USE OF CARBOXYLATE COMPOUND AS ABSORBENT FOR CAPTURING CARBON DIOXIDE

Abstract

Provided is the use of a carboxylate compound as an absorbent for capturing carbon dioxide and/or in the preparation of an absorbent for capturing carbon dioxide. In the carboxylate compound, the carboxylate anion is a carboxylate radical with a carbon chain having a carbon atom number of more than 3, or a branched-chain carboxylate radical having a carbon atom number of more than 6; and the cation is a substituted quaternary ammonium ion, quaternary phosphorus ion, pyridinium ion, pyrrolium ion, piperidinium ion, imidazolium ion or metal ion. In the present invention, a method which can capture carbon dioxide in an efficient and energy-saving manner by using a carboxylate compound and has water stability is involved, and the method comprises the following step: putting an aqueous solution of a carboxylate compound in a carbon dioxide atmosphere to absorb carbon dioxide, thereby obtaining a carboxylate and carbon dioxide conjugate precipitated from water.

Claims

1-7. (canceled)

8. A method for capturing carbon dioxide, comprises using a carboxylate compound as an absorbent, wherein, in the carboxylate compound, the carboxylate acid anion is a carboxylate radical with a branched chain having a total carbon atom number of more than 6, and the cation is selected from at least one of a substituted quaternary ammonium ion, quaternary phosphorus ion, pyridinium ion, pyrrole ion, piperidinium ion, imidazolium ion and metal ion; wherein, the structural formulas of the substituted quaternary ammonium ion and the substituted quaternary phosphine ion are shown in the following formulas I-1 and II-1: ##STR00009## ##STR00010## in formulas I-1 and formula II-1, n is 1-4 and m is 1-16, and the substituents in formula I-1 and formula II-1 are the same or different.

9. The method of claim 8, wherein, the carboxylate radical with a branched chain having a total carbon atom number of more than 6 has a carbon atom number of 7-20.

10. The method of claim 8, wherein, the carboxylate radical with a branched chain having a total carbon atom number of more than 6 has a carbon atom number of 8-16.

11. The method of claim 8, wherein, the carboxylate radical with a branched chain having a total carbon atom number of more than 6 is selected from at least one of 2,2-dimethylhexanoate, 2-ethylhexanoate, 2-ethylheptanoate, 2-propylpentanoate, 2-propylhexanoate, 2-propylnonanoate, 2-butyloctanoate and 2-hexyldecanoate.

12. The method of claim 8, wherein, the substituted quaternary ammonium ion is selected from at least one of tetramethyl ammonium, tetraethyl ammonium, tributylmethyl ammonium, triethylbutylammonium, tetrabutylammonium and tributylhexyl ammonium; and the substituted quaternary phosphorus ion is selected from at least one of tetramethyl phosphine, tetraethyl phosphine and tributylmethyl phosphine, tetrabutyl phosphine, tributylhexyl phosphine, tributyloctyl phosphine, tributyldecadecyl phosphine, tributyldodecyl phosphine, tributyltetradecyl phosphine, and tributylhexadecyl phosphine.

13. The method of claim 8, wherein, the pyridinium ion is N-substituted pyridinium cation, and its structure formula is shown in the following formula III; the pyrrolidinum ion is N-substituted pyrrole cation, and its structure formula is shown in the following formula IV; the piperidinium ion is N-substituted piperidinium cation, and its structure formula is shown in the following formula V; the imidazolium ion is a disubstituted or/and trisubstituted imidazolium cation, and its structure formula is shown in the following formula VI; and the metal ion is selected from at least one of lithium, sodium, potassium and cesium; ##STR00011## ##STR00012## ##STR00013## ##STR00014## in formulas III, IV, V and VI, R.sub.1 and R.sub.2 are straight aliphatic chains with carbon atoms greater than or equal to 1, R.sub.3 is H or CH.sub.3, and R.sub.1 and R.sub.2 are the same or different.

14. The method of claim 13, wherein, R.sub.1 and R.sub.2 in the formula III, IV, V and VI are straight aliphatic chains with 1-10 carbon atoms.

