Carbon Dioxide Absorbing Composition, Method of Absorbing Carbon Dioxide and Method of Separating Carbon Dioxide Using the Same

Abstract

Provided are a carbon dioxide absorbing composition comprising an ionic material comprising a cyclic ammonium cation and a method of separating carbon dioxide using the same, and the carbon dioxide absorbing composition of the present disclosure has high thermal and chemical stability and excellent carbon dioxide absorption effect. In addition, the method of separating carbon dioxide using the carbon dioxide absorbing composition is very effective for desorption of carbon dioxide, and is a very economical method since it allows repeated use of the carbon dioxide absorbing composition.

Claims

1. A carbon dioxide absorbing composition comprising an ionic material comprising a cyclic ammonium cation represented by the following Chemical Formula 1: ##STR00022## wherein L.sub.1 is a single bond, O, NR.sub.7, or (C1-C8)alkylene, R.sub.1 to R.sub.4 are each independently of one another hydrogen or (C1-C10)alkyl, and R.sub.5 to R.sub.7 are each independently of one another (C1-C20)alkyl or hydroxy(C1-C20)alkyl, or R.sub.5 and R.sub.7 may be bonded to each other to form a ring.

2. The carbon dioxide absorbing composition of claim 1, wherein the cyclic ammonium cation is represented by the following Chemical Formula 2: ##STR00023## wherein L.sub.1 is a single bond, O, NR.sub.7, or (C1-C5)alkylene, and R.sub.5 to R.sub.7 are each independently of one another (C1-C10)alkyl or hydroxy(C1-C10)alkyl, or R.sub.5 and R.sub.7 may be bonded to each other to form (C1-10)heterocycloalkyl.

3. The carbon dioxide absorbing composition of claim 2, wherein L.sub.1 is a single bond, O, NR.sub.7, or (C1-C3)alkylene, R.sub.5 and R.sub.6 are each independently of each other (C1-C5)alkyl or hydroxy(C1-C5)alkyl, and R.sub.7 is (C1-C5)alkyl.

4. The carbon dioxide absorbing composition of claim 2, wherein L.sub.1 is a single bond, O, NR.sub.7, or methylene, R.sub.5 and R.sub.6 are each independently of each other methyl, butyl, or hydroxy(C2-C3)alkyl, and R.sub.7 is methyl.

5. The carbon dioxide absorbing composition of claim 1, wherein the cyclic ammonium cation is represented by the following Chemical Formula 3: ##STR00024## wherein L.sub.2 is (C1-C10)alkylene, R.sub.1 to R.sub.4 are each independently of one another hydrogen or (C1-C5)alkyl, and R.sub.6 is (C1-C10)alkyl or hydroxy(C1-C10)alkyl.

6. The carbon dioxide absorbing composition of claim 5, wherein L.sub.2 is (C1-C5)alkylene, R.sub.1 to R.sub.4 are each independently of one another hydrogen or (C1-C3)alkyl, and R.sub.6 is (C1-C5)alkyl or hydroxy(C1-C5)alkyl.

7. The carbon dioxide absorbing composition of claim 5, wherein L.sub.2 is ethylene, R.sub.1 to R.sub.4 are hydrogen, and R.sub.6 is butyl or propanol.

8. The carbon dioxide absorbing composition of claim 1, wherein the ionic material further comprises a phenolate-based anion represented by the following Chemical Formula 4 and/or an imidazolate-based anion represented by the following Chemical Formula 5: ##STR00025## wherein R.sub.21 to R.sub.25 are each independently of one another hydrogen, amino, hydroxy, nitro, carboxamido, C1-C10 alkyl, C1-C10 alkoxy, C1-C10 alkylcarbonyl, C1-C10 alkoxycarbonyl, C1-C10 alkylamino, diC1-C10 alkylamino, C1-C10 alkylaminoC1-C10 alkyl, or diC1-C10 alkylaminoC1-C10 alkyl, and the amino, hydroxy, carboxamido, alkyl, alkoxy, alkylcarbonyl, alkoxycarbonyl, alkylamino, dialkylamino, alkylaminoalkyl, and/or dialkylaminoalkyl may be substituted by one or two or more substituents selected from halogen, cyano, amino, nitro, C1-C10 alkyl, C1-C10 alkoxy, C1-C10 alkylcarbonyl, and/or C1-C10 alkoxycarbonyl, ##STR00026## wherein A.sub.1 to A.sub.4 are independently of one another CR or N, at least one of A.sub.1 to A.sub.4 is N, and R is hydrogen, amino, C1-C10 alkyl, C1-C10 alkoxy, C1-C10 alkylcarbonyl, C1-C10 alkoxycarbonyl, C1-C10 alkylamino, diC1-C10 alkylamino, C1-C10 alkylcarbonylamino, C1-C10 alkylaminoC1-C10 alkyl, or diC1-C10 alkylaminoC1-C10 alkyl, or two or more R's may be connected to each other to form a ring.

