WO2013109895A1

WO2013109895A1 - Mixed salt co2 sorbent, processes for making and uses thereof

Info

Publication number: WO2013109895A1
Application number: PCT/US2013/022151
Authority: WO
Inventors: Esam Zaki Hamad; Wajdi Issam AL-SADAT; Luke Coleman; J.P. Shen; Raghubir Gupta
Original assignee: Saudi Arabian Oil Company; Research Triangle Institute
Priority date: 2012-01-20
Filing date: 2013-01-18
Publication date: 2013-07-25
Also published as: JP6121445B2; CA2861450C; JP2015510447A; EP2814592A1; US20130195742A1; KR20140127825A; US9539541B2; SG11201404191SA; CA2861450A1; CN104185498A; EP2814592B1

Abstract

A mixed salt composition which is useful as a CO₂ sorbent is described. The mixed salt composition comprises a Mg salt, and at least one Group IA element salt, where the Mg and Group IA element are present at a molar ratio of from 3:1 to 8:1. The resulting composition can adsorb about 20% or more of C0₂ in a gas. Via varying the molar ratios of the components, and the Group IA element, one can develop compositions which show optional functionality at different conditions. The composition is especially useful in the adsorptive capture of CO₂ on mobile sources, such as transportation vehicles, where it can be recovered during regeneration of the adsorbent composition and the CO₂ used as a coolant gas, as a reactant in manufacture of fuel, and so forth.

Description

MIXED SALT CO₂ SORBENT, PROCESSES FOR

MAKING AND USES THEREOF

RELATED APPLICATIONS

[01] This application claims priority from U.S. Provisional Application Nos. 61/588,927 filed January 20, 2012 and 61/673,395 filed July 19, 2012, both incorporated by reference in their entireties.

FIELD OF THE INVENTION

[02] This invention relates to materials which are useful in removing CO₂ from gas. More particularly, it relates to mixed salt compositions which act as sorbents for the CO₂, methods for making these materials and their uses. These adsorbents are useful for removing CO₂ from exhaust gas stream in both stationary and mobile applications, such as transportation vehicles, and so forth.

BACKGROUND AND PRIOR ART

[03] Reduction of CO₂ emissions is a key goal for all scientific disciplines, acerbated by the growing evidence of, and concern over, climate change induced by CO₂. It is estimated that, in the United States, about 1/3 of CO₂ emissions are generated by the transportation sector through combustion of fuels.

[04] One approach to mitigating these emissions is to capture as much CO₂ as possible from exhaust gases, prior to their release to the atmosphere. Post-combustion, CO₂ capture technologies are being developed for application to stationary sources of CO₂. These sources include coal, and natural gas fired power plants, as well as processes for production of materials as diverse as cement and steel. This invention as described herein is useful in such applications, but also in mobile source applications.

[05] Primary challenges for developing useful processes for capture of CO₂ from stationary sources, include energy demand, and capital expenditures. Developing technologies which address CO₂ capture from mobile sources involves these factors, as well as space limitation, the dynamics of operating conditions, parameters such as high temperature and low pressures, and so forth. High temperatures and low pressures are especially important considerations, because these are outside of the operating and optimum ranges of most CO₂ capture technologies.

[06] It is a purpose of the invention described herein to provide an effective, low cost CO₂ "scrubbing" technology which addresses these issues. How the invention achieves this will be seen in the disclosure which follows.

SUMMARY OF THE INVENTION

[07] The invention relates to a mixed salt, solid sorbent composition which is useful in removing CO₂ from gases. The composition may be regenerated easily, and thus is useful in continuous scrubbing processes. Further, it is useful in removal of CO₂ from both mobile and stationary applications. An important feature of the invention is that it is useful in the removal of CO₂ from gas mixtures at ambient or near ambient pressures, and at temperatures ranging from about 50°C to about 400°C, with release of the CO₂ at temperatures of from about 150°C to about 500°C.

[08] The mixed salt sorbent compositions of the invention contain alkaline earth and alkali metals, in salt form and at a range of ratios relative to each other. Preferably, the alkaline earth metal is represented by magnesium (Mg), while the alkali metal is one of the "group IA" elements, i.e., Li, Na, K, or Rb.