15. A method of capturing carbon dioxide in an efficient and energy-saving manner using carboxylate compounds that are stable to water, comprising the following steps of: placing the aqueous solution of the carboxylate compound in carbon dioxide atmosphere to absorb carbon dioxide.

16. The method of claim 15, wherein, a molar ratio of the carboxylate compound and water is 1:0.5-300, and a condition for absorbing carbon dioxide is as follows: the partial pressure of carbon dioxide is 0.01-2 MPa; specifically 0.01 MPa, 0.1 MPa, 2 MPa; the temperature is 25-80° C., specifically 25° C. and 80° C.

17. The method of claim 15, wherein, the molar ratio of the carboxylate compound to water is 1:0.5-100; and the conditions for absorbing carbon dioxide are as follows: the partial pressure of carbon dioxide is 0.00004-0.5 MPa; and the temperature is 5-80° C.

18. The method of claim 15, wherein, carbon dioxide absorption amount per mole of the carboxylate compound is 0.1-1.2 moles.

19. The method of claim 15, wherein, the carbon dioxide absorption amount per mole of the carboxylate compound is 0.1-1.1 moles.

20. The method of claim 15, wherein the method further comprises the step of regeneration of the carboxylate compound after absorbing carbon dioxide.

21. The method of claim 20, wherein, the regeneration has the following steps of: under reduced pressure, the pressure is 0.01-1 atmosphere, the temperature is 10-120° C., and the time is 1 min-10 h.

22. A method for preparation of an absorbent for capturing carbon dioxide, comprises using carboxylate compound as raw material, wherein, in the carboxylate compound, the carboxylate acid anion is a carboxylate radical with a branched chain having a total carbon atom number of more than 6, and the cation is selected from at least one of a substituted quaternary ammonium ion, quaternary phosphorus ion, pyridinium ion, pyrrole ion, piperidinium ion, imidazolium ion and metal ion; wherein, the structural formulas of the substituted quaternary ammonium ion and the substituted quaternary phosphine ion are shown in the following formulas I-1 and II-1: ##STR00015## ##STR00016## in formulas I-1 and formula II-1, n is 1-4 and m is 1-16, and the substituents in formula I-1 and formula II-1 are the same or different.

23. The method of claim 22, wherein the carboxylate radical with a branched chain having a total carbon atom number of more than 6 has a carbon atom number of 7-20.

24. The method of claim 22, wherein the carboxylate radical with a branched chain having a total carbon atom number of more than 6 has a carbon atom number of 8-16.

25. The method of claim 22, wherein the carboxylate radical with a branched chain having a total carbon atom number of more than 6 is selected from at least one of 2,2-dimethylhexanoate, 2-ethylhexanoate, 2-ethylheptanoate, 2-propylpentanoate, 2-propylhexanoate, 2-propylnonanoate, 2-butyloctanoate and 2-hexyldecanoate.

26. The method of claim 22, wherein the substituted quaternary ammonium ion is selected from at least one of tetramethyl ammonium, tetraethyl ammonium and tributylmethyl ammonium triethylbutylammonium, tetrabutylammonium and tributylhexyl ammonium; and the substituted quaternary phosphorus ion is selected from at least one of tetramethyl phosphine, tetraethyl phosphine and tributylmethyl phosphine, tetrabutyl phosphine, tributylhexyl phosphine, tributyloctyl phosphine, tributyldecadecyl phosphine, tributyldodecyl phosphine, tributyltetradecyl phosphine, and tributylhexadecyl phosphine.

27. The method of claim 22, wherein the pyridinium ion is N-substituted pyridinium cation, and its structure formula is shown in the following formula III; the pyrrolidinum ion is N-substituted pyrrole cation, and its structure formula is shown in the following formula IV; the piperidinium ion is N-substituted piperidinium cation, and its structure formula is shown in the following formula V; the imidazolium ion is a disubstituted or/and trisubstituted imidazolium cation, and its structure formula is shown in the following formula VI; and the metal ion is selected from at least one of lithium, sodium, potassium and cesium; ##STR00017## ##STR00018## ##STR00019## ##STR00020## in formulas III, IV, V and VI, R.sub.1 and R.sub.2 are straight aliphatic chains with carbon atoms greater than or equal to 1, R.sub.3 is H or CH.sub.3, and R.sub.1 and R.sub.2 are the same or different.