9. The carbon dioxide absorbing composition of claim 1, wherein the carbon dioxide absorbing composition further comprises water.

10. The carbon dioxide absorbing composition of claim 9, wherein the carbon dioxide absorbing composition further comprises one or more solvents other than water.

11. The carbon dioxide absorbing composition of claim 1, wherein the carbon dioxide absorbing composition has a carbon dioxide absorption equivalent represented by the following Equation 1 of 0.6 or more:
Carbon dioxide absorption equivalent=(moles of absorbed carbon dioxide)/(moles of ionic material in absorbing composition).[Equation 1]

12. The carbon dioxide absorbing composition of claim 1, wherein the carbon dioxide absorbing composition further comprises one or more amine absorbents.

13. The carbon dioxide absorbing composition of claim 12, wherein the carbon dioxide absorbing composition further comprises water.

14. The carbon dioxide absorbing composition of claim 13, wherein the carbon dioxide absorbing composition further comprises one or more solvents other than water.

15. A method of absorbing carbon dioxide comprising: reacting carbon dioxide and a phenolate-based anion and/or an imidazolate-based anion to respectively form a carbonate or a carbamate in an ionic material with a cyclic ammonium cation, thereby obtaining a carbon dioxide absorbing composition, and additionally physically absorbing carbon dioxide in the carbon dioxide absorbing composition comprising the ionic material.

16. The method of absorbing carbon dioxide of claim 15, wherein reacting carbon dioxide involves the cyclic ammonium cation to form the ionic material by following Reaction Formula 1 to form the carbonate and Reaction Formula 2 to form the carbamate, respectively, specified below:
CO.sub.2+[heterocycle-N.sup.+][phenolate-O.sup.].fwdarw.[heterocycle-N.sup.+][phenolate-OCO.sub.2.sup.][Reaction Formula 1]
CO.sub.2+[heterocycle-N.sup.+][imidazolate-N.sup.].fwdarw.[heterocycle-N.sup.+][imidazolate-NCO.sub.2.sup.],[Reaction Formula 2] wherein [heterocycle-N.sup.+] denotes the cyclic ammonium cation, [phenolate-O.sup.] denotes the phenolate-based anion, and [imidazolate-N.sup.] denotes the imidazolate-based anion.

17. A method of separating carbon dioxide, the method comprising: a first step of bringing the carbon dioxide absorbing composition of claim 1 into contact with a mixture comprising carbon dioxide; and a second step of heat treating the carbon dioxide absorbing composition to desorb carbon dioxide attached to the absorbing composition.

18. The method of separating carbon dioxide of claim 17, wherein the first step is performed under conditions of 20 to 80 C.

19. The method of separating carbon dioxide of claim 17, wherein the second step is performed under conditions of 70 to 150 C.

20. The method of separating carbon dioxide of claim 17, wherein when the first step and the second step are a unit process, carbon dioxide is continuously separated by repeating the unit process twice or more.

Description

DETAILED DESCRIPTION

[0057] Hereinafter, the present disclosure will be described in detail. Terms used in the present specification should be interpreted as having the meaning commonly understood by a person skilled in the art to which the present disclosure pertains, unless otherwise defined. Examples of the present specification are for a person skilled in the art to easily understand and carry out the present disclosure, descriptions which may obscure the gist of the present disclosure in the examples may be omitted, and the present disclosure is not limited by the examples.

[0058] The singular form used in the present specification may be intended to also include a plural form, unless otherwise indicated in the context. As used herein, the singular form of a, an, and the include plural referents unless the context clearly states otherwise.

[0059] In addition, the numerical range used in the present specification includes all values within the range including the lower limit and the upper limit, increments logically derived in a form and span of a defined range, all double limited values, and all possible combinations of the upper limit and the lower limit in the numerical range defined in different forms. Unless otherwise defined in the present specification, values which may be outside a numerical range due to experimental error or rounding off of a value are also included in the defined numerical range.

[0060] For the purposes of this specification, unless otherwise indicated, all numbers expressing quantities of ingredients, reaction conditions, dimensions, physical characteristics, and so forth used in the specification and claims are to be understood as being modified in all instances by the term about. Hereinafter, unless otherwise particularly defined in the present specification, about may be considered as a value within 30%, 25%, 20%, 15%, 10%, 5%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05% or 0.01 of a stated value. Unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are approximations that can vary depending upon the desired properties sought to be obtained by the present invention.

