula (1) is preferred. For example, more specifically, a preferred carbon dioxide separation composition is prepared by dissolving the amine compound represented by the general formula (1) in a solvent such as water.

[0070] Hereinafter, a carbon dioxide separation composition containing an amine compound represented by the above general formula (1) will be described. In the carbon dioxide separation composition characterized by containing the amine compound represented by the general formula (1), the amine compound represented by the general formula (1) plays a role in adsorbing and desorbing carbon dioxide. In the carbon dioxide separation composition characterized by containing the amine compound represented by the general formula (1), the definition, preferred range, production method, etc. of the amine compound represented by the general formula (1) are as described above.

[0071] The carbon dioxide separation composition comprising the amine compound represented by the general formula (1) may further comprise, in addition to the amine compound represented by the general formula (1), at least one amine compound (A') selected from the group consisting of alkanolamines, propylene diamines, and polyethylene polyamines, as long as the effects of the present invention are achieved. The definition and preferred range of the propylene diamines or polyethylene polyamines in the amine compound (A') are as described above. The definition and preferred range of the alkanolamines in the amine compound (A') are as described below. In this case, the amine compound (A') does not include the amine compound represented by the general formula (1). The coexistence of the alkanolamines, propylene diamines, or polyethylene polyamines can increase the N atom content per unit weight of the carbon dioxide separation composition, and is expected to have the effect of increasing the carbon dioxide absorption per unit weight of the carbon dioxide separation composition.

[0072] In the carbon dioxide separation composition characterized by containing the amine compound represented by the general formula (1), specific examples of the alkanolamines include ethanolamine, N-methylethanolamine, N,N-dimethylethanolamine, diethanolamine, N-methyldiethanolamine, N-(2-aminoethyl)ethanolamine, N-[2-(dimethylamino)ethyl],N-methylethanolamine, N-[2-(diethylamino)ethyl],N-ethylethanolamine, 2-(2-aminoethoxy)ethanol, 2-[2-(dimethylamino)ethoxy]ethanol, 2-[2-(diethylamino)ethoxy]ethanol, N-[2-(2-aminoethoxy)ethyl]ethanolamine, N-[2-{2-(dimethylamino)ethoxy}ethyl],N-methylethanolamine, N-[2-{2-(diethylamino)ethoxy}ethyl],N-ethylethanolamine, or compounds of the following general formula (2):

[0073] [ka]

[0074] [In the formula, R 10 , R 11 , R 12 , R 13 and R 14 each independently represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, a hydroxyl group, a hydroxymethyl group, a 2-hydroxyethyl group, or an alkoxy group having 1 to 4 carbon atoms. a and b each independently represent 0 or 1, and satisfy the relationship a+b=1. R 15 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, a methoxymethyl group, a methoxyethoxymethyl group, or a 2-hydroxyethyl group.] Among these, from the viewpoints of availability and production costs, the alkanolamine is preferably at least one selected from the group consisting of ethanolamine, N-methyldiethanolamine, N-(2-aminoethyl)ethanolamine, 2-(2-aminoethoxy)ethanol, and the amine compound represented by the general formula (2) above.

[0075] The definition and preferred range of the amine represented by the general formula (2) are the same as the definition and preferred range of the amine represented by the general formula (2) above, but will be explained again below.

[0076] In the above general formula (2), R 10 , R 11 , R 12 , R 13 , and R 14are not particularly limited as long as they fall within the above definition, and examples of groups that can be independently selected include a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, a butyl group (an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group), a hydroxyl group, a hydroxymethyl group, a 2-hydroxyethyl group, a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an n-butoxy group, and a sec-butoxy group. Among these, a hydrogen atom, a methyl group, an ethyl group, a butyl group, a hydroxymethyl group, and a methoxy group are preferred in terms of excellent carbon dioxide diffusion efficiency.

