Aminated magnesium oxide adsorbent and a method of capturing carbon dioxide
View Patent ↗An aminated magnesium oxide adsorbent, which is the reaction product of a magnesium oxide matrix having disordered mesopores and an amino silane, wherein amine functional groups are present on an external surface and within the disordered mesopores of the magnesium oxide matrix, and wherein the aminated magnesium oxide adsorbent has an average pore volume of 0.2 to 0.4 cm 3 /g. A method of making the aminated magnesium oxide adsorbent and a method of capturing CO 2 from a gas mixture with the aminated magnesium oxide adsorbent are also described.
1. An aminated magnesium oxide adsorbent, which is the reaction product of:
a magnesium oxide matrix having disordered mesopores; and
an amino silane;
wherein amine functional groups are present on an external surface and within the disordered mesopores of the magnesium oxide matrix; and
wherein the aminated magnesium oxide adsorbent has an average pore volume of 0.2 to 0.4 cm 3 /g.
2. The aminated magnesium oxide adsorbent of claim 1 , wherein the magnesium oxide matrix is prepared from precipitation of magnesium hydroxide from a solution of a magnesium salt and ammonium hydroxide, followed by calcination of the magnesium hydroxide at 350 to 450° C.
3. The aminated magnesium oxide adsorbent of claim 1 , wherein the magnesium oxide matrix has a BET surface area of 320 to 380 m 2 /g.
4. The aminated magnesium oxide adsorbent of claim 1 , wherein the magnesium oxide matrix has an average pore volume of 0.3 to 0.5 cm 3 /g and an average pore size of 3 to 6 nm.
5. The aminated magnesium oxide adsorbent of claim 1 , wherein the magnesium oxide matrix consists essentially of magnesium oxide.
6. The aminated magnesium oxide adsorbent of claim 1 , wherein the amino silane contains one amino group per molecule.
7. The aminated magnesium oxide adsorbent of claim 1 , wherein the amino silane is of formula (I)
wherein
R 1 is an optionally substituted alkoxy, an optionally substituted aryloxy, or a halo;
R 2 is an optionally substituted alkyl, an optionally substituted aryl, or an optionally substituted arylalkyl;
R 3 and R 4 are independently hydrogen, an optionally substituted alkyl, an optionally substituted aryl, or an optionally substituted arylalkyl;
n is an integer of 2 to 16; and
x is 0, 1, or 2.
8. The aminated magnesium oxide adsorbent of claim 7 , wherein R 1 is methoxy or ethoxy, R 2 is methyl, ethyl, phenyl, or benzyl, R 3 and R 4 are each hydrogen, n is 2 or 3, and x is 0 or 1.
9. The aminated magnesium oxide adsorbent of claim 1 , wherein the amino silane is 3-aminopropyl triethoxysilane.
10. The aminated magnesium oxide adsorbent of claim 1 , which has a magnesium content of 15 to 31 wt. %, an oxygen content of 40 to 50 wt. %, a carbon content of 17.5 to 30 wt. %, a nitrogen content of 1 to 6 wt. %, and a silicon content of 2 to 12 wt. %, each based on a total weight of the aminated magnesium oxide adsorbent.
11. The aminated magnesium oxide adsorbent of claim 1 , which has a BET surface area of 100 to 160 m 2 /g.
12. The aminated magnesium oxide adsorbent of claim 1 , which has an average pore size of 7 to 11 nm.
13. The aminated magnesium oxide adsorbent of claim 1 , which is crystalline by XRD.
14. The aminated magnesium oxide adsorbent of claim 1 , which has a CO 2 uptake capacity of 50 to 80 mg CO 2 per 1 g of the aminated magnesium oxide adsorbent at 30° C. and 1 atm.
15. A method of making the aminated magnesium oxide adsorbent of claim 1 , the method comprising:
precipitating magnesium hydroxide from a solution of a magnesium salt and ammonium hydroxide;
calcining the magnesium hydroxide at 350 to 450° C. for 6 to 24 hours to form the magnesium oxide matrix having disordered mesopores; and
aminating the magnesium oxide matrix with the amino silane at 60 to 100° C. for 12 to 48 hours.
16. The method of claim 15 , wherein a molar ratio of the ammonium hydroxide to the magnesium salt in the solution is 2:1 to 9:1, and wherein the precipitating is performed by heating the solution to 50 to 70° C. for 3 to 10 hours, followed by stirring the solution at 20 to 30° C. for 12 to 48 hours.
17. The method of claim 15 , wherein a weight ratio of the amino silane to the magnesium oxide matrix is 1.5:1 to 4:1.
18. A method of capturing CO 2 from a gas mixture comprising CO 2 and at least one other gas selected from the group consisting of hydrogen, oxygen, nitrogen, methane, and carbon monoxide, the method comprising:
contacting the gas mixture with the aminated magnesium oxide adsorbent of claim 1 to adsorb at least a portion of the CO 2 into the aminated magnesium oxide adsorbent, thereby forming a loaded aminated magnesium oxide adsorbent and a gas stream depleted in CO 2 compared to the gas mixture.
19. The method of claim 18 , wherein the gas mixture is a pre-combustion gas mixture comprising 15 to 50 vol. % of CO 2 , based on a total volume of the gas mixture.
20. The method of claim 18 , wherein the gas mixture is a post-combustion gas mixture comprising 5 to 15 vol. % of CO 2 , based on a total volume of the gas mixture.