[0061] Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements.

[0062] In the present specification, the terms such as comprise, contain, have, and provided with mean that there is a characteristic or a constituent element described in the specification, and as long as it is not particularly limited, a possibility of adding one or more other characteristics or constituent elements is not excluded in advance.

[0063] The term single bond in the present specification refers to a case in which there is no atom in the corresponding area. For example, in a structure of XYZ, when Y is a single bond, X and Z is directly bonded to form a structure of XZ.

[0064] In some embodiments, there is provided a carbon dioxide absorbing composition comprising an ionic material comprising a cyclic ammonium cation represented by the following Chemical Formula 1:

##STR00006##

[0065] wherein [0066] L.sub.1 is a single bond, O, NR.sub.7, or (C1-C8)alkylene, [0067] R.sub.1 to R.sub.4 are each independently of one another hydrogen or (C1-C10)alkyl, and [0068] R.sub.5 to R.sub.7 are each independently of one another (C1-C20)alkyl or hydroxy(C1-C20)alkyl, or R.sub.5 and R.sub.7 may be bonded to each other to form a ring.

[0069] In some embodiments, the carbon dioxide absorbing composition is thermally and/or chemically stable, and when it is applied to a process, it has a low loss of the carbon dioxide absorbing composition by decomposition. In some embodiments, since the carbon dioxide absorbing composition with the ionic material is not easily decomposed in a desorption process under basic conditions at a high temperature, they may reduce periodic supplementation of the absorbing composition when they applied to the process, and thus, are economical.

[0070] Chemical stability at high temperature is particularly enhanced when the spiro ammonium cation is combined with a phenolate-based anion or an imidazolate-based anion to form the ionic material of the carbon dioxide absorbing composition.

[0071] An amine absorbent (e.g., monoethanolamine (MEA)) used in the conventional carbon dioxide absorbing composition has a benefit of a rapid reaction rate with carbon dioxide, but also has a problem of a high decomposition ratio after a carbon dioxide desorption process. However, when the carbon dioxide absorbing composition(s) according to the present disclosure comprises an ionic material comprising a cyclic ammonium cation having a specific structure and a phenolate-based anion and/or an imidazolate-based anion, it may decrease a decomposition ratio after the carbon dioxide desorption process as compared with a conventional amine absorbent.

[0072] Since the ionic material(s) of the present disclosure has lower corrosiveness than the conventional amine compound, a carbon dioxide absorbing composition comprising an ionic material at a high concentration may be prepared by using the ionic material, and the carbon dioxide absorbing composition may have significantly improved carbon dioxide absorption performance as compared with the conventional carbon dioxide absorbing composition including amine compounds.

[0073] In some embodiments, the cyclic ammonium cation of the present disclosure may be represented by the following Chemical Formula 2:

##STR00007##

[0074] wherein [0075] L.sub.1 is a single bond, O, NR.sub.7, or (C1-C5)alkylene, and [0076] R.sub.5 to R.sub.7 are each independently of one another (C1-C10)alkyl or hydroxy(C1-C10)alkyl, or R.sub.5 and R.sub.7 may be bonded to each other to form (C1-10)heterocycloalkyl.

[0077] In some embodiments, in Chemical Formula 2, L.sub.1 may be a single bond, O, NR.sub.7, or (C1-C3)alkylene, R.sub.5 and R.sub.6 each may be independently of each other (C1-C5)alkyl or hydroxy(C1-C5)alkyl, and R.sub.7 may be (C1-C5)alkyl.

[0078] In some embodiments, in Chemical Formula 2, L.sub.1 may be a single bond, O, NR.sub.7, or methylene, R.sub.5 and R.sub.6 may be independently of each other methyl, butyl, or hydroxy(C2-C3)alkyl, and R.sub.7 may be methyl.

[0079] In some embodiments, the cyclic ammonium cation of the present disclosure may be represented by the following Chemical Formula 3:

##STR00008##

[0080] wherein [0081] L.sub.2 is (C1-C10)alkylene, [0082] R.sub.1 to R.sub.4 are each independently of one another hydrogen or (C1-C5)alkyl, and

[0083] R.sub.6 is (C1-C10)alkyl or hydroxy(C1-C10)alkyl.

[0084] In some embodiments, in Chemical Formula 3, L.sub.2 may be (C1-C5)alkylene, R.sub.1 to R.sub.4 each may be independently of one another hydrogen or (C1-C3)alkyl, and R.sub.6 may be (C1-C5)alkyl or hydroxy(C1-C5)alkyl.