Description

DETAILED DESCRIPTION

[0046] The experimental methods in the following embodiments are conventional methods unless otherwise specified.

[0047] Carboxylate salts in the following embodiment are synthesized by a mature technique (Suarez, P. A. Z.; Dullius, J. E. L.; Einloft, S.; DE Souza R. F. and Dupont, J., Polyhedron, 1996, 15, 1217-1219).

[0048] The embodiments described below are only used to explain the present application and should not be construed as limiting the scope of use of the present invention.

Example 1

[0049] 2 mmol of tributylhexyl phosphine 2-ethylhexanoate (0.86 g) and 40 mmol of water (0.72 g) were added in a glass bottle, a carbon dioxide balloon was connected to make the solution in carbon dioxide at one atmosphere. After stirring at 25° C. for 12 hours, the system was divided into an organic phase and an aqueous phase. The balloon was taken off and the gas carbon dioxide on the upper part of the solution in the bottle was replaced with air, then titrated with sodium hydroxide solution (0.2 w%), phenolphthalein was used as the indicator, and the carbon dioxide absorption amount was 0.98 mmol.

[0050] Under the same conditions, tributylhexyl phosphine 2-ethylhexanoate can be replaced with the following reagents, and the absorption of carbon dioxide by tetrabutyl phosphine 2-ethylhexanoate, tributyloctyl phosphine 2-ethylhexanoate, tributyldecadecyl phosphine 2-ethylhexanoate, tributyldodecyl phosphine 2-ethylhexanoate, tributyltetradecyl phosphine 2-ethylhexanoate, tributylhexadecyl phosphine 2-ethylhexanoate, tetrabutylammonium 2-ethylhexanoate, triethylbutylammonium 2-ethylhexanoate, tributylhexyl ammonium 2-ethylhexanoate, tributylhexyl phosphine 2,2-dimethylbutyrate, tributylhexyl phosphine 2-propylpentanoate, tributylhexyl phosphine 2,2-dimethylhexanoate, tributylhexyl phosphine 2-propylhexanoate, tributylhexyl phosphine 2-ethylheptanoate, tributylhexyl phosphine cyclohexyl formate and tributylhexyl phosphine n-octanoate with 2 mmol of each (to which 40 mmol of water was added respectively) was measured respectively. After absorbing carbon dioxide, a new liquid phase or solid phase was formed respectively, and the absorption amounts were 0.87, 2.2, 1.8, 1.6, 1.6, 1.7, 0.86, 0.24, 0.96, 0.22, 1.02, 0.53, 1.0, 0.99, 0.71 and 0.36 mmol, respectively.

Example 2

[0051] Substantially the same as Example 1 of the present invention, except that 2 mmol of tributylhexyl phosphine 2-ethylhexanoate (0.86 g) and 1 mmol of water were added, the others were completely the same as Example 1, and the carbon dioxide absorption amount was 1.0 mmol. It showed that the absorption amount when the molar ratio of the carboxylate compound to water was 1:0.5 was compared with that of Example 1, its carbon dioxide absorption amount was stable to water.

Example 3

[0052] Substantially the same as Example 2 of the present invention, except that 2 mmol of water, the others were completely the same as Example 2, and the carbon dioxide absorption amount was 1.0 mmol. It showed that the absorption amount when the molar ratio of the carboxylate compound and water was 1: 1 was compared with that of Example 1, its carbon dioxide absorption amount was stable to water and does not change with the increase of water.

Example 4

[0053] Substantially the same as Example 1 of the present invention, for tributylhexyl phosphine 2-ethylhexanoate, except that the temperature was at 80° C., the others were completely the same as Example 1. After absorbing carbon dioxide, a new organic phase was formed, and its carbon dioxide absorption amount was 0.62 mmol. It showed that the absorption amount when the above carboxylate solution was at different temperatures was compared with that of Example 1 of the present invention, a higher carbon dioxide capture capacity can be still obtained at high temperatures.

