IP Library Granted Patent US 10,899,617
Granted Patent B2
US 10,899,617 · App. 15/667,293 · Granted Jan 26, 2021

Method for removing N

Inventors: Meinhard Schwefer (Meschede, DE); Rolf Siefert (Rheda-Wiedenbrück, DE); Jürgen Fuchs (Dortmund, DE); Klaus Ruthardt (Dortmund, DE); Michael Groves (Gevelsberg, DE)
Assignee: THYSSENKRUPP INDUSTRIAL SOLUTIONS AG
C01B21/40B01D53/869B01D53/8628B01J29/072C01B21/265C01B21/38B01D2255/2065B01D2255/20738B01D2255/20746B01D2255/20761B01D2255/502B01D2255/504B01D2257/402B01D2257/404B01J29/46B01J29/68B01J29/7615B01J2229/42Y02C20/10Y02P20/151
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Quick Facts
Patent No.
US 10,899,617
App. No.
15/667,293
Granted
Jan 26, 2021
Kind
B2
Abstract

An apparatus is provided for treatment of process gas formed during nitric acid production by catalytic oxidation of NH 3 . The apparatus includes a reactor, a first catalyst bed for N 2 O decomposition, an absorption tower to react the NO x formed with an absorption medium downstream of the first catalyst bed, a device for adding NH 3 added to tailgas entering the second catalyst bed, and a second catalyst bed for NO x reduction and further decrease in N 2 O in the tailgas exiting the absorption tower. The second catalyst bed contains at least one iron-loaded zeolite catalyst. N 2 O removal in the first catalyst bed is limited such that the process gas exiting the first catalyst bed exhibits a N 2 O content of >100 ppmv and a molar N 2 O/NO x ratio of >0.25. Treated gas exiting the second catalyst bed has a NO x concentration of <40 ppmv and a N 2 O concentration of <200 ppmv.

Claims (18)

1. A nitric acid plant in which a catalytic removal of N 2 O formed in a catalytic NH 3 oxidation is carried out in an NO x -containing process gas and a further reduction of the N 2 O content and a reduction of a NO x content is carried out in a tailgas downstream of an absorption tower, which comprises at least the following elements:

A) a reactor for the catalytic oxidation of NH 3 by means of oxygen to produce the NO x -containing process gas,

B) at least one first catalyst bed for N 2 O decomposition through which the NO x -containing process gas flows and which is arranged directly downstream from the catalytic NH 3 oxidation, in the flow direction, where the NO x -containing process gas has a temperature of 850-950° C.,

C) the absorption tower, arranged downstream from the at least one first catalyst bed, for reacting the NO x formed from the NO x -containing process gas with an absorption medium, leaving the tailgas containing NO x and N 2 O,

D) at least one device for feeding gaseous reducing agent into the tailgas leaving the absorption tower in the flow direction,

E) at least one second catalyst bed for NO x reduction and effecting a further decrease in the N 2 O content, through which the tailgas flows and which is arranged downstream of the device for feeding gaseous reducing agent into the tailgas in the flow direction, and wherein

F) the first catalyst bed (i) contains a catalyst suitable for the decomposition of N 2 O and (ii) is configured such that the NO x -containing process gas exiting the first catalyst bed exhibits a N 2 O content of >100 ppmv and a molar N 2 O/NO x ratio of >0.25, and

G) the second catalyst bed contains a catalyst containing at least one iron-loaded zeolite.

2. The nitric acid plant as claimed in claim 1 , wherein the absorption medium is water.

3. The nitric acid plant as claimed in claim 1 , wherein the catalyst material of the first catalyst bed contains transition metal oxides and/or transition metal-containing mixed oxides and/or noble metals as active components.

4. The nitric acid plant as claimed in claim 1 , wherein the catalyst material of the first catalyst bed contains transition metal mixed oxides having a perovskite structure, a perovskite-like structure, or a spinel structure.

5. The nitric acid plant as claimed in claim 1 , wherein the catalyst material of the first catalyst bed contains cobalt-containing oxides or mixed oxides as active components.

6. The nitric acid plant as claimed in claim 5 , wherein the catalyst material of the first catalyst bed comprises a porous support composed of polycrystalline or vitreous inorganic material, a cerium oxide functional layer applied thereto, and a layer of oxidic cobalt-containing material applied thereto.

7. The nitric acid plant as claimed in claim 1 , wherein the bed height of the catalyst material of the first catalyst bed is 3-30 cm.

8. The nitric acid plant as claimed in claim 7 , wherein the bed height of the catalyst material of the first catalyst bed is 5-20 cm.

9. The nitric acid plant as claimed in claim 7 , wherein the bed height of the catalyst material of the first catalyst bed is 10-20 cm.

10. The nitric acid plant as claimed in claim 1 , wherein the iron-loaded zeolite catalyst in the second catalyst bed is a zeolite of the MFI, BEA, FER, MOR, FAU and/or MEL type.

11. The nitric acid plant as claimed in claim 10 , wherein the iron-loaded zeolite catalyst in the second catalyst bed is of the MFI and/or BEA and/or FER type.

Assignments (2)
CHANGE OF NAME Recorded Apr 22, 2025
From: THYSSENKRUPP INDUSTRIAL SOLUTIONS AG
To: THYSSENKRUPP UHDE GMBH
Reel/Frame 070914/0528 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 2, 2020
From: SCHWEFER, MEINHARD; SIEFERT, ROLF; FUCHS, JÜRGEN; RUTHARDT, KLAUS; GROVES, MICHAEL
To: THYSSENKRUPP INDUSTRIAL SOLUTIONS AG
Reel/Frame 054241/0775 →
Priority Claims (2)
DE 10 2011 011 881 · Feb 21, 2011 · national
WO PCT/EP2012/000642 · Feb 14, 2012 · international
Continuity (2)
Division 13984921
Related Publication 20170334722A1 · Nov 23, 2017