[0085] In some embodiments, in Chemical Formula 3, L.sub.2 may be ethylene, R.sub.1 to R.sub.4 may be hydrogen, and R.sub.6 may be butyl or propanol.

[0086] In some embodiments, in the carbon dioxide absorbing composition of the present disclosure, the ionic material may further comprise a phenolate-based anion represented by the following Chemical Formula 4 and/or an imidazolate-based anion represented by the following Chemical Formula 5:

##STR00009##

[0087] wherein [0088] R.sub.21 to R.sub.25 are each independently of one another hydrogen, amino, hydroxy, nitro, carboxamido, C1-C10 alkyl, C1-C10 alkoxy, C1-C10 alkylcarbonyl, C1-C10 alkoxycarbonyl, C1-C10 alkylamino, diC1-C10 alkylamino, C1-C10 alkylaminoC1-C10 alkyl, or diC1-C10 alkylaminoC1-C10 alkyl, and [0089] the amino, hydroxy, carboxamido, alkyl, alkoxy, alkylcarbonyl, alkoxycarbonyl, alkylamino, dialkylamino, alkylaminoalkyl, and dialkylaminoalkyl may be substituted by one or two or more substituents selected from halogen, cyano, amino, nitro, C1-C10 alkyl, C1-C10 alkoxy, C1-C10 alkylcarbonyl, and C1-C10 alkoxycarbonyl,

##STR00010##

[0090] wherein [0091] A.sub.1 to A.sub.4 are each independently of one another CR or N, [0092] at least one of A.sub.1 to A.sub.4 is N, and [0093] R is hydrogen, amino, C1-C10 alkyl, C1-C10 alkoxy, C1-C10 alkylcarbonyl, C1-C10 alkoxycarbonyl, C1-C10 alkylamino, diC1-C10 alkylamino, C1-C10 alkylcarbonylamino, C1-C10 alkylaminoC1-C10 alkyl, or diC1-C10 alkylaminoC1-C10 alkyl, or two or more R's may be connected to each other to form a ring.

[0094] In some embodiments, the carbon dioxide absorbing composition may comprise 20 to 80 wt %, or 25 to 77 wt %, or 30 to 75 wt % of the ionic material, based on the total weight of the composition.

[0095] In some embodiments, the carbon dioxide absorbing composition may further comprise water and/or one or more solvents other than water. The solvent other than water may be a nonaqueous solvent, and for example, may be one or more selected from ethylene glycol, propylene glycol, methyl glycol, methyl isopropyl carboxylate, methyl diethyl carboxylate, triethylene glycol, dimethyl sulfonate, and/or diethyl sulfonate, and may be ethylene glycol.

[0096] In some embodiments, the carbon dioxide absorbing composition may comprise 20 to 80 wt %, or 23 to 75 wt %, or 25 to 70 wt % of water, a solvent other than water, or a mixed solvent of water and a solvent other than water (such as a nonaqueous solvent).

[0097] In some embodiments, the carbon dioxide absorbing composition may have a carbon dioxide absorption equivalent represented by the following Equation 1 of 0.6 or more, or 0.6 to 3.0:

Carbon dioxide absorption equivalent=(moles of absorbed carbon dioxide)/(moles of ionic material in absorbing composition).[Equation 1]

[0098] In the carbon dioxide absorption mechanism of the ionic material comprising the cyclic ammonium cation and the phenolate-based anion and/or the imidazolate-based anion, a better carbon dioxide absorption equivalent may be shown by not only a chemical absorption method in which carbon dioxide and the phenolate-based anion and/or the imidazolate-based anion of the absorbing composition are reacted to form a carbonate and a carbamate represented by Reaction Formulae 1 and 2 but also a physical absorption method of trapping carbon dioxide in free volume of the carbon dioxide absorbing composition comprising the ionic material:

CO.sub.2+[heterocycle-N.sup.+][phenolate-O.sup.].fwdarw.[heterocycle-N.sup.+][phenolate-OCO.sub.2.sup.][Reaction Formula 1]

CO.sub.2+[heterocycle-N.sup.+][imidazolate-N.sup.].fwdarw.[heterocycle-N.sup.+][imidazolate-NCO.sub.2.sup.][Reaction Formula 2]

[0099] Accordingly, in some embodiments of the present disclosure, a new concept of carbon dioxide absorption is embodied by a method in which carbon dioxide and a phenolate-based anion and/or a imidazolate-based anion are reacted to form a carbonate and a carbamate of an absorbing composition in which carbon dioxide is chemically bound in an ionic material, and optionally in addition by a physical absorption method of trapping carbon dioxide in free volume of the carbon dioxide absorbing composition comprising the ionic material.

