COMBINED SYSTEM BASED ON MIXTURES OF IONIC LIQUIDS AND AMINO ACIDS TO ABSORB CARBON DIOXIDE

Abstract

The present invention describes a combined liquid absorbent system to capture gaseous CO.sub.2. The said combination is given by the mixture of an IL and an amino acid aqueous solution. This mixture has an improved CO.sub.2 absorption performance with respect to the separate components that are part of it. These components can be regenerated and reused in several absorption cycles without losing absorption capacity.

Claims

1. A liquid system, comprising: a mixture of ionized liquids, wherein an ionized liquid (IL) of the mixture of ionized liquids comprises a heterocyclic cation and an anion including a deprotonated amino acid, the heterocyclic cation being of a tetramethylammonium type and the deprotonated amino acid being of a lysinate type or a glycinate type; and amino acids to absorb carbon dioxide, the amino acids comprise an amino acid aqueous solution (AA) in a ratio IL:AA de 590%:905%. AA from about 5:90% to about 90:5%, the AA being of an alanine type, a lysine type or a glycine type.

2. The liquid system in accordance with claim 1, further comprising a solvent that comprises water.

3. The liquid system in accordance with claim 1, wherein the heterocyclic cation comprises one of imidazolium, pirazolio, piridinio o pirrolidinio. pyrazolium, pyridinium or pyrrolidinium.

4. The liquid system in accordance with claim 1, wherein the IL comprises an acyclic cation of the ammonium type, phosphonium type, or sulfonium type.

5. The liquid system in accordance with claim 1, wherein the IL absorbs carbon dioxide at a pressure between about 0.5 atmospheres and 20 atmospheres and a temperature between about 20 C. and 100 C.

6. The liquid system in accordance with claim 1, wherein a concentration of products in the solvent range from about 1% to 50%.

Description

BRIEF DETAILED DESCRIPTION OF THE INVENTION SCHEMES

[0014] In order to clearly understand the combined system of CO.sub.2 absorption using ILs and amino acids, which is the object of the present invention, the description of the figures featured in it is offered without limiting its scope:

[0015] FIG. 1 shows the diagram of the equipment used for the evaluation of CO.sub.2 absorbents consisting of a gas cell (A), a thermostat (B), a manometer (C), a stainless steel reactor with magnetic stirring (D), a vacuum pump (E) and a stirring plate (F). The temperature was measured with a thermocouple placed in the water bath (uncertainty below 0.1 K).

[0016] FIG. 2 presents the pressure behavior of CO.sub.2 versus time for the lysinate tetramethyl ammonium+3% aqueous alanine system. The evaluation conditions were 3 atmospheres of CO.sub.2 and 30 C. FIG. 2 describes the behavior of CO.sub.2 absorption for the mixture of compounds described in Example 1.

[0017] FIG. 3 exhibits the molar absorption capacity of CO.sub.2 in the IL systems. The evaluation conditions were 3 atmospheres of CO.sub.2 and 30 C.

DETAILED DESCRIPTION OF THE INVENTION

[0018] The present invention is a novel application for CO.sub.2 absorption from gaseous mixtures using a system of aqueous solutions of amino acids and ILs. In the best of our knowledge, these mixtures of components have not been reported for this application.

[0019] The preparation of the amino acid solutions using alanine, lysine and glycine is performed at 3 wt. % in distilled water meanwhile ILs based on tetramethylammonium are purified and until the time of use, they have no traces of residual solvents, which ensures that the CO.sub.2 absorption is due solely to the amino acid and the corresponding IL aqueous solution.

[0020] The composition of the liquid system consists of 5 grams of pure tetramethylammonium glycinate or tetramethylammonium lysinate and 5 grams of aqueous IL, 3 wt. % of the corresponding amino acid. The evaluation conditions are 30 C. and 3 atmospheres of CO.sub.2.

[0021] To measure the absorption capacity of a liquid system with respect to a gas (or gas mixture) under saturation conditions, a cell was designed and built to operate at constant volume and variable pressure, and to be immersed in a temperature-controlled bath. The cell is equipped with a magnetic stirrer. The previously described arrangement is called gas absorption system using liquid mixtures. Calculations are performed by using the ideal gas law.

[0022] Through the data collected from the pressure drop versus time experiment, keeping constant the temperature and amount of absorbent material, it is possible to know the amount of absorbed gas and thereby calculate the gas absorption capacity (CO.sub.2 in the case of this invention) of the system conformed by the aqueous solution of amino acid and the corresponding IL under saturation conditions.

[0023] FIG. 2 presents the typical performance for CO.sub.2 absorption using a liquid mixture of absorbent. The time in minutes is plotted on the horizontal axis and the pressure of the gas inside the cell is represented on the vertical axis. It is observed that as time passes by, the gas pressure tends to decrease to a constant value, which is the saturation pressure, and is the maximum level of absorbed CO.sub.2 under the employed conditions.