Example 5

[0054] Substantially the same as Example 1 of the present invention, for tributylhexyl phosphine 2-ethylhexanoate, except that the atmosphere was 0.01 MPa of carbon dioxide partial pressure and 0.09 MPa of nitrogen, the others were completely the same as Example 1, and the carbon dioxide absorption amount was 0.40 mmol. It showed that the absorption amount when the above carboxylate solution was at low partial pressure of carbon dioxide was compared with that of Example 1 of the present invention, a higher carbon dioxide capture capacity can be still obtained at low carbon dioxide partial pressure.

Example 6

[0055] 2 mmol of trityloctyl phosphine 2-ethylhexanoate (0.92 g), 40 mmol of water (0.72 g) were added into a pressure kettle, 2 MPa of carbon dioxide was introduced, and stirred at 25° C. for 12 hours. After decompression, after replacing the gas carbon dioxide on the upper part of the solution in the kettle with air, titrated with sodium hydroxide solution (0.2 w%) using phenolphthalein as the indicator, the carbon dioxide absorption amount was 1.2 mmol. It showed that the absorption amount when the above carboxylate solution was at high carbon dioxide pressure was compared with that of Example 1 of the present invention, a higher carbon dioxide capture capacity can be still obtained at high carbon dioxide partial pressure .

Example 7

[0056] Substantially the same as Example 1 of the invention, for tributylhexyl phosphine 2-ethylhexanoate, except that the carbon dioxide atmosphere was changed to carbon dioxide bubbling (20 ml/min) and absorbed for 30 minutes, the others were completely the same as Example 1, and the carbon dioxide absorption amount was 0.98 mmol. From the comparison of Examples 1 and 7, it can be seen that different absorption modes had relatively small effect on the carbon dioxide absorption amount, indicating that the carbon dioxide absorption amount of the present invention was not affected by the absorption modes.

Example 8

[0057] For tributylhexyl phosphine 2-ethylhexanoate, the carbon dioxide absorption part was completely the same as in Example 1 of the present invention. After the absorption was completed, it was exposed to the air and stirred for 3 hours at room temperature (25° C.). It was determined that carbon dioxide was released completely. It showed that the above-mentioned carboxylate solution can be regenerated after absorbing carbon dioxide.

Example 9

[0058] Substantially the same as Example 8 of the present invention, except that the release part was stirred at 80° C. for 30 minutes, the others were completely the same as Example 8. It was determined that carbon dioxide was released completely. From the comparison of Example 8 and Example 9 of the present invention, it can be seen that carboxylate compounds can be regenerated at different temperatures.

Example 10

[0059] Substantially the same as Example 8 of the invention, except that the release part was changed to keep stirring for 1 hour under reduced pressure of the water pump (0.01 atmosphere), the others are completely the same as Example 8. It was determined that carbon dioxide was released completely.. From the comparison of Example 8 and Example 10 of the present invention, it can be seen that the regeneration of carboxylate compounds can be achieved under different pressures.

Example 11

[0060] 1 mmol of tributylhexadecyl phosphine 2-ethylhexanoate (57 mg) was added into 5.4 g of water (0.3 mol). After dissolution, carbon dioxide bubbles (20 ml/min) were bubbled into the solution at room temperature for three minutes, and the solution became turbid, indicating that the carboxylate could effectively absorb carbon dioxide at this concentration and precipitate after absorption. Stop introducing carbon dioxide, expose the solution to the air, continue stir at room temperature (25° C.), and the solution become clear after 3 minutes, indicating that the solution can release carbon dioxide quickly. From comparison of Example 1 and Example 11 of the present invention, it can be seen that the absorption and regeneration of carboxylate compounds can be achieved at different concentrations and different absorption modes.

Example 12

[0061] 2 mmol of tetrabutylammonium 2-ethylhexanoate (0.434 g) and 2 mmol of water (0.036 g) were added in a glass bottle, a carbon dioxide balloon was connected to make the solution in carbon dioxide at 0.1 MPa. After stirring at 25° C. for 12 hours, the system was divided into an organic phase and an aqueous phase. The balloon was taken off and the gas carbon dioxide on the upper part of the solution in the bottle was replaced with air, then titrated with sodium hydroxide solution (0.2 w%), phenolphthalein was used as the indicator, and the carbon dioxide absorption amount was 1.0 mmol.

