Process for removing carbon dioxide containing acidic gases from gaseous mixtures using a basic salt activated with a hindered amine

Claim 2

In a process for removing CO 2 from gaseous feeds containing CO 2 , which comprises: (1) contacting said gaseous feeds with an aqueous scrubbing solution comprising: (a) an alkaline material comprising a basic alkali metal salt or alkali metal hydroxide, (b) an activator for said basic alkali metal salt or alkali metal hydroxide comprising at least one amine activator for said alkaline material, and (c) water, and (2) regenerating said aqueous scrubbing solution at conditions whereby CO 2 is desorbed from said aqueous scrubbing solution, the improvement which comprises providing at least one sterically hindered amine as at least one of the amine activators, and operating said process at conditions whereby the difference between the moles of carbon dioxide absorbed at the end of step (1) (absorption step) and the moles of carbon dioxide absorbed at the end of step (2) (desorption step) would be greater at the thermodynamic equilibrium (as determined from the vapor-liquid equilibrium isotherm of the reaction mixture) than in an aqueous scrubbing process wherein diethanolamine is the only amine activator utilized under similar conditions of gaseous feed composition, scrubbing solution composition, temperatures and pressures.

Claim 3

The process of claim 1 wherein the alkaline material is selected from the group consisting of potassium or sodium borate, carbonate, hydroxide, phosphate and bicarbonate.

Claim 4

The process of claim 2 wherein the alkaline material is potassium carbonate.

Claim 5

The process of claim 1 wherein the alkaline material is present in said aqueous scrubbing solution in an amount ranging from about 10 to about 40 weight percent, based on the total weight of the scrubbing solution.

Claim 6

The process of claim 1 wherein the sterically hindered amine activator is defined as a compound containing at least one secondary amino group attached to either a secondary or tertiary carbon atom or a compound containing a primary amino group attached to a tertiary carbon atom.

Claim 7

The process of claim 5 wherein the sterically hindered amine activator is selected from the group consisting of aminoethers, aminoalcohols, di- and triamines.

Claim 8

The process of claim 5 wherein the sterically hindered amine activator is selected from the group consisting of: N 1 -tert. butyl-1,4-pentanediamine; N 2 -isopropyl-4-methyl-2,4-pentanediamine; N 1 -isopropyl-2-methyl-1,2-butanediamine; 2-ethylamino-2-methyl-4-aminopentane; N-tert. pentyl-1,4-butanediamine; N-tert. butyl-1,5-pentanediamine; N 2 -isopropyl-2-methyl-1,2-propanediamine; N-sec. butyl-1,3-propanediamine; N 1 -dimethyl-1,2-diamino-2-methylbutane; N-t-butyl-ethylenediamine; N-t-butyl-1,3-propanediamine; 2-methylamino-2-methyl-4-amino pentane; N 1 -t-butyl-2-methyl-1,2-propanediamine; N 1 -butyl-2-methyl-1,2-propanediamine; N-sec. butyl-2-methyl-1,3-propanediamine; N 1 -propyl-2-methyl-1,2-propanediamine; N 1 -sec. butyl-2-methyl-1,2-propanediamine; N-t-butyl-1,4-butanediamine; N 2 -ethyl-1,2-hexanediamine; 1-methyl-1-phenyl ethylenediamine; 2-benzyl-1,2-propanediamine; 1-phenyl-1(2-amino-ethylamino)-propane; N 1 -methyl-2-phenyl-1,2-butanediamine; N 1 -cyclohexyl-1,2-propanediamine; 1-amino-1-(2-amino-isopropyl)-cyclohexane; 1-methylamino-1-aminomethyl-cyclopentane; 1-amino-1-aminomethylcycloheptane; N-isopropyl-1,2-diaminocyclohexane; N 2 -cyclohexyl-1,2-butanediamine; N 2 -cyclohexyl-1,2-propanediamine; N-cycloheptyl-ethylenediamine; N 1 -cyclohexyl-2-methyl-1,2-propanediamine; 1-(2-aminoisopropyl)-2-amino-3-methylcyclopentane; N-isopropyl-1,4-diaminocyclohexane; N 1 -cyclohexyl-N 2 -methyl-ethylenediamine; N-cyclohexyl-ethylenediamine; N 1 -cyclohexyl-N 2 -ethyl-ethylenediamine; N 1 -cyclohexyl-N 2 -methyl-1,2-propanediamine; N-cyclohexyl-1,3-propanediamine; 1,8-p-menthanediamine; 1-amino-1-aminomethylcyclohexane; 1,3-diamino-1-methylcyclohexane; N 2 -cyclohexyl-2-methyl-1,2-propanediamine; 2,4-diamino-2-methylpentane; 3,5-diamino-3-methylheptane; N 1 -tert. butyl-N 2 -isopropyl-1,3-propanediamine; N 1 -tert. butyl-N 2 -sec. butyl-ethylenediamine; N 1 -tert. butyl-N 2 -isopropyl-1,3-propanediamine; N 1 -tert. butyl-N 2 -butyl-ethylenediamine; N 1 -tert. butyl-N 2 -isobutyl-ethylenediamine; N 1 ,n 2 -diisopropyl-1,2-propanediamine; N 1 -tert. butyl-N 2 -isopropyl-ethylenediamine; N 1 -sec. butyl-N 2 -isopropyl-ethylenediamine; N 1 -tert. pentyl-N 2 -isopropyl-ethylenediamine; N 1 ,n 3 -diethyl-1,3-butanediamine; N 1 -tert. butyl-N 2 -methyl-ethylenediamine; N 1 -(2-pentyl)-N 2 -methyl-ethylenediamine; N 1 -tert. butyl-N 2 -methyl-1,4-butanediamine; N 1 -tert. butyl-N 2 -ethyl-1,3-propanediamine; N 1 -tert. butyl-N 2 ,N 2 -diethyl ethylenediamine N 1 -cyclohexyl-dipropylene triamine; N 1 ,n 3 , 2-pentamethyl-1,2,3-triaminopropane; N 1 -isopropyl-N 2 -(3-aminopropyl)-2-methyl-1,2-propanediamine;

