Aminated siliceous adsorbent from rice husk ash and a method of capturing carbon dioxide
US-11571681-B2 · Feb 7, 2023 · US
US11766658B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11766658-B2 |
| Application number | US-202218088509-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 23, 2022 |
| Priority date | Feb 5, 2020 |
| Publication date | Sep 26, 2023 |
| Grant date | Sep 26, 2023 |
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An aminated siliceous adsorbent, which is the reaction product of dried acidified rice husk ash having disordered mesopores and an amino silane, wherein amine functional groups are present on an external surface and within the mesopores of the dried acidified rice husk ash, and wherein the aminated siliceous adsorbent has a carbon content of 24 to 30 wt. %, based on a total weight of the aminated siliceous adsorbent. A method of making the aminated siliceous adsorbent and a method of capturing CO2 from a gas mixture with the aminated siliceous adsorbent.
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The invention claimed is: 1. A method of capturing CO 2 from a gas mixture, comprising: contacting the gas mixture with an aminated siliceous adsorbent to adsorb at least a portion of the CO 2 onto the aminated siliceous adsorbent, thereby forming a loaded aminated siliceous adsorbent and a gas stream depleted in CO 2 compared to the gas mixture, wherein the aminated siliceous adsorbent has disordered mesopores and a carbon content of 24 to 30 wt. %, based on a total weight of the aminated siliceous adsorbent, wherein the aminated siliceous adsorbent is a reaction product of: dried acidified rice husk ash having disordered mesopores, an oxygen content of 40 to 46 wt. % and a silicon content of 34 to 40 wt %, each based on a total weight of the dried acidified rice husk ash; and an amino silane; and wherein amine functional groups are present on an external surface and within the mesopores of the dried acidified rice husk ash. 2. The method of claim 1 , wherein the gas mixture further comprises at least one other gas selected from the group consisting of hydrogen, oxygen, nitrogen, methane, and carbon monoxide. 3. The method of claim 1 , 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. 4. The method of claim 1 , 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. 5. The method of claim 1 , wherein the gas stream depleted in CO 2 contains at least 25% less CO 2 by volume compared to a volume of CO 2 present in the gas mixture. 6. The method of claim 1 , wherein the amino silane contains one amino group per molecule. 7. The method 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 method 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 method of claim 1 , wherein the amino silane is 3-aminopropyl triethoxysilane. 10. The method of claim 1 , wherein the aminated siliceous adsorbent has an oxygen content of 35 to 41 wt. %, a silicon content of 28 to 34 wt. %, and a nitrogen content of 0.5 to 6 wt. %, each based on a total weight of the aminated siliceous adsorbent. 11. The method of claim 1 , wherein the aminated siliceous adsorbent has a surface area of 90 to 110 m 2 /g. 12. The method of claim 1 , wherein the aminated siliceous adsorbent has a pore volume of 0.14 to 0.22 cm 3 /g. 13. The method of claim 1 , wherein the aminated siliceous adsorbent has a mean pore diameter of 2.7 to 3.3 nm. 14. The method of claim 1 , wherein the aminated siliceous adsorbent has a CO 2 uptake capacity of 0.4 to 0.46 mmol/g at 298 K and 1 atm, a CO 2 uptake capacity of 0.5 to 0.6 mmol/g at 273 K and 1 atm, and a H 2 uptake capacity of 1 to 1.4 mmol/g at 77 K and 1 atm. 15. The method of claim 1 , wherein the aminated siliceous adsorbent has an ideal selectivity of CO 2 /N 2 of 20 to 24, CO 2 /H 2 of 10 to 14, and an ideal selectivity of CO 2 /CH 4 of 6 to 10.
Naturally occurring macromolecular compounds, e.g. humic acids or their derivatives · CPC title
by adsorption, e.g. preparative gas chromatography {(solid sorbent compositions B01J20/00, preparation of inorganic compounds or elements C01)} · CPC title
being less than 100 m2/g · CPC title
being in the range 100-500 m2/g · CPC title
being less than 0.5 ml/g · CPC title
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