METHOD FOR THE MANUFACTURE OF UREA

Abstract

A method for producing urea. A methane-containing feed gas stream is reacted with oxygen by partial oxidation to form a synthesis gas stream containing hydrogen and carbon monoxide. The carbon monoxide is reacted with water in a water gas-shift reaction to form carbon dioxide and hydrogen. The synthesis gas stream is separated into a first synthesis gas substream a second synthesis gas substream. The first synthesis gas substream is subjected to pressure-swing adsorption to separate hydrogen and the second synthesis gas substream is subjected to temperature-swing adsorption to separate carbon dioxide. The separated is reacted with nitrogen to form ammonia and the ammonia is reacted with the carbon dioxide to form urea.

Claims

1. A method for producing urea, comprising the steps: reacting a methane-containing feed gas stream with oxygen by partial oxidation to form a synthesis gas stream comprising hydrogen and carbon monoxide, reacting the carbon monoxide of the synthesis gas stream in a water gas-shift reaction with water to form carbon dioxide and hydrogen, dividing the synthesis gas stream into a first synthesis gas substream and a second synthesis gas substream, subjecting the first synthesis gas substream to a pressure-swing adsorption to separate hydrogen from the first synthesis gas substream, subjecting the second synthesis gas substream to a temperature-swing adsorption to separate carbon dioxide from the second synthesis gas substream, reacting the hydrogen separated from the first synthesis gas substream with nitrogen to form ammonia, and reacting the ammonia with the carbon dioxide separated from the second synthesis gas substream to form urea.

2. The method according to claim 1, wherein the carbon dioxide separated from the second synthesis gas substream is provided at a pressure of at least 10 bar.

3. The method according to claim 2, wherein the carbon dioxide is provided at a pressure of at least 20 bar.

4. The method according to claim 3, wherein the carbon dioxide is provided at a pressure of at least 50 bar.

5. The method according to claim 1, wherein the carbon dioxide separated from the second synthesis gas substream is provided stoichiometrically to the step of reaching the ammonia with the carbon dioxide to form urea, and wherein the ammonia is completely reacted to form urea.

6. The method according to claim 1, wherein, the step of subjecting the second synthesis gas substream to a temperature-swing adsorption comprises adsorbing then desorbing the carbon dioxide from the second synthesis gas substream using an adsorbent that is heated and cooled indirectly.

7. The method according to claim 6, wherein the adsorbing and desorbing of the carbon dioxide during temperature-swing adsorption comprises one cycle and wherein the time for one cycle is less than 360 minutes.

8. The method according to claim 7, wherein the time for one cycle is less than 240 minutes.

9. The method according to claim 8, wherein the time for one cycle is less than 180 minutes.

10. The method according to claim 1, wherein the step of subjecting the first synthesis gas substream to a pressure-swing adsorption comprises adsorbing CO.sub.2 and CO present in the first synthesis gas substream onto an adsorber at a first pressure, regenerating the adsorber at a second pressure that is lower than the first pressure to desorb the CO.sub.2 and CO, and removing the desorbed CO.sub.2 and CO by purging with production of an off-gas.

11. The method according to claim 10, wherein the off-gas is used as fuel for heating the feed gas stream or to produce or superheat steam.

12. The method according to claim 10, wherein the a temperature-swing adsorption produces an off-gas comprising H.sub.2 and CO, wherein the off-gas is subjected to a pressure-swing adsorption to produce additional hydrogen for use in the formation of the ammonia.

13. The method according to claim 12 wherein the off-gas from the temperature-swing adsorption is subjected to the pressure-swing adsorption together with the first synthesis gas substream.

14. The method according to claim 12 wherein the off-gas from the temperature-swing adsorption is mixed with the off-gas from the pressure-swing adsorption and used as fuel.

15. The method according to claim 1, wherein the carbon dioxide separated in the temperature-swing adsorption includes impurities and wherein the impurities are removed in a purification step, upstream of the reaction to form urea.

16. The method according to claim 15, wherein the impurities are H.sub.2, CH.sub.4, or CO.

17. The method according to claim 15, wherein the purification step is a catalytic oxidation.

18. The method according to claim 1, wherein the synthesis gas stream is cooled upstream or downstream of the water gas-shift reaction.

19. The method according to claim 18, wherein the synthesis gas stream is cooled with water, from a manufacture of process steam.