Claim 9

2-dimethyl-diethylenetriamine; N 1 -tert. butyl-1,2,3-triaminopropane; 2,2,5,5-tetramethyldiethylenetriamine; 1-amino-1-aminomethyl-2-hydroxymethylcyclohexane; N-hydroxyethyl-1,2-diaminocyclohexane; N-cyclohexyl-1,3-diamino-2-propanol; N-(2-hydroxycyclohexyl)-1,3-propanediamine; N-isopropanol-1,2-diaminocyclohexane; N-(2-hydroxybutyl)-1,4-diaminocyclohexane; N 1 (1-hydroxy-2-butyl)-2-methyl-1,2-propanediamine; N(1-hydroxy-2-methyl-2-butyl)-1,3-propanediamine; N 1 (1,1-dimethyl-2-hydroxyethyl)-2-methyl-1,2-propanediamine; N 3 -isobutyl-2-methyl-2,3-diamino-1-propanol; N(3-hydroxy-2-butyl)-2,3-diaminobutane; N 1 -hydroxyethyl-2-methyl-1,2-propanediamine; 2,N 3 ,N 3 -trimethyl-2,3-diamino-1-propanol; N 1 ,2-dimethyl-N 1 -hydroxyethyl-1,2-propanediamine; N(1,1-dimethyl-2-hydroxyethyl)-1,3-propanediamine; N-tert. butyl-1,3-diamino-2-propanol; 3-amino-3-methyl-2-pentanol; 1-hydroxymethyl-cyclopentylamine; 2,3-dimethyl-3-amino-1-butanol; 2-amino-2-ethyl-1-butanol; 1-methyl-2-hydroxycyclopentylamine; 2-amino-2-methyl-3-pentanol; 2,4-dimethyl-2-amino cyclohexanol; 1-hydroxyethyl cyclohexylamine; 1-hydroxymethyl-3-methyl cyclohexylamine; 2-hydroxymethyl-1-methyl-cyclohexylamine; 2-amino-2-methyl-1-propanol; 2-amino-2-methyl-1-butanol; 3-amino-3-methyl-1-butanol; 3-amino-3-methyl-2-butanol; 2-amino-2,3-dimethyl-3-butanol; 2-amino-2,3-dimethyl-1-butanol; 1-hydroxymethylcyclohexylamine; 2(2-amino-2-methylpropoxy)-ethanol; 2-piperidine methanol; 2-piperidine ethanol; 2-(1-hydroxyethyl)-piperidine; 5-hydroxy-2-methyl piperidine; 2-methyl-3-hydroxy piperidine; 2,6-dimethyl-3-hydroxy piperidine; 2,5-dimethyl-4-hydroxy piperidine; 2-tert. butylamino-methyl-1,4-dimethyl-piperazine; 1-tert. butylamino-3,6-dimethyl-3,6-diaza-cycloheptane; and N-cyclohexyl-beta-alanine.