[0077] In addition, R in the above general formula (2) 15 is not particularly limited as long as it satisfies the above definition, but examples thereof include a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, a butyl group (an n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group), a methoxymethyl group, a methoxyethoxymethyl group, and a 2-hydroxyethyl group. Among these, a hydrogen atom, a methyl group, an ethyl group, a butyl group, a methoxymethyl group, a methoxyethoxymethyl group, and a 2-hydroxyethyl group are preferred in terms of excellent carbon dioxide diffusion efficiency.

[0078] Specific examples of the amine compound represented by the above general formula (2) include the following compounds (exemplary compounds 1 to 28), but the present invention is not limited to these.

[0079] [ka]

[0080] The aforementioned R 10 , R 11 , R 12 , R 13 , R 14 , and R 15With regard to the groups, it is preferable that they are each independently a hydrogen atom, a methyl group, an ethyl group, or a butyl group, and it is more preferable that they are each independently a hydrogen atom or a methyl group, in terms of excellent carbon dioxide diffusion efficiency (amount diffused / amount absorbed).

[0081] The aforementioned R 10 , R 11 , R 12 , R 13 , R 14 , and R 15 is more preferably a hydrogen atom from the viewpoint of availability.

[0082] Regarding the amine compound represented by the above general formula (2), from the viewpoint of availability, 1,4-diazabicyclo[2.2.2]octane-2-methanol (R 10 =R 11 =R 12 =R 13 =R 14 =R 15 = hydrogen atom, a=0, b=1), that is, the above exemplary compound 1 is preferred.

[0083] In the carbon dioxide separation composition containing the amine compound represented by the general formula (1), the alkanolamines, propylenediamines, or polyethylenepolyamines may be commercially available or may be synthesized by a known method, and are not particularly limited. The purity of the alkanolamines, propylenediamines, or polyethylenepolyamines is not particularly limited, but is preferably 95% by weight or more, and particularly preferably 99% by weight or more.

[0084] When the carbon dioxide separation composition containing the amine compound represented by general formula (1) contains both the amine compound represented by general formula (1) and at least one amine compound (A') selected from the group consisting of alkanolamines, propylenediamines, and polyethylenepolyamines, the weight ratio thereof is not particularly limited. With regard to the weight ratio, from the viewpoint of increasing the amount of carbon dioxide absorbed per unit weight, the content of the amine compound (A') is preferably 0.1 to 99.9 parts by weight, more preferably 0.5 to 90 parts by weight, more preferably 1 to 75 parts by weight, even more preferably 1 to 50 parts by weight, and particularly preferably 5 to 40 parts by weight, per 100 parts by weight of the amine compound represented by general formula (1).

[0085] The carbon dioxide separation composition containing the amine compound represented by the general formula (1) can be used as is for its intended purpose, but from the viewpoint of operability, it is usually preferable to use it as a solution further containing a solvent. The solvent used in the carbon dioxide separation composition is not particularly limited, but examples thereof include water, alcohol compounds, polyol compounds (e.g., ethylene glycol, glycerin, polyethylene glycol, etc., but are not particularly limited), and mixtures of these may also be used. Of these, water is preferred because it is highly efficient in absorbing and separating carbon dioxide gas as bicarbonate, is excellent in suppressing increases in the viscosity of absorbents and separating agents and the generation of solids, and does not significantly increase the carbon dioxide emission energy.

[0086] When a solvent (e.g., water) is used, the concentration of the solvent is preferably 20 to 95 wt %, more preferably 30 to 95 wt %, even more preferably 30 to 85 wt %, and particularly preferably 40 to 75 wt %, relative to the total amount of the carbon dioxide separation composition, in order to provide excellent operability of the carbon dioxide separation composition characterized by containing the amine compound represented by the general formula (1) above.

[0087] In the carbon dioxide separation composition comprising at least one amine compound selected from the group consisting of the amine compound represented by the general formula (1) and the amine compound represented by the general formula (2), the at least one amine compound selected from the group consisting of the amine compound represented by the general formula (1) and the amine compound represented by the general formula (2) is preferred in terms of promoting carbon dioxide emission and increasing the emission efficiency (amount of carbon dioxide emitted / amount of carbon dioxide absorbed). That is, a carbon dioxide separation composition comprising the amine compound represented by the general formula (2) is preferred. For example, more specifically, a preferred carbon dioxide separation composition is prepared by dissolving the amine compound represented by the general formula (2) in a solvent such as water.