20. The method according to claim 18, wherein heat created during the cooling of the synthesis gas stream is used to regenerate an adsorber in the temperature-swing adsorption.

21. The method according to claim 1, wherein the oxygen is manufactured by cryogenic separation of air, wherein the cryogenic separation of air also produces nitrogen, and wherein the nitrogen produced is reacted with the hydrogen to form ammonia.

22. The method according to claim 1, further comprising passing the feed gas stream through an adsorber unit upstream of the partial oxidation to adsorb sulphur compounds.

23. The method according to claim 1, wherein the synthesis gas stream is dried downstream of the water gas-shift reaction and upstream of the pressure-swing adsorption and the temperature-swing adsorption.

24. The method according to claim 22, wherein the first synthesis gas substream is dried downstream of the water gas-shift reaction and upstream of the pressure-swing adsorption and wherein the second synthesis gas substream is dried downstream of the water gas-shift reaction and upstream of the temperature-swing adsorption.

25. A plant for producing urea, comprising a POX reactor for reacting a methane-containing feed gas stream with oxygen by partial oxidation to form a synthesis gas stream comprising hydrogen and carbon monoxide, a water gas-shift reactor downstream of the POX reactor for reacting the carbon monoxide in a water gas-shift reaction with water to form carbon dioxide and hydrogen, means to divide the synthesis gas stream from the water gas-shift reactor into a first synthesis gas substream and a second synthesis gas substream, a pressure-swing adsorption unit for subjecting the first synthesis gas substream to pressure-swing adsorption, wherein hydrogen is separated from the first synthesis gas substream, a temperature-swing adsorption unit for subjecting the second synthesis gas substream to temperature-swing adsorption, wherein carbon dioxide is separated from the second synthesis gas substream, an ammonia reactor for reacting hydrogen from the first synthesis gas substream with nitrogen to form ammonia, and a urea reactor for reacting ammonia with carbon dioxide from the second synthesis gas substream to form urea.

Description

[0041] Further features and advantages of the invention will be explained hereinafter in the description of the figures of exemplary embodiments of the invention with reference to the figures.

[0042] FIG. 1 shows a schematic depiction of a method according to the invention for producing urea.

[0043] FIG. 2 shows a schematic depiction of separating off CO.sub.2 and H.sub.2 from a synthesis gas manufactured in the method according to the invention.

[0044] FIG. 1 shows a schematic depiction of a plant and/or of a method for producing urea.

[0045] In this case, a feed gas stream NG comprising, e.g., CH.sub.4 (e.g. in the form of natural gas), before a reaction to form synthesis gas (comprising H.sub.2 and CO) S by partial oxidation 20 is subjected to a desulphurization 30 and then, by means of partial oxidation 20, in the presence of oxygen, and also, in particular steam W, is reacted to form a synthesis gas stream S that comprises H.sub.2 and CO, and also further, in particular CH.sub.4, H.sub.2O and CO.sub.2.

[0046] The synthesis gas stream S is hereafter subjected to a water gas-shift reaction 40 (see above) and cooled with water, wherein said steam W can be manufactured. In principle, heat arising during the cooling of the synthesis gas S can also be used for regenerating the adsorbers in the temperature-swing adsorption 51 described further below (cf. FIG. 2).

[0047] The synthesis gas stream S is in addition dried, wherein, hydrogen and carbon dioxide of the synthesis gas stream S are separated. (50), wherein the hydrogen is reacted (60) with nitrogen to form ammonia, and wherein the carbon dioxide is finally reacted with the ammonia that is manufactured to form urea.

[0048] The oxygen for the POX 20 is manufactured by cryogenic separation 10 of air L, wherein, also the nitrogen is obtained that is required for the ammonia synthesis 60.

[0049] According to FIG. 2, the hydrogen and carbon dioxide are separated off 50, preferably in such a manner that the shifted synthesis gas stream S is subdivided into a first and second synthesis gas substream S, S, wherein the first synthesis gas substream S is subjected to a pressure-swing adsorption 51, wherein hydrogen is separated off from the first synthesis gas substream S, and wherein the second synthesis gas substream S is subjected to a temperature-swing adsorption 52 (see above) that is heated and/or cooled, preferably at least in part indirectly, e.g. via a heat-carrier medium that is not in direct contact with the adsorbent, wherein carbon dioxide is separated off from the second synthesis gas substream S. The cycle times of such a temperature-swing adsorption are usually short and are in the range from 2 to 6 hours. The hydrogen that is separated off is then reacted together with the nitrogen to form ammonia 60 that in turn is reacted with the CO.sub.2 that is separated off to form urea 70. Preferably, the CO.sub.2 V arriving from the temperature-swing adsorption 52 is still further purified 53 upstream of the urea synthesis 70, in particular in order to remove impurities present therein such as, e.g., H.sub.2, CH.sub.4 and CO, methanol.

