Method for removing N2O and NOx from the nitric acid production process, and an installation suitable for same

Patent metadata

Field	Value
Publication number	US-9738521-B2
Application number	US-201213984921-A
Country	US
Kind code	B2
Filing date	Feb 14, 2012
Priority date	Feb 21, 2011
Publication date	Aug 22, 2017
Grant date	Aug 22, 2017

Abstract

The invention relates to a process and apparatus for preparing nitric acid by catalytic oxidation of NH 3 by means of oxygen and subsequent reaction of the NO x formed with an absorption medium in an absorption tower, which comprises a catalyst bed for N 2 O decomposition arranged in the process gas downstream of the catalytic NH 3 oxidation and upstream of the absorption tower in the flow direction and a catalyst bed for NO x reduction and effecting a further decrease in the amount of N 2 O arranged in the tailgas downstream of the absorption tower in the flow direction,
wherein the amount of N 2 O removed in the catalyst bed for N 2 O removal arranged in the process gas is not more than that which results in an N 2 O content of >100 ppmv and a molar N 2 O/NO x ratio of >0.25 before entry of the tailgas into the catalyst bed for NO x reduction and the catalyst bed for NO x reduction and effecting a further decrease in the amount of N 2 O arranged in the tailgas contains at least one iron-loaded zeolite catalyst and NH 3 is added to the tailgas before entry into the catalyst bed in such an amount that an NO x concentration of <40 ppmv results at the outlet from the catalyst bed and the operating parameters are selected in such a way that an N 2 O concentration of <200 ppmv results.

First claim

The invention claimed is:

1. A process for preparing nitric acid comprising:
catalytically oxidizing NH 3 by means of oxygen;
decomposing N 2 O in a catalyst bed arranged in the process gas stream downstream of the catalytic NH 3 oxidation and upstream of an absorption tower;
subsequently reacting the NO x formed with an absorption medium in the absorption tower; and
reducing NO x and effecting a further decrease in the amount of N 2 O in a catalyst bed arranged in the tailgas stream downstream of the absorption tower;
wherein
the tailgas entering the catalyst bed for NO x reduction and effecting a further decrease in the amount of N 2 O has an N 2 O content>100 ppmv and a molar N 2 O/NO x ratio>0.25,
the catalyst bed for NO x reduction and effecting a further decrease in the amount of N 2 O arranged in the tailgas stream contains at least one iron-loaded zeolite catalyst,
NH 3 is added to the tailgas before entry into the catalyst bed for NO x reduction and effecting a further decrease in the amount of N 2 O arranged in the tailgas stream in such an amount that an NO x concentration of <40 ppmv results at the outlet from the catalyst bed for NO x reduction and effecting a further decrease in the amount of N 2 O arranged in the tailgas stream, and
the operating parameters of pressure, temperature and space velocity are selected in such a way that an N 2 O concentration of <200 ppmv results, with the proviso that the N 2 O concentration at the outlet from the catalyst bed for NO x reduction is less than the N 2 O content entering the catalyst bed for NO x reduction.

2. The process as claimed in claim 1 , wherein a targeted setting of the N 2 O removal in the catalyst bed arranged in the process gas stream downstream of the catalytic NH 3 oxidation and upstream of the absorption tower is achieved by variation of the layer thickness or the layer height of the catalyst bed and/or selection of the catalyst material and/or selection of the geometry of the catalyst material.

3. The process as claimed in claim 1 , wherein the catalyst bed arranged in the process gas stream downstream of the catalytic NH 3 oxidation and upstream of the absorption tower contains a catalyst suitable for the decomposition of N 2 O, the catalyst containing transition metal oxides and/or transition metal-containing mixed oxides.

4. The process as claimed in claim 1 , wherein the catalyst material of the catalyst bed arranged in the process gas stream downstream of the catalytic NH 3 oxidation and upstream of the absorption tower contains cobalt-containing oxides or mixed oxides as active components.

5. The process as claimed in claim 1 , wherein the catalyst material of the catalyst bed arranged in the process gas stream downstream of the catalytic NH 3 oxidation and upstream of the absorption tower is configured as a shaped body which has the geometry of a cylinder, hollow cylinder, multi-hole cylinder, perforated and unperforated trilobes or polylobes or honeycomb structures.

6. The process as claimed in claim 1 , wherein the pressure drop over the catalyst material of the catalyst bed arranged in the process gas stream downstream of the catalytic NH 3 oxidation and upstream of the absorption tower is <30 mbar.

7. The process as claimed in claim 1 , wherein the N 2 O removal in the catalyst bed in the process gas downstream of the catalytic NH 3 oxidation and upstream of the absorption tower is 40-90%, based on the amount of N 2 O initially present.