[09] As used herein, the term "stationary applications" includes coal, oil, and gas-fired power generating plants, steam boilers for commercial and industrial use, heat plants and other such installations that produce CO₂ from the combustion of hydrocarbon fuels.

[10] The term "mobile sources" includes internal combustion engines used to power all types of vehicles such as automobiles, trucks, buses, trains, boats, and airplanes that produce an exhaust gas stream containing CO₂ from the combustion of hydrocarbon fuels. DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

EXAMPLE 1

[11] This example details the preparation and use of a CO₂ sorbent according to the invention.

[12] An amount (395g) of magnesium carbonate hydroxide (MgC0₃ · Mg(OH>2 x H2O) was added to 800 ml of a solution of sodium carbonate (42.18 g) and sodium nitrate (21.63 g) dissolved in deionized water. This produced a mixed salt slurry which was stirred for 30 minutes. The slurry was then covered and allowed to sit for 16 hours at ambient temperature, after which it was dried, at 120°C, for 16 hours, to form a dry cake of MgO:Na2C03:NaN03. Analysis showed a mass ratio of 75.8:16:8.2 and a molar ratio of Mg:Na of about 4.8. This dry cake was then calcined by heating from 120°C to 450°C, at a ramp rate of 3°C/minute, followed by 450°C for 4 hours. The calcined cake was crushed and sieved to collect a 150-425 mesh fraction, which was then tested.

[13] The testing involved loading a packed bed reactor with 6g of the sorbent described supra, with inert SiC added to occupy any remaining volume. A conventional gas analyzer was used to measure the concentration of CO₂ leaving the reactor. The reactor was then activated by heating it to 450°C, at a rate of 10°C/minute, using a flow of N₂ and was held at this temperature until the concentration of CO₂ in the effluent dropped below 0.1 %. When the CO₂ concentration dropped below 0.1 %, the reactor was cooled to the lowest adsorption temperature tested and then a simulated exhaust gas (13% CO₂, 13% H₂O, remainder N₂), was added to the reactor as a feedstream. The concentration of CO₂ in the gas effluent was measured continuously and the adsorption phase was continued, until the concentration of CO₂ in the effluent was 90% of the concentration in the feed gas, i.e., the "90% break through." When this point was reached, the feed gas was changed to pure N₂, and its temperature was ramped at 5°C/minute to 450°C. The reactor itself was maintained at 500°C and until the effluent gas had a CO₂ concentration below 0.1% vol., or for 2 hours, so as to regenerate the sorbent. The reactor temperature was then decreased to the desired adsorption temperature, and the process was repeated.

[14] Figure 1 shows the amount of CO₂ loaded on the sorbent, over a temperature range of 200-425 °C, at 25°C increments.

EXAMPLE 2

[15] The prior example described the preparation of the CO₂ sorbent via gelation. This example describes a preparation method using precipitation, to form the same mixed salt composition.

[16] A solution of 233.4 g of Na₂CO₃ in 3000 ml deionized water was placed in a 5.0 liter plastic beaker, and stirred vigorously with a mechanical agitator. A second solution, of 188.4 g Mg(N0₃)₂ : 6 H₂O in 500 ml of deionized water, was pumped into the first solution, at a rate of approximately 30 ml/minute. A slurry resulted which was stirred for an hour. The slurry was stored, overnight, as described supra, and then filtered to yield a wet precipitate cake. About 3200 mls of filtrate were collected. This was dried, at 120°C for 24 hours to form a dry cake, which was treated a described in the first example, supra. The sorbent was then tested, as in Example 1. Figure 2 shows these results.

[17] In additional tests, the effect of the alkali element in the mixed salt sorbent composition was evaluated by using Li, Na, or K salts to prepare the final products. Salts were prepared in the manner set forth, supra, using a molar ratio of Mg : alkali metal of 6:1. The resulting products were tested for their ability to remove CO₂ from the simulated exhaust gas described supra. Adsorption was carried out at temperatures ranging from 100 - 450°C, at GHSV of 3,125/hour. The sorbents were regenerated by ramping temperatures to 450°C, at a rate of 10°C/minute, at a GHSV of 2500/hour.