[0100] In some embodiments of this new concept of the present disclosure disclosed herein, the reaction of carbon dioxide involves the cyclic ammonium cation disclosed herein and follows the Reaction Formulae 1 and 2 specified herein.

[0101] In this new concept of the present disclosure too, chemical stability at high temperature is particularly enhanced when the cyclic ammonium cation is combined with a phenolate-based anion and/or an imidazolate-based anion to form the ionic material of the carbon dioxide absorbing composition.

[0102] In some embodiments of this new concept of the present disclosure, the carbon dioxide absorption composition is as defined herein.

[0103] The carbon dioxide absorbing composition comprising the ionic material may show a significantly improved effect on the absorption equivalent, as compared with a conventional carbon dioxide absorbing composition of amines, by the use of the cyclic ammonium cation material as disclosed herein and the phenolate-based anion and/or the imidazolate-based anion.

[0104] In some embodiments, the carbon dioxide absorbing composition may further comprise one or more amine absorbents, for example 1 to 5 or 1 to 3 amine absorbents. In some embodiments, the amine absorbent may be selected from monoethanolamine (MEA), N-methyldiethanolamine (MDEA), diethanolamine (DEA), triethanolamine (TEA), 2-amino-2-methyl-1-propanol (AMP), and/or piperazine (PZ).

[0105] In some embodiments, the carbon dioxide absorbing composition comprising the amine absorbent may further comprise water, and/or one or more solvents other than water in amounts as disclosed herein above.

[0106] In some embodiments, since the carbon dioxide absorbing composition comprising the ionic material has a low decrease rate of the carbon dioxide absorbing composition when it is stored for a long time at a heat treatment temperature for desorbing carbon dioxide which is attached to the absorbing composition, performance of the carbon dioxide absorbing composition may be maintained stable even after the carbon dioxide desorption process. The decrease rate of the carbon dioxide absorbing composition represented by the following Equation 2 may be 5% or less, or 4.5% or less, or 4% or less, 3% or less, 2% or less, 1.5% or less:

Decrease rate of carbon dioxide absorbing composition=100{(moles of ionic material after heat treatment)/(moles of ionic material before heat treatment)}100[Equation 2]

[0107] In some embodiments, a method of separating carbon dioxide using the carbon dioxide absorbing composition is provided. The method of separating carbon dioxide may comprise: a first step of bringing a carbon dioxide absorbing composition into contact with a mixture comprising carbon dioxide; and a second step of heat treating the carbon dioxide absorbing composition to desorb carbon dioxide attached to the absorbing composition.

[0108] In some embodiments, in the method of separating carbon dioxide, decomposition of the carbon dioxide absorbing composition is inhibited in the second step of desorbing carbon dioxide under basic conditions at a high temperature, thereby decreasing the decrease rate of the absorbing composition after desorbing carbon dioxide. Accordingly, the method of separating carbon dioxide has a small loss of the absorbing composition depending on the number of processes as compared with a method of absorbing carbon dioxide using the conventional carbon dioxide absorbing composition of amines, and thus, the amount of the absorbing composition which should be replenished after each process may be decreased and the process may be operated more economically.

[0109] In some embodiments, the first step of the method of separating carbon dioxide may be performed under the conditions of 20 to 80 C., or 25 C. to 65 C., or 30 C. to 50 C., but is not limited thereto.

[0110] In some embodiments, the second step of the method of separating carbon dioxide may be performed under the conditions of 70 to 150 C., or 80 C. to 140 C., or 90 C. to 130 C., but is not limited thereto.

[0111] In some embodiments, in the method of separating carbon dioxide according to the present disclosure, when the first step and the second step are a unit process, carbon dioxide may be continuously separated by repeating the unit process twice or more.

[0112] In some embodiments, the carbon dioxide absorbing composition according to the present disclosure is thermally and/or chemically stable, and/or has a low loss of the carbon dioxide absorbing composition by decomposition. Therefore, in some embodiments, in the method of separating carbon dioxide using the carbon dioxide absorbing composition, atmospheric emissions of by-products by decomposition of the absorbing composition are low for the reason described above, and may be a very environmentally friendly method.

[0113] In some embodiments, the method of separating carbon dioxide using the carbon dioxide absorbing composition has a low decomposition rate of the carbon dioxide absorbing composition after a carbon dioxide desorption process, and thus, allows repeated use of the absorbing composition and is a very economical method.

