Method for producing oxide layer material in landfill field for treating methane gas by using household refuse
US-2017266616-A1 · Sep 21, 2017 · US
US10926220B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10926220-B2 |
| Application number | US-201515506701-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 27, 2015 |
| Priority date | Aug 27, 2014 |
| Publication date | Feb 23, 2021 |
| Grant date | Feb 23, 2021 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Methods for enzyme-enhanced CO2 capture include contacting a CO2-containing gas with an aqueous absorption solution at process conditions—such as high temperature, high pH, and/or using carbonate-based solutions—in the presence of Thermovibrio ammonificans carbonic anhydrase (TACA) or functional derivative thereof for catalyzing the hydration reaction of CO2 into bicarbonate and hydrogen ions and/or catalyzing the desorption reaction to produce a CO2 gas. The TACA may be provided to flow with the solution to cycle through a CO2 capture system that includes an absorber and a stripper.
Opening claim text (preview).
The invention claimed is: 1. A method for absorbing CO 2 from a CO 2 -containing gas, the method comprising: (a) in an absorber, contacting the CO 2 -containing gas with an aqueous absorption solution to dissolve the CO 2 into the aqueous absorption solution; (b) providing a polypeptide having carbonic anhydrase activity that maintains at least 50% residual activity at 80° C. for 16 hours to catalyze the hydration reaction of the dissolved CO 2 into bicarbonate and hydrogen ions, wherein said polypeptide comprises an amino acid sequence having at least 70% sequence identity to SEQ ID NO: 6, wherein the SEQ ID NO: 6 is an amino acid sequence that lacks residues GGGAH (SEQ ID NO: 9) at a position corresponding to amino acid residues 2 to 6 of the wild-type Thermovibrio ammonificans carbonic anhydrase (TACA) sequence of SEQ ID NO: 4 resulting in an increased production level of said polypeptide as compared to the polypeptide of SEQ ID NO: 4, and (c) generating a bicarbonate ion-containing absorption solution. 2. The method of claim 1 , further comprising (d) treating the bicarbonate ion-containing absorption solution in a stripper to regenerate the absorption solution, wherein said treating comprises heating the absorption solution to provide conditions favorable to release CO 2 from the absorption solution, wherein the polypeptide of claim 1 catalyzes the dehydration reaction of bicarbonate ion into CO 2 ; and (e) generating a regenerated absorption solution and a CO 2 gas. 3. The method of claim 2 , further comprising cooling the regenerated absorption solution. 4. The method of claim 2 , wherein the polypeptide retains at least 80% residual activity for at least 20 days when subjected to continuous temperature cycling conditions comprising repeatedly exposing a solution of 0.2 g/L of the polypeptide in 1.45 M K 2 CO 3 pH 10 from a 40° C. water bath to a 77° C. water bath for 4 minutes. 5. The method of claim 2 , wherein the polypeptide is subject to thermal cycling comprising temperature swings ranging from 25° C. to 105° C., when cycling from absorption to stripping, wherein each thermal cycle comprises a temperature swing ranging from between 25° C. and 105° C., between 30° C. and 85° C., or between 40° C. and 60° C. 6. The method of claim 2 , wherein the temperature in the stripper is between 30 and 110° C. 7. The method of claim 1 , wherein the polypeptide is present in the absorption solution at a concentration ranges between 0.05 and 4 g/L. 8. The method of claim 1 , wherein the polypeptide is present in the absorption solution at a concentration ranges between 0.2 and 2 g/L. 9. The method of claim 1 , wherein the absorption solution comprises a monovalent metal carbonate. 10. The method of claim 9 , wherein the monovalent metal carbonate is sodium carbonate or potassium carbonate. 11. The method of claim 9 , wherein the monovalent metal carbonate is potassium carbonate present in the aqueous absorption solution at a concentration between about 1 M and about 2 M. 12. The method of claim 1 , wherein the pH of the aqueous absorption solution entering in the absorber is between about 8 and about 11. 13. The method of claim 1 , wherein the absorber is a packed column or a rotating packed bed (RPB). 14. The method of claim 1 , wherein the aqueous absorption solution comprises one or more absorption compounds selected from: a primary amine, a secondary amine, a tertiary amine, a primary alkanolamine, a secondary alkanolamine, a tertiary alkanolamine, a primary amino acid, a secondary amino acid, a tertiary amino acid, dialkylether of polyalkylene glycols, dialkylether or dimethylether of polyethylene glycol, an amino acid or a derivative thereof, monoethanolamine (MEA), 2-amino-2-methyl-1-propanol (AMP), 2-(2-aminoethylamino)ethanol (AEE), 2-amino-2-hydroxymethyl-1,3-propanediol (Tris or AHPD), N-methyldiethanolamine (MDEA), dimethylmonoethanolamine (DMMEA), diethylmonoethanolamine (DEMEA), triisopropanolamine (TIPA), triethanolamine (TEA), diethanolamine (DEA), diisopropylamine (DIPA), methylmonoethanolamine (MMEA), tertiarybutylaminoethoxy ethanol (TBEE), N-2-hydroxyethyl-piperzine (HEP), 2-amino-2-hydroxymethyl-1,3-propanediol (AHPD), hindered diamine (HDA), bis-(tertiarybutylaminoethoxy)-ethane (BTEE), ethoxyethoxyethanol-tertiarybutylamine (EEETB), bis-(tertiarybutylaminoethyl)ether, 1,2-bis-(tertiarybutylaminoethoxy)ethane and/or bis-(2-isopropylaminopropyl)ether, piperazine or a derivative thereof, piperazine or derivative thereof substituted by at least one alkanol group, or any combination thereof. 15. The method of claim 14 , wherein the concentration of the absorption compound is between 0.1 and 8 M. 16. The method of claim 1 , wherein the temperature in the absorber is between 10 and 98° C. 17. The method of claim 1 , wherein the polypeptide is immobilized on a support. 18. The method of claim 1 , wherein the polypeptide is non-immobilized or dissolved in the aqueous absorption solution. 19. The method of claim 1 , wherein the CO 2 -containing gas is combustion gas comprising CO, NOx, and/or SOx. 20. The method of claim 1 , wherein the CO 2 -containing gas is biogas and/or raw petroleum gas, or is derived from natural gas combustion or coal combustion.
Lyases (4.) · CPC title
Carbonate dehydratase (4.2.1.1), i.e. carbonic anhydrase · CPC title
Carbon oxides · CPC title
of CO2 · CPC title
Secondary amines · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.