[18] Figure 3 presents these results. While Na presents the best range of operation, the other alkali metals tested function well at different temperatures. [19] In yet further experiments, the effect of the source of magnesium on the resulting sorbent was tested. The mixed salt compositions of the invention should have either Mg₂CO₃ or MgO as a component thereof. Hence, in the reaction producing these sorbents, one selects a Mg compound is selected which will, preferentially, lead to one of these.

[20] Mg(NO₃)₂, MgO, and Mg(OH)2 were all tested, using the same parameters of Examples 1 and 2.

[21] Figure 4, which presents these results, shows that the nitrate salt produced a sorbent with a significantly greater ability to adsorb CO₂.

[22] It is noteworthy that Mg(NO₃)₂ has significantly greater solubility in water than the other compounds. The differences in solubility also indicate that the final products result from different reactive mechanisms. The nitrate salt, for example, participates in anion exchange with the sodium salts, whereas the oxide and hydroxide do not Hence, the more soluble the magnesium salt, the greater the adsorption ability of the final product. Mg(NO₃)₂, MgCl₂, Mg(CH₃COO)₂, and other highly soluble magnesium salts are thus preferred in making the sorbents of the invention.

[23] Further experiments were carried out to understand the role of Na in the adsorbence process. These studies were motivated by the recognition that, when CO₂ is adsorbed onto the compositions, it is loaded in the form of MgCO₃, while the sodium species do not store the CO₂.

[24] Sorbents were prepared, as described, supra, using Mg:Na molar ratios of 3:1 to 8:1, and were tested as described in these examples.

[25] It was found that when the Mg:Na ratio was from 8:1 - 6:1, the performance followed that of the examples, i.e., CO₂ loading capacity increased with adsorption temperature, reaching a maximum of about 13 wt%, at 350°C, followed by a rapid decrease in capacity as temperatures increased. [26] Decreasing the Mg:Na ratio to 4:1 - 3:1 impacted loading capacity significantly; however, a decrease in Na content also resulted in a shift to maximum adsorbency at 250°C, as shown in Figure 5. These findings suggest that different mechanisms are involved.

[27] An additional process parameter which was investigated in the study of the invention was the concentration of the reactants in the precipitating solution.

[28] Comparative tests were undertaken where, as above, the molar ratio of Mg:Na remained 6:1, but where the concentration of the reactants in the solution was 0.05, 0.1, 0.2, and 0.3M. Reactions proceeded as per Example 2, supra, to precipitate mixed salt sorbent materials. The resulting materials were then tested as in Examples 1 and 2.

[29] The results, set forth in Figure 6, shows that concentration had a profound impact on the performance of the sorbents. All functioned, but had optional activity at different temperatures, with a decrease in concentration reducing peak CO₂ loading temperature to from 250°C to 275°C, as well as an increase in CO₂ loaded on the sorbent, from about 12-13 wt% to about 20 wt%.

[30] While the experiments, supra, used Na₂CO₃ as a precipitating agent, others can be used, as was exemplified with (NH₄)₂CO₃.

[31] To prepare the sorbents with Na₂CO₂, the precipitating agent was added slowly in the form of a solution, to a solution of MgNO₃. For (NH₄)₂CO₃, this was added to a solution of MgNO₃ and Na₂CO₃. The Mg:Na molar ratio of 6: 1 was maintained.

[32] The results, depicted in Figure 7 showed that the product obtained with Na₂CO₃ exhibited a broad range of activity, whereas that prepared with (NH₄)₂CO₃ showed a very sharp spike in activity at 300°C, and very little activity at other temperatures. These results suggest that changes in the precipitating agent can be used to prepare sorbents for different applications. [33] The foregoing disclosure sets forth various features and embodiments of the invention, including a mixed salt composition useful as a sorbent for gaseous CO₂. The composition of the invention comprises a mixed salt of a magnesium compound, such as MgCC>3 or MgO, and at least one salt of a Group IA metal, wherein the molar ratio of Mg to the Group IA metal may range from 8:1 to 3:1, and is preferably from 6:1 to 4:1. The adsorbents are useful both in stationary and mobile applications for the removal of CO₂ from the exhaust gas stream and the recovery of substantially pure CO₂ that can be compressed for temporary storage pending its ultimate disposition. Following desorption of the CO₂, the regenerated adsorbent can then be revised, without substantial loss in adsorbent capacity during a significant number of cycles.