Claim 10

2-dimethyl-diethylenetriamine; N 1 -tert. butyl-1,2,3-triaminopropane; 2,2,5,5-tetramethyldiethylenetriamine; 1-amino-1-aminomethyl-2-hydroxymethylcyclohexane; N-hydroxyethyl-1,2-diaminocyclohexane; N-cyclohexyl-1,3-diamino-2-propanol; N-(2-hydroxycyclohexyl)-1,3-propanediamine; N-isopropanol-1,2-diaminocyclohexane; N-(2-hydroxybutyl)-1,4-diaminocyclohexane; N 1 (1-hydroxy-2-butyl)-2-methyl-1,2-propanediamine; N(1-hydroxy-2-methyl-2-butyl)-1,3-propanediamine; N 1 (1,1-dimethyl-2-hydroxyethyl)-2-methyl-1,2-propanediamine; N 3 -isobutyl-2-methyl-2,3-diamino-1-propanol; N(3-hydroxy-2-butyl)-2,3-diaminobutane; N 1 -hydroxyethyl-2-methyl-1,2-propanediamine; 2,N 3 ,N 3 -trimethyl-2,3-diamino-1-propanol; N 1 ,2-dimethyl-N 1 -hydroxyethyl-1,2-propanediamine; N(1,1-dimethyl-2-hydroxyethyl)-1,3-propanediamine; N-tert. butyl-1,3-diamino-2-propanol; 3-amino-3-methyl-2-pentanol; 1-hydroxymethyl-cyclopentylamine; 2,3-dimethyl-3-amino-1-butanol; 2-amino-2-ethyl-1-butanol; 1-methyl-2-hydroxycyclopentylamine; 2-amino-2-methyl-3-pentanol; 2,4-dimethyl-2-amino cyclohexanol; 1-hydroxyethyl cyclohexylamine; 1-hydroxymethyl-3-methyl cyclohexylamine; 2-hydroxymethyl-1-methyl-cyclohexylamine; 2-amino-2-methyl-1-propanol; 2-amino-2-methyl-1-butanol; 3-amino-3-methyl-1-butanol; 3-amino-3-methyl-2-butanol; 2-amino-2,3-dimethyl-3-butanol; 2-amino-2,3-dimethyl-1-butanol; 1-hydroxymethylcyclohexylamine; 2(2-amino-2-methylpropoxy)-ethanol; 2-piperidine methanol; 2-piperidine ethanol; 2-(1-hydroxyethyl)-piperidine; 5-hydroxy-2-methyl piperidine; 2-methyl-3-hydroxy piperidine; 2,6-dimethyl-3-hydroxy piperidine; 2,5-dimethyl-4-hydroxy piperidine; 2-tert. butylamino-methyl-1,4-dimethyl-piperazine; 1-tert. butylamino-3,6-dimethyl-3,6-diaza-cycloheptane; and N-cyclohexyl-beta-alanine.

Claim 11

The process of claim 5 wherein the sterically hindered amine activator is selected from the group consisting of: N-cyclohexyl-1,3-propane-diamine; 1,8-p-menthane-diamine; 1,7-bis-sec-butyl-diethylenetriamine; 2,2,5,5-tetramethyl diethylenetriamine; 3-amino-3-methyl-1-butanol; 2-amino-2-methyl-1-propanol; N 1 -isopropyl-2-methyl-1,2-propane diamine; N 1 -(1,1-dimethyl-2-hydroxyethyl)-2-methyl-1,2-propanediamine; and N 1 -isopropyl-N 2 -(3-aminopropyl)-2-methyl-1,2-propanediamine.

Claim 12

The process of claim 5 wherein said sterically hindered amine is N-cyclohexyl-1,3-propanediamine.

Claim 13

The process of claim 1 wherein said scrubbing solution additionally includes an additive selected from the antifoaming agents, antioxidants, corrosion inhibitors and mixtures thereof.

Claim 14

The process of claim 1 wherein the scrubbing solution which has been desorbed in reused to absorb a feed containing CO 2 .

Claim 15

A process for removing CO 2 from gaseous feeds containing CO 2 which comprises contacting said feed with an aqueous solution comprising (a) potassium carbonate in an amount ranging from about 10 to about 40 weight percent, (b) at least about 2 weight percent of an amine activator comprising a sterically hindered amine selected from the group consisting of: N-cyclohexyl-1,3-propanediamine; 1,8-menthanediamine; 1,7-bis-sec-butyl-diethylenetriamine; 2,2,5,5-tetramethyl diethylenetriamine; 3-amino-3-methyl-1-butanol; 2-amino-2-methyl-1-propanol, N 1 -isopropyl-2-methyl-1,2-propanediamine; N 1 (1,1-dimethyl-2-hydroxyethyl)-2-methyl-1,2-propanediamine; and N 1 -isopropyl-N 2 -(3-aminopropyl)-2-methyl-1,2-propanediamine.