[0050] In the pressure-swing adsorption 51 for separating off the hydrogen from the first synthesis gas substream S, CO.sub.2 and CO and also possibly further components (such as, e.g. CH.sub.4) that are present in the first synthesis gas substream are adsorbed on an adsorber at a first pressure, wherein, preferably the adsorber is regenerated at a second pressure which is lower than the first pressure, wherein the adsorber components are desorbed, and wherein the adsorber, for removing the desorbed components, is purged, with manufacture of an off-gas A. Preferably, a plurality, in particular two or four, adsorbers are used in the pressure-swing adsorption 51, in order that as far as possible one adsorber can always be operated in the adsorption mode in such a manner that hydrogen can be released semi-continuously.

[0051] The off-gas A from the pressure-swing adsorption 51 can be used, e.g. as fuel, wherein, e.g. the off-gas A can be burnt for heating the feed gas stream NG and/or for producing and/or superheating steam.

[0052] In the temperature-swing adsorption 52, CO.sub.2 is adsorbed at a low first temperature on an adsorber and desorbed at a higher second temperature, for which the necessary energy E is provided. The residual gas arising in the adsorption of CO.sub.2 and/or off-gas A that comprises H.sub.2 and CO, can, together with the first synthesis gas substream S, be run into the pressure-swing adsorption 51 or can be mixed with the off-gas A from the pressure-swing adsorption 51 and, therewith, be used together as fuel.

[0053] On account of the separation according to the invention of CO.sub.2, said CO.sub.2, after the separation, is advantageously present at a high pressure of preferably at least 20 bar, and so correspondingly energy can be saved for the otherwise necessary compression of the CO.sub.2 for the purpose of urea synthesis. This is principally due to the fact that regeneration is performed during the temperature-swing adsorption by means of heating the adsorbent, and so in comparison the pressure drop occurring during regeneration in the pressure-swing adsorption is avoidable.

[0054] In addition, in the presence of the CO.sub.2 purification 53 by catalytic oxidation, CO.sub.2 arriving from the temperature-swing adsorption advantageously need not be cooled, since it must have a correspondingly elevated temperature for the catalytic oxidation.

[0055] The use of an appropriately designed catalytic oxidation can balance out the fluctuations in composition formed during the desorption and thus ensure a CO.sub.2 quality as uniform as possible. The control can be adapted, in such a manner, for example, that the oxygen requirement of the catalytic oxidation is taken into account and thus an oxygen concentration in the CO.sub.2 as constant as possible is always maintained, for example below 0.7% by volume, in particular below 0.6% by volume, or in particular <0.35% by volume. This control possibility is advantageous for the stability and energy efficiency of the subsequent urea plant. For control of the O.sub.2 content in the CO.sub.2, the desorption of the combustible components can be calculated in advance on account of the heating. Then, the amount of air can be set accordingly. There is also the possibility, e.g., of additionally measuring and controlling the O.sub.2 content in the CO.sub.2.

[0056] As a result, the invention permits the integration of known technologies such as, e.g., POX, ASU (cryogenic air separation), pressure-swing adsorption and temperature-swing adsorption, into one plant concept or method concept which can provide sufficient CO.sub.2 for urea synthesis, and so complete reaction of the ammonia that is manufactured is possible, wherein the required CO.sub.2 is provided at a high pressure level, and so a high-cost additional compression can he avoided.

LIST OF REFERENCE SIGNS

[0057]

TABLE-US-00001 10 Air separation 20 POX 30 Desulphurization 40 Water gas-shift reaction and cooling of the synthesis gas 50 Separating off H.sub.2 and CO.sub.2 51 Pressure-swing adsorption 52 Temperature-swing adsorption 53 CO.sub.2 purification 60 Ammonia synthesis 70 Urea synthesis A, Off-gas A E Energy for heating L Air NG Feed gas S Synthesis gas S First synthesis gas substream S Second synthesis gas substream R Shifted synthesis gas recycle V CO.sub.2 with impurities downstream of temperature-swing adsorption W Steam