[0088] Hereinafter, a carbon dioxide separation composition containing an amine compound represented by the above general formula (2) will be described. In the carbon dioxide separation composition characterized by containing the amine compound represented by the general formula (2), the amine compound represented by the general formula (2) plays a role in promoting the release of carbon dioxide and increasing the release efficiency (amount of carbon dioxide released / amount of carbon dioxide absorbed). In the composition for carbon dioxide separation, which is characterized by containing the amine compound represented by the general formula (2), the definition, preferred range, production method, etc. of the amine compound represented by the general formula (2) are as described above.

[0089] A carbon dioxide separation composition characterized by containing an amine compound represented by the general formula (2) may further contain, in addition to the amine compound represented by the general formula (2), at least one amine compound (A) selected from the group consisting of alkanolamines, propylenediamines, piperazines, piperidines, morpholines, pyrrolidines, azepanes, and polyethylenepolyamines, as long as the effects of the present invention are achieved. The definition and preferred range of the amine compound (A) are as described above. In this case, the amine compound (A) does not include the amine compound represented by the general formula (2). The coexistence of the amine compound (A) can increase the N atom content per unit weight of the carbon dioxide separation composition, and is expected to have the effect of increasing the carbon dioxide absorption per unit weight of the carbon dioxide separation composition.

[0090] In the carbon dioxide separation composition characterized by containing the amine compound represented by the general formula (2), the amine compound (A) that may be contained may be a commercially available product or may be synthesized by a known method, and is not particularly limited. The purity of the amine compound (A) is not particularly limited, but is preferably 95% or higher, and particularly preferably 99% or higher. If the purity is lower than 95%, the amount of carbon dioxide absorbed may decrease.

[0091] In a carbon dioxide separation composition comprising an amine compound represented by the general formula (2), when the carbon dioxide separation composition contains the amine compound (A), the weight fraction of the amine compound represented by the general formula (2) and the amine compound (A) is not particularly limited. From the viewpoint of increasing the amount of carbon dioxide absorbed per unit weight, the weight fraction of the amine compound represented by the general formula (2) (assuming that the total of the amine compound represented by the general formula (2) and the amine compound (A) is 100% by weight) is preferably 50 to 99.9% by weight, more preferably 80 to 99% by weight.

[0092] A carbon dioxide separation composition containing an amine compound represented by the general formula (2) can be used as is for its intended purpose, but from the viewpoint of operability, it can also be used as a composition further containing a solvent. The solvent used in the carbon dioxide separation composition is not particularly limited, and examples thereof include water, alcohol compounds, and polyol compounds (e.g., ethylene glycol, glycerin, and polyethylene glycol, but are not particularly limited thereto), and mixtures of these may also be used. Of these, water is preferred because it is highly efficient in absorbing and separating carbon dioxide gas as bicarbonate, is excellent in suppressing increases in the viscosity of absorbents and separating agents and the generation of solids, and does not significantly increase the carbon dioxide emission energy.

[0093] When a solvent (e.g., water) is used, the concentration of the solvent is preferably 20 to 95 wt %, more preferably 30 to 95 wt %, even more preferably 30 to 85 wt %, and particularly preferably 50 to 80 wt %, relative to the total amount of the carbon dioxide separation composition, in order to provide excellent operability of the carbon dioxide separation composition characterized by containing the amine compound represented by the general formula (2) above.

[0094] Next, a method for separating carbon dioxide using the carbon dioxide separation composition of the present invention will be described.

[0095] The carbon dioxide separation method of the present invention is characterized by comprising a step of contacting the carbon dioxide separation composition described above with a gas containing carbon dioxide to allow the carbon dioxide to be highly selectively absorbed into the carbon dioxide separation composition, and may also comprise a step of, after such absorption, releasing the absorbed carbon dioxide by heating the carbon dioxide separation composition and / or exposing it to a reduced pressure environment.