[0114] In some embodiments, a method of capturing carbon dioxide is provided, comprising contacting carbon dioxide with a carbon dioxide absorbing composition comprising an ionic material comprising a cyclic ammonium cation represented by the following Chemical Formula 1:

##STR00011##

[0115] wherein [0116] L.sub.1 is a single bond, O, NR.sub.7, or (C1-C8)alkylene, [0117] R.sub.1 to R.sub.4 are each independently of one another hydrogen or (C1-C10)alkyl, and [0118] R.sub.5 to R.sub.7 are each independently of one another (C1-C20)alkyl or hydroxy(C1-C20)alkyl, or R.sub.5 and R.sub.7 may be bonded to each other to form a ring whereby the carbon dioxide absorbing composition captures the carbon dioxide.

[0119] In some embodiments, a method of reducing greenhouse gas emissions comprising carbon dioxide is provided, comprising: contacting the greenhouse gas emissions with a carbon dioxide absorbing composition comprising an ionic material comprising a cyclic ammonium cation represented by the following Chemical Formula 1:

##STR00012##

[0120] wherein [0121] L.sub.1 is a single bond, O, NR.sub.7, or (C1-C8)alkylene, [0122] R.sub.1 to R.sub.4 are each independently of one another hydrogen or (C1-C10)alkyl, and [0123] R.sub.5 to R.sub.7 are each independently of one another (C1-C20)alkyl or hydroxy(C1-C20)alkyl, or R.sub.5 and R.sub.7 may be bonded to each other to form a ring whereby the carbon dioxide absorbing composition captures carbon dioxide from the greenhouse gas emissions.

[0124] Hereinafter, some embodiments of the carbon dioxide absorbing composition comprising the ionic material comprising the cyclic ammonium cation and the method of separating carbon dioxide using the same will be described in more detail by the specific examples.

[Preparation Example 1] Preparation of Ionic Material IC-1

[0125] 40 mmol of a chloride compound or a cyclic ammonium cation shown in IC-1 of the following Table 1 and 40 mmol of a sodium compound of a phenolate anion also shown in IC-1 of the following Table 1 were added, 40 mL of ethanol was added, and stirring was performed at room temperature for 2 hours. The produced sodium chloride solid was removed by filtration, and drying under vacuum was performed at 50 C. for 15 hours to obtain an ionic material IC-1. The obtained ionic material IC-1 was measured by NMR, and the results are shown in Table 1.

[Preparation Examples 2 to 8] Preparation of Ionic Materials IC-2 to IC-8

[0126] Ionic materials IC-2 to IC-8 were prepared in the same manner as in Preparation Example 1, except that the chloride compounds of cyclic ammonium cations shown in IC-2 to IC-8 of the following Table 1 and the sodium compound of phenolate anions or an imidazolate anion also shown in IC-2 to IC-8 of the following Table 1 were used instead of the chloride cation compound and the anion sodium compound used in Preparation Example 1. The obtained ionic materials were measured by NMR, and the results are shown in Table 1.

TABLE-US-00001 TABLE 1 Ionic material NMR results Preparation Example 1 [00013] .sup.1H NMR (500 MHz), D.sub.2O, 25 C.: = 7.14 (t, 2H), 6.60 (m, 3H), 3.99 (t, 2H), 3.43 (t, 2H), 3.37 (m, 2H), 3.30 (m, 2H), 3.05 (s, 3H), 1.83 (m, 4H), 1.61 (m, 2H) Preparation Example 2 [00014] .sup.1H NMR (500 MHz), D.sub.2O, 25 C.: = 7.15 (t, 2H), 6.61 (m, 3H), 3.98 (t, 4H), 3.56 (t, 4H), 3.43 (t, 4H), 1.85 (m, 4H), 1.64 (m, 2H) Preparation Example 3 [00015] .sup.1H NMR (500 MHz), D.sub.2O, 25 C.: = 7.18 (t, 2H), 6.67 (m, 3H), 4.01 (t, 4H), 3.42 (m, 6H), 3.10 (t, 3H), 1.37 (t, 3H) Preparation Example 4 [00016] .sup.1H NMR (500 MHz), D.sub.2O, 25 C.: = 7.18 (t, 2H), 6.68 (m, 3H), 3.99 (t, 4H), 3.42 (m, 6H), 3.11 (s, 3H), 1.74 (m, 2H), 1.38 (m, 2H), 0.97 (m, 3H) Preparation Example 5 [00017] .sup.1H NMR (500 MHz), D.sub.2O, 25 C.: = 7.01 (t, 2H), 6.49 (d, 2H), 6.43 (t, 1H), 3.50 (m, 2H), 3.15 (m, 8H), 3.12 (m, 6H), 1.93 (m, 2H) Preparation Example 6 [00018] .sup.1H NMR (500 MHz), D.sub.2O, 25 C.: = 6.90 (t, 2H), 6.42 (d, 2H), 6.33 (t, 1H), 3.80 (m, 2H), 3.29 (m, 4H), 3.23 (m, 2H), 2.92 (s, 3H), 2.59 (m, 4H), 2.15 (s, 3H) Preparation Example 7 [00019] .sup.1H NMR (500 MHz), D.sub.2O, 25 C.: = 6.95 (t, 2H), 6.45 (d, 2H), 6.39 (t, 1H), 3.16 (m, 6H), 2.92 (s, 3H), 2.61 (m, 4H), 2.17 (s, 3H), 1.51 (m, 2H), 1.20 (m, 2H), 0.80 (t, 3H) Preparation Example 8 [00020] .sup.1H NMR (500 MHz), D.sub.2O, 25 C.: = 7.61 (s, 1H), 7.00 (s, 2H), 3.87 (t, 2H), 3.27 (m, 4H), 3.19 (m, 2H), 2.96 (s, 3H), 1.74 (m, 4H), 1.52 (m, 2H)