[0062] Under the same conditions, tetramethyl ammonium 2-ethylhexanoate can be replaced with the following reagents, and the absorption of carbon dioxide by tetraethyl ammonium 2-ethylhexanoate, tetramethyl phosphine 2-ethylhexanoate, tetramethyl ammonium 2-ethylhexanoate, tetraethyl ammonium 2-ethylhexanoate, tributylmethyl phosphine 2-ethylhexanoate, tributylmethyl phosphine 2,2-dimethylhexanoate, tributylmethyl phosphine 2-ethylheptanoate, tributylmethyl phosphine 2-propylpentanoate, tributylmethyl phosphine 2-propylhexanoate, tetramethyl ammonium 2-propylnonanoate, tetramethyl ammonium 2-butyloctanoate, tetramethyl ammonium 2-hexyldecanoate, sodium 2-ethylhexanoate, potassium 2,2-dimethylhexanoate, lithium 2-ethylheptanoate, cesium 2-propylpentanoate, N-butylpiperidinium 2-ethylhexanoate, N-butyl-N-methylpyrrolidinum 2-ethylhexanoate, N-butyl-N-methylpiperidinium2-ethylhexanoate and 1-butyl -2,3-dimethyl 2-ethylhexanoate with 2 mmol of each (to which 2 mmol of water was added respectively) was measured respectively. After absorbing carbon dioxide, a new liquid phase or solid phase was formed respectively, and the absorption amounts were 1.03, 0.99, 1.02, 0.98, 1.03, 1.01, 0.99, 1.00, 1.01, 1.01, 1.01, 1.01, 1.01, 1.03, 1.05, 0.99, 0.97, 0.98, 0.95, 1.00, 1.02, 0.99, 1.02 mmol, respectively. All absorptions were in the range of 0.95-1.05 mmol.

[0063] It indicated that all above substances can effectively absorb carbon dioxide.

Example 13

[0064] Substantially the same as Example 12 of the present invention, except that 2 mmol of tributylmethyl ammonium 2-ethylhexanoate (0.86 g) and 1 mmol of water (0.018 g) were added, the others were completely the same as Example 12, and the carbon dioxide absorption amount was 1.0 mmol. It showed that the absorption amount when the molar ratio of the carboxylate compound to water was 1:0.5 was compared with that of Example 12, its carbon dioxide absorption amount was stable to water within a certain range.

Example 14

[0065] Substantially the same as Example 12 of the present invention, except that 2 mmol of sodium 2-hexyldecanoate (0.56 g) was added into 200 mmol of water (3.6 g of water), the others were completely the same as Example 12, and the carbon dioxide absorption amount was 2.05 mmol. It showed that the carbon dioxide absorption amount of the above-mentioned carboxylates was stable to water in a large range.

[0066] After absorption, the solution was heated at 120° C. for 3 hours, and it was determined that carbon dioxide was released completely. It indicated that the carboxylate solution can be regenerated after absorbing carbon dioxide.

Example 15

[0067] Substantially the same as Example 14 of the present invention, except that the absorption temperature was 80° C., the others are completely the same as Example 3, and the carbon dioxide absorption amount was 2.0 mmol. It showed that the carbon dioxide absorption amount of the above-mentioned carboxylates was stable to temperature in a large range compared with that of Example 14.

Example 16

[0068] 2 mmol of tetramethyl ammonium 2-ethylhexanoate (0.69 g) and 0.7 g of water were added in a glass bottle, a carbon dioxide balloon was connected to make the solution in carbon dioxide at one atmosphere, stirred at 5° C. for 12 hours. The balloon was taken off and the gas carbon dioxide on the upper part of the solution in the bottle was replaced with air, then titrated with sodium hydroxide solution (0.2 w%), phenolphthalein was used as the indicator, the carbon dioxide absorption amount was 1.2 mmol. Compared with Example 12, it was shown that reducing the absorption temperature was beneficial to improving the absorption.

[0069] After absorption, the solution was exposed to air and stirred continuously at room temperature (25° C.) for 3 hours, and it was determined that carbon dioxide was released completely. This shows that the above carboxylate solution can be regenerated after absorbing carbon dioxide.