[0096] In the carbon dioxide separation method of the present invention, the method for contacting a carbon dioxide-containing gas with the carbon dioxide separation composition is not particularly limited, and known methods can be used, such as a bubbling method and a head-on contact method using a packed column or a plate column.

[0097] In the carbon dioxide separation method of the present invention, the temperature at which the carbon dioxide-containing gas is absorbed into the carbon dioxide separation composition is not particularly limited, but can usually be in the range of 0°C to 50°C.

[0098] In the carbon dioxide separation method of the present invention, the temperature at which carbon dioxide is released from the carbon dioxide separation composition is not particularly limited, but is typically in the range of 60 to 150° C. However, from the viewpoint of energy conservation, it is preferably 100° C. or lower. The carbon dioxide separation composition can also be used as a carbon dioxide absorbing / releasing agent in a method for chemically absorbing carbon dioxide.

[0099] The chemical absorption method involves contacting the carbon dioxide separation composition with a gas containing carbon dioxide to absorb the carbon dioxide, and then dissipating the absorbed carbon dioxide by increasing the temperature or reducing the pressure. The temperature at which the carbon dioxide is dissipated is not particularly limited, but may be, for example, 60°C or higher, and is more preferably 80°C or higher, even more preferably 90°C or higher, and particularly preferably 100°C or higher, in terms of excellent dissipation efficiency. The carbon dioxide separating composition can also be supported on a carrier and used as a carbon dioxide absorbing / releasing agent.

[0100] The carrier is not particularly limited, but examples thereof include silica, alumina, magnesia, porous glass, activated carbon, polymethyl methacrylate-based porous resin, and fibers.

[0101] Known silicas include crystalline silica, non-crystalline (amorphous) silica, silica with fine pores (for example, mesoporous silica), etc. There are no particular restrictions on the silica that can be used in the carbon dioxide absorption / desorption agent, and any silica that is commercially available can be used, but silica with a large surface area is preferred.

[0102] The amount of the carbon dioxide separation composition supported in the carbon dioxide absorption / desorption agent is preferably 5 to 70 parts by weight, and more preferably 10 to 60 parts by weight, per 100 parts by weight of the carrier, in terms of excellent carbon dioxide absorption capacity and ease of supporting the carbon dioxide separation composition. The carbon dioxide absorbing and releasing agent may further contain water.

[0103] The carbon dioxide absorption / desorption agent can be applied to a carbon dioxide separation method widely known as a solid absorption method. The solid absorption method is a method in which a carbon dioxide absorption / desorption agent is brought into contact with a gas containing carbon dioxide to absorb carbon dioxide into the carbon dioxide absorption / desorption agent, and then the carbon dioxide absorbed by the agent is desorbed by heating the agent or exposing it to a reduced pressure environment. In this case, the temperature at which carbon dioxide is desorbed is not particularly limited, but may be, for example, 60°C or higher. In terms of excellent desorption efficiency, 80°C or higher is more preferable, 90°C or higher is even more preferable, and 100°C or higher is particularly preferable.

[0104] The carbon dioxide-containing gas may be pure carbon dioxide gas or a mixed gas containing carbon dioxide and other gases, such as, but not limited to, air, nitrogen, oxygen, hydrogen, argon, neon, helium, carbon monoxide, water vapor, methane, or nitrogen oxides.

[0105] There are no particular restrictions on the mixed gas that can be applied to the carbon dioxide separation method of the present invention, as long as it contains carbon dioxide. However, in order to improve the separation performance between carbon dioxide and other gases, it is preferable that the carbon dioxide concentration is 5% by volume or more, and more preferably 10% by volume or more.

[0106] In the carbon dioxide separation method of the present invention, there is no problem if additional steps other than the above steps (absorption step and diffusion step) are carried out. For example, a cooling step, a heating step, a washing step, an extraction step, an ultrasonic treatment step, a distillation step, or other steps of treating with chemicals can be carried out as appropriate.

