Ultra cleaning of combustion gas including the removal of CO
View Patent ↗Ultra cleaning of combustion gas to near zero concentration of residual contaminants followed by the capture of CO 2 is provided. The high removal efficiency of residual contaminants is accomplished by direct contact cooling and scrubbing of the gas with cold water. The temperature of the combustion gas is reduced to 0-20 degrees Celsius to achieve maximum condensation and gas cleaning effect. The CO 2 is captured from the cooled and clean flue gas in a CO 2 absorber utilizing an ammoniated solution or slurry in the NH 3 —CO 2 —H 2 O system. The absorber operates at 0-20 degrees Celsius. Regeneration is accomplished by elevating the pressure and temperature of the CO 2 -rich solution from the absorber. The CO 2 vapor pressure is high and a pressurized CO 2 stream, with low concentration of NH 3 and water vapor is generated. The high pressure CO 2 stream is cooled and washed to recover the ammonia and moisture from the gas.
1. A method for removing CO 2 from a combustion gas stream, comprising:
cooling the gas stream to a first temperature in the range of 0-20 degrees Celsius;
cooling an ammoniated solution or slurry to a second temperature in the range of 0-20 degrees Celsius;
absorbing CO 2 from the cooled gas stream using the cooled ammoniated solution or slurry to provide a CO 2 rich ammoniated solution or slurry;
pressurizing the CO 2 rich ammoniated solution or slurry to a first pressure in the range of 30-2000 psi; and
heating the pressurized CO 2 rich ammoniated solution or slurry to a third temperature in the range of 50-200 degrees Celsius to separate CO 2 from the pressurized ammoniated solution or slurry, wherein the first pressure and third temperature are selected to prevent ammonia from escaping the liquid phase during the separation of CO 2 from the pressurized ammoniated solution or slurry and the separated CO 2 is in a form of a pressurized gas in the range of the first pressure.
2. The method of claim 1 , wherein the first temperature is in the range of 0-10 degrees Celsius.
3. The method of claim 1 , wherein the second temperature is in the range of 0-10 degrees Celsius.
4. The method of claim 1 , wherein the first and second temperatures are in the range of 0-10 degrees Celsius.
5. The method of claim 1 , wherein the ammoniated solution or slurry used to absorb the CO 2 is a CO 2 lean solution or slurry containing NH3, CO 2 and H2O or their aqueous species.
6. The method of claim 5 , wherein the CO 2 -lean solution or slurry has a NH 3 /CO 2 mole ratio in the range of 1.5-4.0.
7. The method of claim 5 , wherein the species in the NH 3 —CO 2 —H 2 O solution or slurry are concentrated such to contain dissolved species and suspended solids in the form of ammonium bicarbonate, NH 4 HCO 3 , crystals.
8. The method of claim 1 , wherein the ammoniated solution or slurry with the absorbed CO 2 is a CO 2 -rich solution having a NH 3 /CO 2 mole ratio in the range of 1.0-2.0.
9. The method as of claim 1 , wherein the first pressure is in the range of 150-400 psi.
10. The method of claim 1 , wherein the third temperature is in the range of 100 to 150 degrees Celsius.
11. The method of claim 1 , further comprising:
washing residual ammonia from the cooled gas stream using water after absorbing CO 2 from the cooled gas stream.
12. The method of claim 1 , further comprising:
washing residual ammonia from the cooled gas stream using an acidic solution after absorbing CO 2 from the cooled gas stream.
13. The method of claim 1 , wherein cooling the gas stream to the first temperature is performed by wet and direct cooling.
14. The method of claim 1 , wherein cooling the gas stream to the first temperature is performed in a series of cooling stages.
15. The method of claim 14 , wherein at least one cooling stage in the series of cooling stages includes a direct contact cooler.
16. The method of claim 1 , wherein absorbing CO 2 from the cooled gas stream using the cooled ammoniated solution or slurry is performed in a series of absorber stages.
17. A method for removing CO 2 from a combustion gas stream, comprising:
cooling the gas stream to a first temperature in the range of 0-20 degrees Celsius in a series of cooling stages;
cooling an ammoniated solution or slurry to a second temperature in the range of 0-20 degrees Celsius;
applying the cooled ammoniated solution or slurry to the gas stream in a series of absorbing stages to absorb CO 2 from the cooled gas stream and provide a CO 2 rich ammoniated solution or slurry;
pressurizing the CO 2 rich ammoniated solution or slurry to a first pressure in the range of 30-2000 psi; and
heating the pressurized CO 2 rich ammoniated solution or slurry to a third temperature in the range of 50-200 degrees Celsius to separate CO 2 from the pressurized ammoniated solution or slurry, wherein the first pressure and third temperature are selected to prevent ammonia from escaping the liquid phase during the separation of CO 2 from the pressurized ammoniated solution or slurry and the separated CO 2 is in a form of a pressurized gas.
18. The method of claim 17 , further comprising:
washing residual ammonia from the cooled gas stream using an acidic solution after absorbing CO 2 from the cooled gas stream.
19. A system for removing CO 2 from a combustion gas stream, comprising:
means for cooling the gas stream to a first temperature in the range of 0-20 degrees Celsius;
means for cooling an ammoniated solution or slurry to a second temperature in the range of 0-20 degrees Celsius;
means for absorbing CO 2 from the cooled gas stream using the cooled ammoniated solution or slurry to provide a CO 2 rich ammoniated solution or slurry;
means for pressurizing the CO 2 rich ammoniated solution or slurry to a first pressure in the range of 30-2000 psi; and
means for heating the pressurized CO 2 rich ammoniated solution or slurry to a third temperature in the range of 50-200 degrees Celsius to separate CO 2 from the pressurized ammoniated solution or slurry, wherein the first pressure and third temperature are selected to prevent ammonia from escaping the liquid phase during the separation of CO 2 from the pressurized ammoniated solution or slurry and the separated CO 2 is in a form of a pressurized gas.