IP Library Granted Patent US 10,434,456
Granted Patent B2
US 10,434,456 · App. 15/525,498 · Granted Oct 8, 2019

Process for removing and recovering H

Inventors: Hendricus Adrianus Johannes Van Dijk (Petten, NL); Paul Dean Cobden (Petten, NL); Stéphane Walspurger (Petten, NL)
Assignee: STICHTING ENERGIEONDERZOEK CENTRUM NEDERLAND
B01D53/02B01D53/526B01D53/62B01D53/8603B01J20/08B01J20/3466C01B17/0404B01D2251/30B01D2253/104B01D2253/25B01D2255/202B01D2255/2022B01D2255/2092B01D2257/30B01D2257/304B01D2257/308B01D2257/504B01D2258/05B01D2259/40086Y02C10/04Y02C10/08Y02P20/152
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Quick Facts
Patent No.
US 10,434,456
App. No.
15/525,498
Granted
Oct 8, 2019
Kind
B2
Abstract

A process for altering the composition of a feed gas containing H 2 S equivalents is disclosed. The process comprises (a) contacting the feed gas with a solid adsorbent at a temperature of 250-500° C., to obtain a loaded adsorbent, (b) purging the loaded adsorbent with a purge gas comprising steam, thus producing a product stream which typically contains substantially equal levels of CO 2 and H 2 S. The process further comprises a step (c) of regenerating the purged adsorbent by removal of water. The adsorbent comprises alumina and one or more alkali metals, such as potassium oxides, hydroxide or the like.

Claims (83)

1. A process for altering the composition of a gas comprising H 2 S equivalents and CO2, comprising the steps of:

(a) contacting a feed gas containing H 2 S equivalents, CO 2 and optionally H 2 O, wherein the molar ratio of H 2 O to H 2 S equivalents is within the range of 0-(5+X), with a solid adsorbent at a temperature of 250-500° C., to obtain a loaded adsorbent and a first product gas;

(b) contacting the loaded adsorbent with a purge gas containing H 2 O, to obtain a second product gas; and

(c) regenerating the adsorbent after step (b) by removal of H 2 O,

wherein the process is performed in cycles of steps (a) to (c), and wherein the feed gas and/or the purge gas contains a reducing agent and the adsorbent comprises alumina and one or more alkali metals, and wherein X is defined as:

X

=

n

i

[

H

2

S

equivalent

]

i

[

H

2

S

equivalents

]

wherein [H 2 S equivalents] indicates the total concentration of H 2 S equivalents, [H 2 S equivalent] i indicates the concentration of a particular H 2 S equivalent i and n i indicates the amount of water molecules n consumed when said H 2 S equivalent i is converted to H 2 S.

2. The process according to claim 1 , wherein the H 2 S equivalents comprise H 2 S, COS and/or CS 2 .

3. The process according to claim 1 , wherein the molar ratio of H 2 S equivalents to CO 2 in the feed gas is below 1.

4. The process according to claim 1 , wherein the molar ratio of H 2 S equivalents to CO 2 in the feed gas is in the range of 0.001-0.1.

5. The process according to claim 1 , wherein the feed gas contains 0.1-20% H 2 as the reducing agent.

6. The process according to claim 1 , wherein the adsorbent further comprises one or more divalent metals.

7. The process according to claim 1 , wherein the divalent metals are oxides, hydroxides, carbonates, sulphides and/or hydrosulphides.

8. The process according to claim 1 , wherein the adsorbent further comprises MgO.

9. The process according to claim 5 , wherein the alkali metal is K and the adsorbent is K-promoted alumina, or is based on a K-promoted hydrotalcite.

10. The process according to claim 1 , wherein the process is continued with step (a) after the regeneration of step (c).

11. The process according to claim 1 , wherein step (b) is performed counter-currently with respect to step (a).

12. The process according to claim 1 , wherein the purge gas comprises at least 75% H 2 O.

13. The process according to claim 1 , wherein the first product gas contains less than 10 ppm of H 2 S equivalents, and/or the first product gas contains less than 0.1 times the level of H 2 S equivalents of the feed gas, and/or the first product gas has a molar ratio of H 2 S equivalents to CO 2 of less than 0.005.

14. The process according to claim 1 , wherein the second product gas has a molar ratio of H 2 S equivalents to CO 2 of at least 0.5.

15. The process according to claim 1 , wherein the feed gas is an optionally pre-dried syngas further containing H 2 and CO.

16. The process according to claim 1 , wherein the feed gas is an optionally pre-treated Claus tail gas further containing N 2 .

17. The process according to claim 1 , wherein the second product gas is subjected, optionally after pre-drying, to a Claus process to obtain elemental sulphur and a tail gas comprising H 2 S equivalents and CO 2 , and the tail gas is used as feed gas in step (a), optionally after pre-drying.

18. A method for the production of elemental sulphur comprising subjecting a H 2 S-enriched gas to a Claus process, wherein the H 2 S-enriched gas is obtained in step (b) of a process for altering the composition of a gas comprising H 2 S equivalents and CO 2 , comprising the steps of:

(a) contacting a feed gas containing H 2 S equivalents, CO 2 and optionally H 2 O, wherein the molar ratio of H 2 O to H 2 S equivalents is within the range of 0-(5+X), with a solid adsorbent at a temperature of 250-500° C., to obtain a loaded adsorbent and a first product gas;

(b) contacting the loaded adsorbent with a purge gas containing H 2 O, to obtain a second product gas; and

(c) regenerating the adsorbent after step (b) by removal of H 2 O,

wherein the process is performed in cycles of steps (a) to (c), and wherein the feed gas and/or the purge gas contains a reducing agent and the adsorbent comprises alumina and one or more alkali metals, and wherein X is defined as:

X

=

n

i

[

H

2

S

equivalent

]

i

[

H

2

S

equivalents

]

wherein [H 2 S equivalents] indicates the total concentration of H 2 S equivalents, [H 2 S equivalent] i indicates the concentration of a particular H 2 S equivalent i and n i indicates the amount of water molecules n consumed when said H 2 S equivalent i is converted to H 2 S.

19. The process according to claim 3 , wherein the molar ratio of H 2 S equivalents to CO 2 in the feed gas is in the range of 0.001-0.1.

20. The process according to claim 6 , wherein the divalent metals are in the form of oxides, hydroxides, carbonates, sulphides and/or hydrosulphides.

21. The process according to claim 20 , wherein the adsorbent further comprises MgO.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2020
From: STICHTING ENERGIEONDERZOEK CENTRUM NEDERLAND
To: NEDERLANDSE ORGANISATIE VOOR TOEGEPAST-NATUURWETENSCHAPPELIJK ONDERZOEK TNO
Reel/Frame 052600/0179 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 7, 2017
From: VAN DIJK, HENDRICUS ADRIANUS JOHANNES; COBDEN, PAUL DEAN; WALSPURGER, STÉPHANE
To: STICHTING ENERGIEONDERZOEK CENTRUM NEDERLAND
Reel/Frame 043214/0700 →
Priority Claims (1)
NL 2013759 · Nov 10, 2014 · national
Continuity (1)
Related Publication 20170333826A1 · Nov 23, 2017