[0107] The carbon dioxide separation method of the present invention is not particularly limited, but can be applied to, for example, the separation of carbon dioxide (CO2) from combustion exhaust gas generated in thermal power plants, steel plants, cement factories, etc., and the separation of carbon dioxide (CO2) from steam reformed gas obtained in a steam reforming process. [Example]

[0108] The present invention will be described below using examples, but the present invention should not be construed as being limited to these examples.

[0109] <Method for measuring carbon dioxide gas diffusion efficiency> 100 g of the carbon dioxide absorbing solution prepared in the Examples described below (contained in a 200 mL gas absorption bottle) was adjusted to 40°C in a water bath. A mixed gas (500 mL / min) of carbon dioxide gas at 100 mL / min and nitrogen gas at 400 mL / min was bubbled into this carbon dioxide absorbing solution for 1 hour. The amount of carbon dioxide gas absorbed during this process (CO2 absorption amount (L) per hour) was measured using a gas flow meter and a carbon dioxide concentration meter. The CO2 absorption amount (L) per 1 kg of carbon dioxide absorbing solution was calculated using this CO2 absorption amount (L) per hour.

[0110] Next, the temperature of this carbon dioxide absorbing solution was adjusted to 70°C in a water bath. Nitrogen gas was bubbled into this carbon dioxide absorbing solution at a rate of 500 mL / min for 2 hours. The amount of carbon dioxide gas released during this process (CO2 release amount (L) over 2 hours) was measured using a gas flow meter and a carbon dioxide concentration meter. The CO2 release amount (L) over 2 hours was used to calculate the CO2 release amount (L) per 1 kg of carbon dioxide absorbing solution.

[0111] The carbon dioxide gas emission efficiency (= CO2 emission amount (L) in 2 hours ÷ CO2 absorption amount (L) in 1 hour) was calculated from the CO2 emission amount (L) in 2 hours and the CO2 absorption amount (L) in 1 hour.

[0112] <How to check for the presence of precipitates due to the effects of nitrogen oxides> 100 g of carbon dioxide absorbing solution prepared in the Examples described below (contained in a 200 mL gas absorption bottle) was adjusted to 30°C in an oil bath. A mixed gas (666 mL / min) of carbon dioxide gas at 650 mL / min, nitrogen gas at 15.7 mL / min, and nitrogen dioxide (NO) gas at 0.32 mL / min was bubbled into the carbon dioxide absorbing solution for 32 hours. The carbon dioxide absorbing solution was then heated in a 105°C oil bath and refluxed for 1 hour. The carbon dioxide absorbing solution was then cooled to 30°C, and the water lost during the refluxing process was replenished. The above procedure of gas injection for 32 hours, heating and refluxing, and cooling / water replenishment was repeated a total of seven times, and the contents of the gas absorption bottle were visually inspected. <Materials used in evaluation> The abbreviations and structures of the compounds used in the following experiments are shown below.

[0113] PIP: Piperazine (Sigma-Aldrich) DHPP: 1-(2,3-dihydroxypropyl)-piperazine (Sigma-Aldrich) DABCOM: 1,4-diazabicyclo[2,2,2]octane-2-methanol (Tosoh Corporation) MDEA: N-methyldiethanolamine (Fujifilm Wako Pure Chemical Industries, Ltd.)

[0114] [ka]

[0115] [Example 1] 30 g of DHPP was mixed with 70 g of pure water and stirred to prepare a carbon dioxide absorption solution (100 g). This was then placed in a 200 mL gas absorption bottle to measure the carbon dioxide gas diffusion efficiency and to check for the occurrence of precipitates due to the influence of nitrogen oxides.

[0116] The amount of CO2 absorbed (L) per hour was 2.45 L converted to standard conditions. In other words, the amount of CO2 absorbed (L) per hour per 1 kg of carbon dioxide absorbing solution was 24.5 L converted to standard conditions. The amount of CO2 absorbed per unit time per hour (mL / min) per 1 kg of carbon dioxide absorbing solution was 409 mL / min (= 24.5 [L / hr] x 1000 [mL / L] ÷ 60 [min / hr]).

