Process for purifying synthesis gas by washing with aqueous solutions of amines

Patent metadata

Field	Value
Publication number	US-10118824-B2
Application number	US-201415105075-A
Country	US
Kind code	B2
Filing date	Dec 16, 2014
Priority date	Dec 17, 2013
Publication date	Nov 6, 2018
Grant date	Nov 6, 2018

Abstract

The invention relates to a process for purifying synthesis gas, comprising at least one stage for separating the crude synthesis gas to be treated into at least two effluents, namely a first part and a complementary part, in which the said first part is subjected to a carbon monoxide conversion stage with steam and the said complementary part is subjected to a COS and HCN catalytic hydrolysis stage, the two gas flows, namely the first part and complementary part, are then each treated separately in two stages intended to remove acid gases such as CO 2 and H 2 S, by washing with aqueous solutions of specific amines, before a recombination stage of the two treated effluents.

First claim

The invention claimed is:

1. A process for purification of synthesis gas, comprising at least the following stages:
a) a stage for dividing the synthesis gas into at least a first synthesis gas flow and a second synthesis gas flow of the same composition,
b1) a stage for the steam conversion of carbon monoxide of the first synthesis gas flow leaving stage a), in order to produce a stage b1) gaseous effluent containing at least hydrogen H 2 and carbon dioxide CO 2 , less than 15% volume (vol. %) of carbon monoxide CO and acid gases including H 2 S and CO 2 ,
b2) a stage for the removal of acid gases including H 2 S and CO 2 from the stage b1) gaseous effluent by contacting said stage b1) gaseous effluent with a solvent which is a first aqueous solution of amines comprising at least one secondary amine, said first aqueous solution of amines further comprising at least one tertiary amine or a sterically hindered secondary amine different from the secondary amine and containing at least one quaternary carbon atom in the α or alpha position of the nitrogen atom or two tertiary carbon atoms in the α and α′ positions, so as to remove acid gases including H 2 S and CO 2 and produce at least one stage b2) gaseous effluent containing less than 5 vol. % of carbon dioxide CO 2 , and less than 50 ppm by volume of H 2 S,
c1) a stage for catalytic hydrolysis of COS and HCN present in the second synthesis gas flow that has not undergone the conversion reaction of carbon monoxide with steam, in order to produce a stage c1) gaseous effluent containing less than 25 ppm by volume of COS, and less than 5 ppm by volume of HCN, and containing acid gases including H 2 S and CO 2 ,
c2) a stage for removal of acid gases including H 2 S and CO 2 from said stage c1) gaseous effluent by contacting said stage c1) gaseous effluent with a solvent which is a second aqueous solution of amines containing at least one tertiary amine, so as to produce at least one stage c2) gaseous effluent containing less than 10 vol. % of carbon dioxide CO 2 , and less than 50 ppmv of H 2 S, wherein the second aqueous solution of amines contains between 25 and 50 wt. % of a tertiary amine and contains between 50 and 75 wt. % of water, and
d) recombination of at least a part of said stage b2) effluent and at least part of said stage c2) to obtain a purified synthesis gas,
wherein said first aqueous solution of amines and said second aqueous solution of amines are different.

2. The process according to claim 1 , wherein stage b1) is carried out at an absolute pressure between 20 and 120 bar, at a gas hourly space velocity between 1,000 and 10,000 h 1 , and at a temperature between 150 and 550° C.

3. The process according to claim 1 , wherein stage b1) is conducted in the presence of a catalyst containing at least one element from group VIII and/or at least one element from group VIB of the Periodic Table, and a support chosen from aluminas, silica, and silica-aluminas.

4. The process according to claim 1 , wherein said stage b1) gaseous effluent is routed to a stage b1′) for catalytic hydrolysis of COS and HCN to H 2 S and NH 3 to obtain a stage b1′) gaseous effluent which is sent to said stage b2).

5. The process according to claim 1 , wherein the secondary amine or amines used in stage b2) are chosen from diethanolamine, diisopropanolamine, piperazine and derivatives thereof containing at least a non substituted nitrogen atom, morpholine and non N-substituted derivatives thereof, piperidine and non N-substituted derivatives thereof, N-(2′-hydroxyethyl)-2-amino-2-methyl-1-propanol, N-(2′-hydroxypropyl)-2-amino-2-methyl-1-propanol, and N-(2′-hydroxybutyl)-2-amino-2-methyl-1-propanol, individually or as a mixture.

