Process for revamping an ammonia plant

US11097944B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11097944-B2
Application numberUS-201716078846-A
CountryUS
Kind codeB2
Filing dateFeb 6, 2017
Priority dateFeb 25, 2016
Publication dateAug 24, 2021
Grant dateAug 24, 2021

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  1. Title

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  5. First independent claim

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Abstract

Official abstract text for this publication.

A method is described for revamping an ammonia production facility said ammonia production facility having a front end comprising one or more reformers fed with a hydrocarbon feedstock at a hydrocarbon feed stock feed rate and a high-temperature shift reactor fed with a reformed gas obtained from said one or more reformers and containing a fixed bed of iron-containing water-gas shift catalyst, said front end operating at a first steam-to-carbon ratio and a first pressure drop, said method comprising the steps of (i) replacing the iron-containing water-gas shift catalyst with a low-steam water-gas shift catalyst to form a modified front end, (ii) operating the modified front end at a second steam-to-carbon ratio and a second pressure drop, wherein the second steam-to-carbon ratio is at least 0.2 less than the first steam-to-carbon ratio and the second pressure drop is less than the first pressure drop, and (iii) increasing the hydrocarbon feed stock feed rate to said one or more reformers.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for revamping an ammonia production facility, said ammonia production facility having a front end comprising: (a) one or more reformers fed with a hydrocarbon feedstock at a hydrocarbon feed stock feed rate; and (b) a high-temperature shift reactor fed with a reformed gas obtained from said one or more reformers, the high-temperature shift reactor having an inlet temperature in a range of from 300° C. to 450° C. and containing a fixed bed of iron-containing a high-temperature water-gas shift catalyst, said front end operating at a first steam-to-carbon ratio at or above 1.5 and a first pressure drop at or above 5 barg, said method comprising the steps of: (i) replacing the iron-containing high-temperature water-gas shift catalyst with a low-steam water-gas shift catalyst to form a modified front end, wherein the low steam water gas shift catalyst is an enhanced iron-containing high temperature shift catalyst that is a precipitated iron-containing catalyst with an iron oxide content, expressed as Fe 2 O 3 , of 60 to 95% by weight, having a BET surface area in the range of from 20 m 2 /g to 40 m 2 /g, or an iron-free high temperature shift catalyst comprising a zinc-aluminate spinel or oxides of zinc and aluminum and one or more promoters that is Na, K, Rb, Cs, Cu, Ti, Zr, a rare earth element or a mixture thereof, (ii) configuring the modified front end to operate at a second steam-to-carbon ratio and a second pressure drop, wherein the second steam-to-carbon ratio is at least 0.2 less than the first steam-to-carbon ratio and the second pressure drop is less than the first pressure drop, and (iii) increasing the hydrocarbon feed stock feed rate to said one or more reformers; such that the high-temperature shift reactor remains configured to operate under high-temperature water-gas shift conditions. 2. The method of claim 1 , wherein the ammonia production facility front end comprises a fired steam reformer and optionally a secondary reformer. 3. The method of claim 1 , wherein the high temperature shift reactor is operated at an inlet temperature in the range of from 310 to 380° C. and at a pressure in the range of from 1 to 100 bar abs. 4. The method of claim 1 , wherein the second steam-to-carbon ratio is at least 0.3 less than the first steam-to-carbon ratio. 5. The method of claim 1 wherein the steam to dry gas ratio at the inlet to the high temperature shift reactor is reduced to 0.45:1 or less after replacement of the iron-containing high-temperature water-gas shift catalyst with the low-steam water-gas shift catalyst. 6. The method of claim 1 , wherein the second pressure drop through the front end is at least 1 barg lower than the first pressure drop through the front end. 7. The method of claim 1 wherein the low steam water gas shift catalyst is the iron-free high temperature shift catalyst comprising the zinc-aluminate spinel or oxides of zinc and aluminum and one or more promoters that is Na, K, Rb, Cs, Cu, Ti, Zr, a rare earth element or a mixture thereof. 8. The method of claim 1 , wherein the low steam water gas shift catalyst is the enhanced iron-containing water gas shift catalyst that is the precipitated iron-containing catalyst with an iron oxide content, expressed as Fe 2 O 3 , of 60 to 95% by weight, having a BET surface area in the range of from 20 m 2 /g to 34 m 2 /g. 9. The method of claim 1 , wherein the low steam water gas shift catalyst is the enhanced iron-containing water gas shift catalyst is in the form of a cylindrical pellet having a length C and diameter D, wherein the surface of the cylindrical pellet has two or more flutes running along its length, said cylinder having domed ends of lengths A and B such that (A+B+C)/D is in the range of from 0.25 to 1.25, and (A+B)/C is in the range of from 0.03 to 0.3. 10. The method of claim 1 , wherein the low steam water gas shift catalyst is the enhanced iron-containing water gas shift catalyst comprising one or more iron oxides stabilized with chromia, acicular iron oxide particles, and one or more copper compounds. 11. The method of claim 1 , wherein the low steam water gas shift catalyst is the iron-free high temperature shift catalyst comprising the zinc-aluminate spinel. 12. The method of claim 1 , wherein the low steam water gas shift catalyst comprises a mixture of zinc alumina spinel and zinc oxide in combination with an alkali metal that is Na, K, Rb, Cs, or a mixture thereof. 13. The method of claim 1 , wherein the low steam water gas shift catalyst is the iron-free high temperature shift catalyst comprising the oxides of zinc and aluminum and one or more promoters that is Na, K, Rb, Cs, Cu, Ti, Zr, a rare earth element, or a mixture thereof. 14. The method of claim 1 , wherein the front-end pressure drop is increased by the increase in hydrocarbon feedstock feed rate in step (iii) to 90-100% of the first front-end pressure drop. 15. The method of claim 1 , wherein the second steam-to-carbon ratio is at least 0.4 less than the first steam-to-carbon ratio. 16. The method of claim 1 , wherein the steam to dry gas ratio at the inlet to the high temperature shift reactor is reduced after replacement of the iron-containing water-gas shift catalyst to ≤0.42:1. 17. The method of claim 1 , wherein the low steam water gas shift catalyst is the enhanced iron-containing water gas shift catalyst having a BET surface area in a range of from 20 m 2 /g to 34 m 2 /g.

Assignees

Inventors

Classifications

  • Cylinders or rings · CPC title

  • the reforming step being a steam reforming step · CPC title

  • followed by reaction of water vapour with carbon monoxide · CPC title

  • using catalysts, e.g. selective catalysts · CPC title

  • Ammonia synthesis · CPC title

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What does patent US11097944B2 cover?
A method is described for revamping an ammonia production facility said ammonia production facility having a front end comprising one or more reformers fed with a hydrocarbon feedstock at a hydrocarbon feed stock feed rate and a high-temperature shift reactor fed with a reformed gas obtained from said one or more reformers and containing a fixed bed of iron-containing water-gas shift catalyst, …
Who is the assignee on this patent?
Johnson Matthey Plc
What technology area does this patent fall under?
Primary CPC classification C01B3/025. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 24 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).