[0117] The CO2 emission amount (L) over two hours was 1.24 L converted to standard conditions. In other words, the CO2 emission amount (L) over two hours per 1 kg of carbon dioxide absorbing solution was 12.4 L converted to standard conditions. The CO2 emission amount (mL / min) over two hours per unit time per 1 kg of carbon dioxide absorbing solution was 103 mL / min (= 12.4 [L / 2 hours] × 1000 [mL / L] ÷ 120 [min / hour]).

[0118] The carbon dioxide gas emission efficiency (= CO2 emission amount (L) over 2 hours ÷ CO2 absorption amount (L) over 1 hour) was 0.51. No precipitates were formed due to the influence of nitrogen oxides. The results are shown in Table 1.

[0119] [Example 2] A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 32.6 g of DHPP, 7.4 g of DABCOM, and 60 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 1.

[0120] [Example 3] A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 50.0 g of DHPP, 7.4 g of DABCOM, and 42.6 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 1.

[0121] [Example 4] 30 g of DABCOM and 70 g of pure water were mixed and stirred to prepare a carbon dioxide absorbing solution (100 g), and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 1.

[0122] [Example 5] A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 36.7 g of DHPP, 8.3 g of DABCOM, and 55 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 2.

[0123] [Example 6] A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 28.6 g of DHPP, 6.4 g of DABCOM, and 65 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 2.

[0124] [Example 7] A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 24.5 g of DHPP, 5.5 g of DABCOM, and 70 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 2.

[0125] [Example 8] A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 40.8 g of DHPP, 9.2 g of DABCOM, and 50 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 2.

[0126] [Example 9] A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 34.7 g of DHPP, 7.8 g of DABCOM, and 57.5 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 2.

[0127] [Example 10] A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 38.8 g of DHPP, 8.7 g of DABCOM, and 52.5 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 2.

[0128] [Comparative Example 1] 30 g of MDEA and 70 g of pure water were mixed and stirred to prepare a carbon dioxide absorbing solution (100 g), and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 1.

[0129] Comparative Example 2 A carbon dioxide absorbing solution (100 g) was prepared by mixing and stirring 32.6 g of MDEA, 7.4 g of PIP, and 60 g of pure water, and the carbon dioxide gas diffusion efficiency was measured and the occurrence of precipitates due to the influence of nitrogen oxides was confirmed in the same manner as in Example 1. The evaluation results are shown in Table 1.

[0130] [Table 1]

[0131] [Table 2]

[0132] As described in the above examples, the carbon dioxide separation composition of the present invention has superior carbon dioxide emission efficiency (emission amount / absorption amount) compared to conventionally known carbon dioxide separation compositions, and is less likely to produce precipitates even when nitrogen oxides are mixed in.

[0133] Although the present invention has been described in detail and with reference to specific embodiments, it will be apparent to those skilled in the art that various changes and modifications can be made without departing from the spirit and scope of the invention.

[0134] The entire contents of the specifications, claims, drawings and abstracts of Japanese Patent Application No. 2020-011936 filed on January 28, 2020, Japanese Patent Application No. 2020-049127 filed on March 19, 2020, and Japanese Patent Application No. 2020-110107 filed on June 26, 2020 are hereby incorporated by reference as the disclosure of the specification of the present invention. [Industrial Applicability]

[0135] The composition of the present invention can be used for separating and purifying carbon dioxide from combustion exhaust gases generated at thermal power plants, steel plants, cement factories, etc., and for separating and purifying carbon dioxide from steam reformed gas obtained in a steam reforming process.

Claims

1. The following formula 【Chemistry 1】 and water, wherein the amine compound plays a role in absorbing and releasing carbon dioxide, and the concentration of the water is 20 to 95% by weight. The carbon dioxide separation composition is contacted with a mixed gas containing nitrogen oxides and carbon dioxide, thereby allowing the carbon dioxide in the mixed gas to be absorbed by the carbon dioxide separation composition.

2. A method for separating carbon dioxide as described in claim 1, wherein the concentration of the water is 30 to 95% by weight relative to the total amount of the carbon dioxide separation composition.

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