Examples 1 to 10

[0127] The carbon dioxide absorbing compositions of Examples 1 to 10 including the ionic materials of Preparation Examples 1 to 8 and solvents having the compositions of Table 2 were prepared.

[0128] The ionic material and the solvent were added according to wt % regardless of the addition order, and mixing was performed at 20 to 40 C. for 5 to 60 minutes to prepare the carbon dioxide absorbing compositions of Examples 1 to 10.

TABLE-US-00002 TABLE 2 Ionic material (wt %) Solvent (wt %) Example Preparation Example 1 (IC-1) Water (70%) 1 (30%) Example Preparation Example 2 (IC-2) Water (70%) 2 (30%) Example Preparation Example 3 (IC-3) Water (70%) 3 (30%) Example Preparation Example 4 (IC-4) Water (70%) 4 (30%) Example Preparation Example 5 (IC-5) Water (70%) 5 (30%) Example Preparation Example 6 (IC-6) Water (70%) 6 (30%) Example Preparation Example 7 (IC-7) Water (70%) 7 (30%) Example Preparation Example 8 (IC-8) Water (70%) 8 (30%) Example Preparation Example 1 (IC-1) Water (45%), 9 (45%) ethylene glycol (10%) Example Preparation Example 8 (IC-8) Water (45%), 10 (45%) ethylene glycol (10%)

[Comparative Example 1] Preparation of Carbon Dioxide Absorbing Composition

[0129] The carbon dioxide absorbing composition of Comparative Example 1 including amine and a solvent was prepared with the composition of the following Table 3.

[0130] The amine and the solvent were added according to the weight ratio regardless of the addition order, and mixing was performed at 20 to 40 C. for 5 to 60 minutes to prepare the carbon dioxide absorbing composition of Comparative Example 1.

TABLE-US-00003 TABLE 3 Amine (wt %) Solvent (wt %) Comparative Example 1 [00021] Water (70%) (30%)

[Experimental Example 1] Evaluation of Carbon Dioxide Absorption Performance

[0131] In order to evaluate the carbon dioxide absorption performance of the carbon dioxide absorbing compositions according to Examples 1 to 8 and Comparative Example 1, the carbon dioxide absorption performance was measured using a vapor liquid equilibrium (VLE) apparatus manufactured according to a reference (Applied Chemistry for Engineering, 2010, 21(3), 284-290). As the vapor liquid equilibrium apparatus, an apparatus including a cylinder for storing carbon dioxide (150 mL), a constant temperature water bath, a stainless steel reactor equipped with a thermometer (73 mL), an electronic pressure gauge, and an agitator was used. At this time, absorption ability was measured by maintaining a constant temperature of 40 C. in the cylinder and the reactor using a constant temperature water bath and a heating block, respectively. A measurement error range of the reactor was 0.1 C. and 0.01 bar.

[0132] Evaluation of carbon dioxide absorption performance was performed specifically by the following method. First, the insides of a cylinder for storing carbon dioxide and an absorption reactor were sufficiently replaced with nitrogen, and the cylinder for storing carbon dioxide was filled with carbon dioxide and maintained at 40 C. under 1 bar. Next, the carbon dioxide absorbing compositions (6.0 g) of Examples 1 to 8 and Comparative Example 1 were added into the reactor, which was maintained at 40 C., a valve connecting the cylinder and the reactor was opened, and a pressure was measured after reaching absorption equilibrium. An equilibrium pressure was measured every 30 minutes, and the process was repeated until there was no change in pressure between the cylinder and the reactor.