[0024] FIG. 3 shows a comparison of the absorption capacity of the pure ILs lysinate tetramethylammonium (LysTMA) and glycinate tetramethylammonium (GlyTMA), and mixtures thereof with the amino acids lysine (Lys), alanine (Ala) or glycine (Gly) in aqueous solution (3 wt. %). This absorption capacity is expressed in millimoles of CO.sub.2 per gram of absorbent. It is observed that the pure IL tetramethylammonium lysinate has a CO.sub.2 absorption capacity that is lower than those the mixtures thereof with aqueous amino acid; the behavior displayed by tetramethylammonium glycinate (GlyTMA) is similar. Furthermore, it should be noted that the capacity of tetramethylammonium lysinate and its mixtures is almost twice the capacity of the respective glycinate.

[0025] Table 1 shows a comparison between the results of the present invention and those reported in the literature. It is observed that monoethanolamine (MEA) has an intermediate absorption capacity evidenced by the results achieved with ILs and their mixtures. However, it is noteworthy to emphasize that the conditions are not the same, e.g., the concentration reported for MEA is 30 wt. %, and in the case of the present invention is 3 wt. %, which makes evident that the system proposed here employs a lower solute concentration.

EXAMPLES

[0026] Examples related to the combined liquid system for CO.sub.2 absorption based on ILs and amino acids, which is the object of the present invention and described above, are presented without limiting its technical scope.

[0027] Here, the general experimentation procedures to evaluate each combined system comprising a mixture of IL and aqueous amino acid are disclosed. The total amount of liquid in the present examples is fixed at 10 grams of sample when used as pure IL, namely tetramethylammonium lysinate (LysTMA) and glycinate tetramethylammonium (GlyTMA), and in the case of mixtures, the system was conformed with 5 grams of pure IL and 5 grams of aqueous amino acid solution (3 wt. %).

[0028] The isotherms for CO.sub.2 absorption were obtained at 303 K using an initial pressure of 3 atm FIG. 1 shows the diagram of the arrangement to carry out the experiments, which consists of a CO.sub.2 gas cylinder (A), a thermostat (B), a manometer (C), a stainless steel reactor with magnetic stirring (D), a vacuum pump (E) and a stirring plate (F). The temperature was recorded with a thermometer placed in the heating bath (uncertainty below 0.1 K).

Example 1

[0029] Following the general experimentation procedure, the absorption of a tetramethyl ammonium lysinate+3% aqueous alanine mixture was measured. The evaluation conditions were 3 atmospheres of CO.sub.2 and 30 C. In FIG. 1, the behavior of the pressure change versus time for this mixture is shown, where the CO.sub.2 absorption was 717.24 mmol of CO.sub.2/mol of absorbent.

Example 2

[0030] Following the general experimentation procedure, the absorption of a tetramethyl ammonium lysinate+3% aqueous lysine mixture was measured. The evaluation conditions were 3 atmospheres of CO.sub.2 and 30 C. The CO.sub.2 absorption was 704.7 mmol of CO.sub.2/mol of absorbent.

Example 3

[0031] Following the general experimentation procedure, the absorption of a tetramethyl ammonium lysinate+3% aqueous glycine mixture was measured. The evaluation conditions were 3 atmospheres of CO.sub.2 and 30 C. The CO.sub.2 absorption was 650.34 mmol of CO.sub.2/mol of absorbent.

Example 4

[0032] Following the general experimentation procedure, the absorption of a tetramethyl ammonium glycinate+3% aqueous lysine mixture was measured. The evaluation conditions were 3 atmospheres of CO.sub.2 and 30 C. The CO.sub.2 absorption was 350.36 mmol of CO.sub.2/mol of absorbent.

Example 5

[0033] Following the general experimentation procedure, the absorption of a tetramethyl ammonium glycinate+3% alanine aqueous mixture was measured. The evaluation conditions were 3 atmospheres of CO.sub.2 and 30 C. The CO.sub.2 absorption was 349.96 mmol of CO.sub.2/mol of absorbent.

Example 6

[0034] Following the general experimentation procedure, the absorption of a tetramethyl ammonium glycinate+3% aqueous lysine mixture was measured. The evaluation conditions were 3 atmospheres of CO.sub.2 and 30 C. The CO.sub.2 absorption was 365.83 mmol of CO.sub.2/mol of absorbent.

TABLE-US-00001 TABLE 1 Comparison of the CO.sub.2 absorption capacity Absorption capacity, Entry Absorbent mmol CO.sub.2/mol absorbent a Mono ethanol amine, 516 30 wt. % in aqueous solution * b LysTMA .sup. 612.67 c LysTMA + Ala 717.24 d LysTMA + Lys 704.70 e LysTMA + Gli 650.34 f GlyTMA .sup. 334.35 g GlyTMA + Ala 350.36 h GlyTMA + Lys 349.96 i GlyTMA + Gly 365.83 NOTES: 1. * Source: http://dx.doi.org/10.1155/2015/965015 2. .sup. TMA and TMA Gly were evaluated as pure compounds (without dilution). 3. The mixtures were evaluated with the amino acid at 3 wt. % in aqueous solution.