Method for the separation of ammonia and carbon dioxide from aqueous solutions

Patent metadata

Field	Value
Publication number	US-9266745-B2
Application number	US-201013395262-A
Country	US
Kind code	B2
Filing date	Sep 1, 2010
Priority date	Sep 9, 2009
Publication date	Feb 23, 2016
Grant date	Feb 23, 2016

Abstract

The present invention relates to a method for contemporaneously recovering ammonia and carbon dioxide from an aqueous solution thereof, possibly comprising their condensates, in a synthesis process of urea, characterized in that it comprises a hydrophobic microporous membrane distillation phase of an aqueous solution comprising ammonia, carbon dioxide and their saline compounds or condensates, said distillation being carried out at a temperature ranging from 50 to 250° C. and a pressure ranging from 50 KPa to 20 MPa absolute, with the formation of a residual aqueous solution, possibly comprising urea, and a gaseous permeate stream, comprising ammonia, carbon dioxide and water. The present invention also relates to an apparatus for effecting the above method and a production process of urea which comprises the above method.

First claim

The invention claimed is:

1. A method for contemporaneously recovering ammonia and carbon dioxide from an aqueous solution in a urea synthesis process, the method comprising
distilling on a hydrophobic microporous membrane the aqueous solution comprising ammonia, carbon dioxide and, optionally, a saline compound or a condensate thereof, at a temperature of 50 to 250° C. and at a pressure of 50 KPa to 20 MPa absolute, to obtain a residual aqueous solution, optionally comprising urea, and a permeated gaseous stream comprising ammonia, carbon dioxide and water,
wherein
the aqueous solution is a recycled solution from a urea production process or an effluent coming from a urea synthesis reactor, and
the aqueous solution comprises 20 to 70% by weight of ammonia, 10 to 60% by weight of carbon dioxide and 10 to 70% by weight of water.

2. The method of claim 1 , wherein the aqueous solution further comprises 0 to 60% by weight of urea.

3. The method of claim 1 , wherein the distilling is performed at a temperature of 80 to 220° C.

4. The method of claim 1 , wherein
the aqueous solution comprises 5 to 40% by weight of ammonia, 2.5 to 20% by weight of carbon dioxide, and 10 to 60% by weight of urea, and
the distilling is performed at a temperature of 100 to 220° C. and a pressure of 10 to 18 MPa.

5. The method of claim 1 , wherein the aqueous solution comprises no urea and comprises 5 to 70% by weight of ammonia and 2.5 to 30% by weight of carbon dioxide, and
the distilling is performed at a temperature of 60 to 200° C. and a pressure of 1 to 10 MPa.

6. The method of claim 1 , wherein the aqueous solution is heated by irradiation with microwaves.

7. The method of claim 6 , wherein the irradiation of the aqueous solution is performed in such a way that a temperature of the aqueous solution increases along a direction of a stream of the aqueous solution.

8. The method of claim 1 , wherein the aqueous solution forms a contact angle with a material of the membrane equal to or greater than 90°.

9. The method of claim 1 , further comprising recycling the permeated gaseous stream within the urea synthesis process.

10. The method of claim 1 , wherein the distilling is performed in the presence of an additional carrier stream.

11. The method of claim 1 , wherein
the permeated gaseous stream is fed to a high-pressure condenser/separator for separating a non-condensed fraction which is fed to a decomposer,
the non-condensed fraction consists essentially of ammonia and carbon dioxide and is substantially free of water, and
the residual aqueous solution is fed to the decomposer for decomposing ammonium carbamate present in the residual aqueous solution and separating a second gaseous stream comprising ammonia, carbon dioxide and water vapour, which is fed to a medium pressure condenser/absorber.

12. The method of claim 1 , wherein
the permeated gaseous stream is fed to a high-pressure condenser/separator for separating a non-condensed fraction which is fed to a decomposer,
the non-condensed fraction consists of ammonia and carbon dioxide, and
the residual aqueous solution is fed to the decomposer for decomposing ammonium carbamate present in the residual aqueous solution and separating a second gaseous stream comprising ammonia, carbon dioxide and water vapour, which is fed to a medium pressure condenser/absorber.

Assignees

• Casara Paolo
• Gianazza Alessandro
• Saipem Spa

Inventors

• Casara Paolo
• Gianazza Alessandro

Classifications

• C02F2101/10

  Inorganic compounds · CPC title

• C02F2101/16

  Nitrogen compounds, e.g. ammonia · CPC title

• C02F1/44

  by dialysis, osmosis or reverse osmosis {(general membrane separation processes B01D61/00, membrane modules B01D63/00, electrodialysis C02F1/4693, combination of membrane modules and bioreactors C02F3/1268)} · CPC title

• C01C1/10 Primary

  Separation of ammonia from ammonia liquors, e.g. gas liquors {(as part of the ammonia synthesis process C01C1/04)} · CPC title

• C02F2103/36

  from the manufacture of organic compounds · CPC title