Example 17

[0070] Substantially the same as Example 12 of the present invention, for tetrabutylammonium 2-ethylhexanoate, except that the partial pressure of carbon dioxide was 0.01 MPa and nitrogen 0.09 MPa, the others are the same as Example 12, and the carbon dioxide absorption amount was 0.98 mmol.

[0071] 0.278 g of sodium 2-hexyldecanoate (1 mmol) was dissolved in 1 g of water, and the air pump was used to provide air for bubbling (the partial pressure of carbon dioxide in the atmosphere was about 0.00004 MPa). The air flow was 10 ml per minute, after 12 hours, titrated with sodium hydroxide solution (0.2 w%) until it was clear, and the carbon dioxide absorption amountwas 0.10 mmol.

[0072] The carbon dioxide absorption amount by the above carboxylate solution at low partial pressure of carbon dioxide was compared with that of Example 12 of the present invention, indicating that a high carbon dioxide capture capacity can still be obtained at low partial pressure of carbon dioxide, and even a certain amount of carbon dioxide can be absorbed from the atmosphere.

Example 18

[0073] 2 mmol of tributylmethyl ammonium 2-ethylhexanoate (0.69 g), 2 mmol of water (0.036 g) were added to the pressure kettle, 0.5 MPa carbon dioxide was introduced, and the mixture was stirred at 25° C. for 12 hours. After decompression, the gas carbon dioxide on the upper part of the solution in the kettle was replaced with air, and measured according to the method in Example 12, and the carbon dioxide absorption amount was 1.5 mmol. The carbon dioxide absorption amounte by the above carboxylate solution at high partial pressure of carbon dioxide was compared with that of Example 12 of the present invention, indicating that a high carbon dioxide capture capacity can still be obtained at high partial pressure of carbon dioxide.

[0074] It can be seen from the above results that: [0075] 1) The halide salts of the organic cations in the present invention are bulk chemicals, and the price is several thousand yuan per ton; However, for the current market price of halides of tributylhexyl phosphine and tributyloctyl phosphine in the Comparative example (thousands of yuan per kilogram), it is obvious that the raw material price of the present invention is lower; [0076] 2) In Examples 1, 3 and 4 of the present invention, sodium 2-ethylhexanoate, potassium 2,2-dimethylhexanoate, lithium 2-ethylheptanoate, cesium 2-propylpentanoate, and sodium 2-hexyldecanoate are used for carbon dioxide absorption experiments. The inorganic salt metal ions such as lithium, sodium, potassium and cesium used have higher stability; [0077] 3) The present invention can obtain a higher carbon dioxide absorption amount (relative to the mass of the absorbent) under the appropriate water content, for example, the carbon dioxide absorption amount absorbed by per kilogram of absorbent is 2.12 and 1.11 moles per kilogram of carbon dioxide, respectively, per mole of tetramethylammonium 2-ethylhexanoate (molecular weight 217.3) and 2-ethylhexylphosphine (molecular weight 430.7) under the molar ratio of salt to water of 1: 1 and carbon dioxide of one atmosphere.

INDUSTRIAL APPLICATIONS

[0078] 1. The present invention is used to solve the problems of the existing system, such as corrosiveness, easy volatilization and high energy consumption. It can obtain higher carbon dioxide capture capacity under high temperature, low pressure and high pressure of carbon dioxide partial pressure.

[0079] 2. When the selected carboxylate aqueous solution absorbs carbon dioxide, its conjugate with carbon dioxide will be separated from water in a liquid or solid state, indicating that the conjugate of the selected carboxylate and carbon dioxide is stable in water,

[0080] 3. Carboxylates can be regenerated, which can be achieved by decompression at room temperature. Depending on different conditions, the absorption time can range from a few minutes to several hours. After the carbon dioxide is released, the carboxylates and water are miscible. Raising the temperature increases the regeneration rate.

[0081] 4. The cations in the carboxylate compounds used in the invention are substituted quaternary ammonium ion, substituted quaternary phosphorus ion, pyridinium ion, pyrrole ion, piperidinium ion, imidazolium ion and metal ion, which are inexpensive compared with the onium ions with higher price of tetraalkyl substituted phosphorus/ammonium, greatly reduces the cost of carbon dioxide capture.