[34] As noted, the magnesium compound is preferably MgO, and the at least one salt of a Group IA metal is preferably a carbonate, and/or a nitrate salt. An especially preferred composition of the invention is MgO:Na₂CO₃:NaNO₃, where the molar ratio of Mg:Na is about 4.8. Salts of Li, , or Rb may replace the sodium salts in the preferred composition.

[35] The mixed salt sorbents of the invention can be made via, e.g., a gelation reaction, as in Example 1, or preferably a precipitation reaction. To elaborate, a magnesium salt and a Group IA metal salt are prepared in solution form, and combined to form a reactive mixture. This reaction may optionally be carried out with a precipitating agent. The salts are chosen such that, upon reacting with each other, MgO or MgCO₃ is formed in the precipitate. Preferably, a highly soluble Mg compound is used, such as MgO itself, Mg(OH)2, or most preferably, Mg(NO₃)₂. As noted supra, MgCl₂ or Mg(CH₃COO)₂ may also be used. Once the Mg salt is chosen, the skilled artisan may determine what Na salt or salts will react therewith to produce the desired MgO / MgCO₃.

[36] The examples, supra, describe two methods for making the sorbent, i.e., gelation and co-precipitation, or "precipitation." In the latter method, an Mg salt, and a Group IA metal salt, are dissolved in water, and then a precipitant is added, resulting in precipitation of the sorbent powder. This is the easier method to use in the lab, but it requires large quantities of water, batch yields are low, and material preparation is expensive. The gelation methodology requires greater care, with the 'trade off" of less water usage, higher yields, and reduced preparation costs.

[37] Following preparation of the sorbent powder, it can be made into an extrudate, either via adding a binder, such as boehmite, or via special preparative techniques known in the art, which result in a loss in sorbency; however, the technique is useful for keeping pressure drops low, in packed beds, and for rendering handling of the material easier.

[38] In tests summarized here, higher capacity was found in extrudates without binder, and these achieved high CO₂ loads (about 20 wt% at 300°C). The crush strength of such binder-free extrudates without binder was found to be 0.51 MPa, equivalent to those extrudates prepared with boehmite (0.55 MPa).

[39] On an industrial level, extrusion runs are nearly continuous, with continuous extraction and conveyance on, e.g., a belt convection dryer. Again, in experiments only summarized here, different drying rates were tested, and it was found that a rate of about 0.3°C/minute results in an extrudate with reasonable crunch strength. Increasing the drying rates did in fact decrease the strength of the resulting product.

[40] The reaction is carried out with concentrations of the reactive salts which provide for a ratio of Mg:Group IA metal of from 3:1 to 8:1, most preferably from 4:1 to 6:1. The choice of ratios is one left to the artisan because, as noted supra, by varying the ratio one produces sorbents with different properties. Knowing the conditions under which the sorbent will operate will determine the ratios employed. Optionally, a precipitating agent may be added to facilitate the reaction, such as NaNO₃. The precipitating agent is preferably a salt of a Group IA metal.

[41] The invention also comprehends methods for removing CO₂ from a gas or gas mixture, such as an exhaust gas stream produced by the combustion of a hydrocarbon fuel, by contacting the gas or gas mixture with the mixed salt sorbent described supra, at a temperature which ranges from about 100°C to about 450°C, preferably from about 250°C to about 350°C, for a time sufficient for the sorbent to remove a portion of the CO₂ therefrom. In practice, the sorbent will become "saturated" by the CO₂, and this can be detennined by measuring the content of CO₂ in gas after it has contacted the sorbent and comparing this value to the amount of CO₂ in the gas prior to the contact. When it is evident that CO₂ is not being removed to the extent desired, the sorbent can be regenerated by indirect heat exchange, e.g., with the hot exhaust gas stream which is at an elevated temperature, e.g., about 500°C. Again, by measuring the amount of CO₂ which is contained in the exiting gas, the ordinary skilled artisan can determine when the sorbent has been regenerated and can be reused.