6. The process according to claim 1 , wherein said stage b2) is carried out in the presence of an aqueous solution of amines containing at least one secondary amine, mixed with at least one tertiary amine, wherein said tertiary amine or amines are chosen from methyldiethanolamine, triethanolamine, ethyldiethanolamine, diethylethanolamine, dimethylethanolamine, 1-methyl-4-(3-dimethylaminopropyl)-piperazine, 1-ethyl-4-(diethylaminoethyl)-piperazine, 1-methyl-4-hydroxy-piperidine, 1-methyl-2-hydroxymethyl-piperidine, tert-butyldiethanolamine, 1,2-bis-(2-dimethylaminoethoxy)-ethane bis(dimethylamino-3-propyl)ether, bis(diethylamino-3-propyl)ether, (dimethylamino-2-ethyl)-(dimethylamino-3-propyl)-ether, (diethylamino-2-ethyl)-(dimethylamino-3-propyl)-ether, (dimethylamino-2-ethyl)-(diethylamino-3-propyl)-ether, (diethylamino-2-ethyl)-(diethylamino-3-propyl)-ether, N-methyl-N-(3-methoxypropyl)-2-aminoethanol, N-methyl-N-(3-methoxypropyl)-1-amino-2-propanol, N-methyl-N-(3-methoxypropyl)-1-amino-2-butanol, N-ethyl-N-(3-methoxypropyl)-2-aminoethanol, N-ethyl-N-(3-methoxypropyl)-1-amino-2-propanol, N-ethyl-N-(3-methoxypropyl)-1-amino-2-butanol, N-isopropyl-N-(3-methoxypropyl)-2-aminoethanol, N-isopropyl-N-(3-methoxypropyl)-1-amino-2-propanol, N-isopropyl-N-(3-methoxypropyl)-1-amino-2-butanol, 1-(4-morpholino)-2-(methylisopropylamino)-ethane, 1-(4-morpholino)-2-(methyltertiobutylamino)-ethane, 1-(4-morpholino)-2-(diisopropylamino)-ethane, and 1-(4-morpholino)-2-(1-piperidinyl)-ethane, individually or as a mixture.

7. The process according to claim 1 , wherein stage b2) is carried out in the presence of an aqueous solution of amines containing at least one secondary amine, mixed with at least one sterically hindered secondary amine containing at least one quaternary carbon atom in the α or alpha position of the nitrogen atom, or two tertiary carbon atoms in the α and α′ position, and wherein the sterically hindered secondary amine or amines are chosen from N-(2′-hydroxyethyl)-2-amino-2-methyl-1-propanol, N-(2′-hydroxypropyl)-2-amino-2-methyl-1-propanol, N-(2′-hydroxybutyl)-2-amino-2-methyl-1-propanol.

8. The process according to claim 1 , wherein stage b2) is carried out in the presence of an aqueous solution of amines containing at least one secondary amine, mixed with at least one tertiary amine or a sterically hindered secondary amine containing at least one quaternary carbon atom in the α or alpha position of the nitrogen atom or two tertiary carbon atoms in the α and α′ position, and wherein said primary and/or secondary amines are selected from diethanolamine, N-butylethanolamine, piperazine, 1-methylpiperazine, 2-methylpiperazine, N-(2-hydroxyethyl)piperazine, N-(2-aminoethyl)piperazine, morpholine, 3-(methylamino)propylamine, and 1,6-hexanediamine and N-alkylated derivatives thereof, individually or as a mixture.

9. The process according to claim 1 , wherein stage c1) is carried out in the presence of a catalyst containing a compound based on platinum, or an oxide of an element selected from titanium, zirconium, aluminium, chromium and zinc, individually or as a mixture, said stage c1) being carried out at a temperature between 100 and 400° C., and at an absolute pressure between 20 and 120 bar.

10. The process according to claim 1 , wherein the tertiary amine or amines used in the stage c2) are chosen from methyldiethanolamine, triethanolamine, ethyldiethanolamine, diethylethanolamine, dimethylethanolamine, 1-methyl-4-(3-dimethylaminopropyl)-piperazine, 1-ethyl-4-(diethylaminoethyl)-piperazine, 1-methyl-4-hydroxy-piperidine, 1-methyl-2-hydroxymethyl-piperidine, tert-butyldiethanolamine, 1,2-bis-(2-dimethylaminoethoxy)-ethane, bis(dimethylamino-3-propyl)ether, bis(diethylamino-3-propyl)ether, (dimethylamino-2-ethyl)-(dimethylamino-3-propyl)-ether, (diethylamino-2-ethyl)-(dimethylamino-3-propyl)-ether, (dimethylamino-2-ethyl)-(diethylamino-3-propyl)-ether, (diethylamino-2-ethyl)-(diethylamino-3-propyl)-ether, N-methyl-N-(3-methoxypropyl)-2-aminoethanol, N-methyl-N-(3-methoxyprop

Assignees

• Sofiproteol
• Axens
• Ifp Energies Now
• Bionext
• Thyssenkrupp Ind Solutions Ag
• Total Raffinage Chimie
• Commissariat Energie Atomique
• Avril

Inventors

• Chiche David
• Pierron Anne Claire
• Ullrich Norbert

Classifications

• C01B3/16 Primary

  using catalysts · CPC title

• C01B2203/1047

  Group VIII metal catalysts · CPC title

• C01B2203/0465

  Composition of the impurity · CPC title

• C01B2203/06

  Integration with other chemical processes · CPC title

• C01B2203/1041

  Composition of the catalyst · CPC title