8. The process as claimed in claim 1 , wherein the space velocity at which the tailgas is passed over the catalyst material of the catalyst bed arranged in the tailgas stream downstream of the absorption tower is from 200 to 200 000 h −1 , and the pressure in the tailgas before entry into the catalyst material of the catalyst bed arranged in the tailgas stream downstream of the absorption tower is from 1 to 50 bar, and the temperature in the tailgas before entry into the catalyst material of the catalyst bed arranged in the tailgas stream downstream of the absorption tower is from 300° C. to 600° C.

9. The process as claimed in claim 1 , wherein the operating parameters pressure, temperature and space velocity in/over the catalyst bed arranged in the tailgas stream downstream of the absorption tower are set and/or hydrocarbons are added as reducing agent for N 2 O in this catalyst bed in such a way that the decrease in the content of N 2 O in this catalyst bed is at least 50%, based on the content of N 2 O at the entry into this catalyst bed.

10. The process as claimed in claim 1 , wherein an amount of from 0.9 to 1.3 mol of NH 3 per mol of NO x to be reduced is added to the tailgas before entry into the catalyst material of the catalyst bed arranged in the tailgas stream downstream of the absorption tower.

11. The process as claimed in claim 1 , wherein hydrocarbons are mixed into the tailgas before entry into the catalyst material of the catalyst bed arranged in the tailgas stream downstream of the absorption tower, where an amount of 0.2-1 mol of hydrocarbon/1 mol of N 2 O to be reduced are added and, based on the NO x entry concentration, 1-2 mol of NH 3 /mol of NO x are added.

12. The process as claimed in claim 1 , wherein the catalyst bed for NO x reduction and effecting a further decrease in the amount of N 2 O arranged in the tailgas stream is divided into a plurality of reaction zones or physically separate reaction stages and graduated introduction of NH 3 into the individual reaction zones or into the physically separate reaction stages of the catalyst bed arranged in the tailgas stream is carried out.

13. The process as claimed in claim 1 , wherein the iron-loaded zeolite catalyst of the catalyst bed arranged in the tailgas stream contains, based on the mass of zeolite, up to 25% by weight of iron.

14. The process as claimed in claim 1 , wherein the iron-loaded zeolite catalyst of the catalyst bed arranged in the tailgas stream contains>50% by weight of an iron-loaded zeolite or a plurality of iron-loaded zeolites.

15. The process as claimed in claim 1 , wherein the iron-loaded zeolite catalyst of the catalyst bed arranged in the tailgas stream is a zeolite of the MFI, BEA, FER, MOR, FAU and/or MEL type.

16. The process as claimed in claim 1 , wherein the iron-loaded zeolite catalyst of the catalyst bed arranged in the tailgas stream comprises a zeolite whose lattice aluminum has been completely or partly isomorphously replaced by one or more elements, where the elements are selected from the group consisting of B, Be, Ga, Fe, Cr, V, As, Sb and Bi, or comprises a zeolite whose lattice silicon has been completely or partly replaced by one or more elements selected from the group consisting of Ge, Ti, Zr and Hf and/or the iron-loaded zeolite catalyst of the catalyst bed arranged in the tailgas stream comprises a zeolite which has been hydrothermally pretreated with steam, where the zeolite which has been thermally pretreated with steam has a ratio of extra-lattice aluminum to lattice aluminum of at least 1:2.

17. The process as claimed in claim 1 , wherein the gas flows axially, laterally or radially through the catalyst bed arranged in the tailgas stream downstream of the absorption tower.

18. The process as claimed in claim 1 , wherein one or more further stages for N 2 O and/or NO x removal are arranged between the catalyst bed for N 2 O decomposition arranged in the process gas stream and the catalyst bed for NO x reduction and effecting a further decrease in the amount of N 2 O arranged in the tailgas stre

Assignees

• Schwefer Meinhard
• Siefert Rolf
• Fuchs Jürgen
• Ruthardt Klaus
• Groves Michael
• Thyssenkrupp Uhde Gmbh

Inventors

• Schwefer Meinhard
• Siefert Rolf
• Fuchs Jürgen
• Ruthardt Klaus
• Groves Michael

Classifications

• C01B21/38

  Nitric acid · CPC title

• C01B21/40 Primary

  Preparation by absorption of oxides of nitrogen {(C01B21/26 takes precedence)} · CPC title

• B01J29/68

  Iron group metals or copper · CPC title

• B01J29/46

  Iron group metals or copper · CPC title

• B01D2255/504

  ZSM 5 zeolites · CPC title