[42] In practice, the removed CO₂ can be compressed and temporarily stored on board the mobile source until it is removed for permanent disposition, such as underground storage. Alternatively, the CO₂ can be put to use in various ways. For example, the process described herein, in addition to removing CO₂, results in the accumulation of condensed H₂O. These two species can be fed into a reactor or other means for generating fuel which, in turn, can be used, e.g., to power the CO₂ producing system described herein. Of course, if the fuel is not used as it is produced, it, also can be accumulated and stored for later use.

[43] The stored CO₂ can be used, e.g., as a refrigerant gas, and then channeled for cooling and/or air conditioning. The captured CO₂ gas released from the adsorbent can be reacted with the condensed water recovered from the exhaust gas stream to form a hydrogen-based fuel which can in turn be used, e.g., to power the ICE of the vehicle in which the CO₂ and H₂O were produced. Any solar energy to which the vehicle or other mobile source was exposed can also be stored and used to facilitate this reaction.

[44] In addition, means can be provided in the system for cooling the CO₂, thereby permitting its use as a coolant or refrigerant for use in the system.

[45] Other facets of the invention will be clear to the skilled artisan and need not be reiterated here.

[46] The terms and expression which have been employed are used as terms of description and not of limitation, and there is no intention in the use of such terms and expression of excluding any equivalents of the features shown and described or portions thereof, it being recognized that various modifications are possible within the scope of the invention.

Claims

1. A mixed salt composition useful as a sorbent for CO₂. comprising:

(i) a magnesium salt, and

(ii) at least one salt of a Group IA element wherein (i) said magnesium salt and (ii) said Group IA element salt are present in a molar ratio of from about 8:1 - 3:1.

2. The mixed salt composition of claim 1, wherein (i) and (ii) are present in a ratio of from 6:1 - 4:1.

3. The mixed salt composition of claim 1 , wherein (i) is MgCO₂ or MgO.

4. The mixed salt composition of claim 3, wherein (i) is MgO.

5. The mixed salt composition of claim 1 , wherein (ii) is a carbonate or a nitrate.

6. The mixed salt composition of claim 1 , wherein (ii) is a Na, Li, K, or Rb salt

7. The mixed salt composition of claim 1, wherein salt composition further comprises a sodium salt.

8. The mixed salt composition of claim 1, wherein (i) is Na₂CO₃ or NaNO₃.

9. The mixed salt composition of claim 1, of formula MgO:Na₂CO₃:NaNO₃.

10. A process for making the mixed salt composition of claim 1, comprising combining solutions of (i) a magnesium salt and (ii) a Group IA element salt to form a reaction mixture, under conditions favoring fonriing a precipitation product therefrom.

11. The process of claim 10, further comprising adding a precipitating agent

12. The process of claim 10, wherein (i) is a solution of MgO, Mg(OH)₂, Mg(NO₃)₂, MgCl₂, or Mg(CH₃COO)₂.

13. The process of claim 10, wherein (i) is a solution of Mg(NO₃)₂.

14. The process of claim 10, wherein (i) and (ii) are selected so as to form MgO or MgCO₂ therefrom.

15. A method for removing CO₂ from a gas or gas mixture, comprising contacting the mixed salt composition of claim 1 with said gas or gas mixture at a temperature of from about 100°C to about 450°C, for a time sufficient for said mixed salt composition to remove a portion of CO₂ therefrom.

16. The method of claim IS, wherein said temperature is from about 250°C to about 350°C.

17. The method of claim IS, further comprising contacting said mixed salt composition with an inert gas to removed any CO₂ adsorbed therein.

18. The method of claim 17, wherein said inert gas is N₂.

19. The method of claim 17, comprising contacting said inert gas to said mixed salt composition at a temperature of about 500°C.

20. The method of claim IS, further comprising placing said mixed salt composition on a mobile source and effecting adsorption of CO₂ from an internal combustion engine's exhaust gas stream produced via combustion of hydrocarbon fuel on said mobile source.

21. The method of claim 20, comprising releasing the adsorbed CO₃ to regenerate the composition by heat exchange with the hot exhaust gas stream discharged from the engine.

22. The method of claim 20, wherein said mobile source is a transportation vehicle.

23. The method of claim 21, wherein said transportation vehicle is an automobile, truck, bus, train, or boat, and the fuel is gasoline or diesel fuel.