[0133] An ideal gas equation was used to calculate the number of moles of absorbed carbon dioxide depending on pressure change. The number of moles of the absorbed carbon dioxide was used to analyze the carbon dioxide absorption equivalent calculated by the following Equation 3, which is shown in the following Table 4:

Carbon dioxide absorption equivalent=(moles of absorbed carbon dioxide)/(moles of ionic material in absorbing composition)[Equation 3]

TABLE-US-00004 TABLE 4 Carbon dioxide absorption equivalent (mol/mol) Example 1 1.06 Example 2 0.85 Example 3 1.03 Example 4 1.01 Example 5 0.81 Example 6 0.61 Example 7 0.64 Example 8 0.94 Comparative Example 1 0.59

[Experimental Example 2] Thermal Stability Evaluation

[0134] In order to evaluate the thermal stability of the carbon dioxide absorbing compositions according to Examples 9 and 10 and Comparative Example 1, carbon dioxide was bubbled into the absorbing compositions for 30 minutes or more at a speed of 100 cc/min to sufficiently absorb carbon dioxide. 10.0 g of the composition to which carbon dioxide was absorbed was added to a stainless steel container (50 mL), which was heat treated by being stored in an oven maintained at a constant temperature of 130 C. for 4.5 days, and the decrease rate of the carbon dioxide absorbing composition calculated by the following Equation 4 is shown in the following Table 5:

Decrease rate of carbon dioxide absorbing composition=100{(moles of ionic material after heat treatment)/(moles of ionic material before heat treatment)}100[Equation 4]

TABLE-US-00005 TABLE 5 Average decrease rate (%) Example 9 3.5 Example 10 3.7 Comparative Example 1 5.4

[0135] As shown in Table 4, it was found that the carbon dioxide absorption equivalents of the examples were all 0.6 or more, which showed improved carbon dioxide absorption performance as compared with the comparative example.

[0136] In addition, as shown in Table 5, it was found that the decrease rate of the ionic material of the Examples 9 and 10 was 4.0% or less, and the compositions had excellent stability at a high temperature. However, the comparative example to which monoethanolamine which is widely used as a carbon dioxide absorbing composition of amines was introduced showed a higher decrease rate than Examples 9 and 10, and it was found from the results that the Examples of the present disclosure showed significantly improved stability in the carbon dioxide absorption process.

[0137] Since the carbon dioxide absorbing composition comprising the ionic material comprising the cyclic ammonium cation and the phenolate-based anion or the imidazolate-based anion according to the present disclosure had improved stability under the basic environment at a high temperature, the problems of desorption and reuse restriction occurring in the conventional carbon dioxide absorbing composition using monoethanolamine were improved and it was very easy to apply a process for mass production.

[0138] In addition, the method of separating carbon dioxide using the carbon dioxide absorbing compositions of Examples 9 and 10 were more effective for desorption of carbon dioxide than a method using the carbon dioxide absorbing composition of amines, and was a very economical method since it allowed repeated use of the carbon dioxide absorbing composition.

[0139] The carbon dioxide absorbing composition according to the present disclosure is thermally and/or chemically stable to reduce atmospheric emissions of decomposition products when it is applied to a process, and/or has thermal stability since it is not easily decomposed even under basic conditions at high temperature as compared with a conventional carbon dioxide absorbing composition of amines.

[0140] In addition, since the carbon dioxide absorbing composition according to the present disclosure can have low corrosiveness as compared with the conventional carbon dioxide absorbing composition of amines, a carbon dioxide absorbing composition including an ionic material at a high concentration may be prepared, whereby significantly improved absorption performance may be shown. In addition, the carbon dioxide absorbing composition of the present disclosure can allow easy desorption of carbon dioxide even with low renewable energy and is very effective for absorbing and desorbing carbon dioxide, as compared with the conventional carbon dioxide absorbing composition of amines.

[0141] The method of separating carbon dioxide using the carbon dioxide absorbing composition according to the present disclosure can allow improved absorption performance and/or stable process operation, and thus, may be easily industrially applied in a very economical and environmentally friendly manner.

[0142] Hereinabove, although the present disclosure has been described by specific matters, and limited examples and comparative example, they have been provided only for assisting the entire understanding of the present disclosure, and the present disclosure is not limited to the implementations, and various modifications and changes may be made by those skilled in the art to which the present disclosure pertains from the description.

[0143] Therefore, the present disclosure should not be limited to the above-described exemplary embodiments in keeping with the scope and spirit of the disclosure.