Claim 16

A process for removing CO 2 from gaseous feeds containing CO 2 which comprises contacting said feed with an aqueous solution comprising (a) potassium carbonate in an amount ranging from about 10 to about 40 weight percent, (b) at least about 2 weight percent of an amine activator comprising a sterically hindered amine selected from the group consisting of: N-cyclohexyl-1,3-propanediamine; 1,8-menthanediamine; 1,7-bis-sec-butyl-diethylenetriamine; 2,2,5,5-tetramethyl diethylenetriamine; 3-amino-3-methyl-1-butanol; 2-amino-2-methyl-1-propanol, N 1 -isopropyl-2-methyl-1,2-propanediamine; N 1 (1,1-dimethyl-2-hydroxyethyl)-2-methyl-1,2-propanediamine; and N 1 -isopropyl-N 2 -(3-aminopropyl)-2-methyl-1,2-propanediamine.

Claim 17

The process of claim 12 wherein said contacting takes place at a temperature ranging from about 35 to about 150° C. and at a pressure ranging from about 100 to 500 psig for a period of from 0.1 to about 60 minutes.

Claim 18

The process of claim 12 wherein said scrubbing solution is regenerated at a temperature ranging from about 100° to 160° C. and at a pressure ranging from about 2 to about 75 psia. is reduced to a capacity of less than 25%.

Claim 19

A process for removing CO 2 from gaseous feeds containing CO 2 which comprises contacting said feed with an aqueous solution comprising: (a) potassium carbonate in an amount ranging from about 10 to about 40 weight percent, (b) at least 2 weight percent of an amine activator comprising N-cyclohexyl-1,3-propanediamine and (c) water.

Claim 20

A process for removing CO 2 from gaseous feeds containing CO 2 which comprises contacting said feed with an aqueous solution comprising: (a) potassium carbonate in an amount ranging from about 10 to about 40 weight percent, (b) at least 2 weight percent of an amine activator comprising N-cyclohexyl-1,3-propanediamine and (c) water.

Claim 21

The process of claim 15 wherein said aqueous scrubbing solution additionally includes an additive selected from the group consisting of antifoaming agents, antioxidants, corrosion inhibitors and mixtures thereof.

Claim 22

The process of claim 12 wherein said aqueous scrubbing solution includes a sterically nonhindered amine.

Claim 23

In a process for removing carbon dioxide from gaseous feeds containing carbon dioxide which comprises, in sequential steps: (1) contacting said feed with an aqueous scrubbing solution comprising: (a) an alkaline material comprising a basic alkali metal salt or alkali metal hydroxide in an amount ranging from about 10 to about 40 weight percent, (b) at least 2 weight percent of an amine activator, and (c) water, at conditions whereby said carbon dioxide is absorbed in said scrubbing solution, and (2) regenerating said scrubbing solution at conditions whereby carbon dioxide is desorbed from said scrubbing solution, the improvement which comprises providing a sterically hindered amine as an amine activator, and operating said process at conditions whereby the difference between the moles of carbon dioxide absorbed at the end of step (1)(absorption step) and the moles of carbon dioxide absorbed at the end of step (2)(desorption step) would be greater at the thermodynamic equilibrium (as determined from the vapor-liquid equilibrium isotherm of the reaction mixture) than in an aqueous scrubbing process wherein diethanolamine or 1,6-hexanediamine is the only amine activator utilized under similar conditions of gaseous feed composition, scrubbing solution composition, temperatures and pressures.

Claim 24

In a process for removing carbon dioxide from gaseous feeds containing carbon dioxide which comprises, in sequential steps: (1) contacting said feed with an aqueous scrubbing solution comprising: (a) an alkaline material comprising a basic alkali metal salt or alkali metal hydroxide in an amount ranging from about 10 to about 40 weight percent, (b) at least 2 weight percent of an amine activator, and (c) water, at conditions whereby said carbon dioxide is absorbed in said scrubbing solution, and (2) regenerating said scrubbing solution at conditions whereby carbon dioxide is desorbed from said scrubbing solution, the improvement which comprises providing a sterically hindered amine as an amine activator, and operating said process at conditions whereby the difference between the moles of carbon dioxide absorbed at the end of step (1)(absorption step) and the moles of carbon dioxide absorbed at the end of step (2)(desorption step) would be greater at the thermodynamic equilibrium (as determined from the vapor-liquid equilibrium isotherm of the reaction mixture) than in an aqueous scrubbing process wherein diethanolamine or 1,6-hexanediamine is the only amine activator utilized under similar conditions of gaseous feed composition, scrubbing solution composition, temperatures and pressures.

Claim 25

The process of claim 18 wherein said alkaline material is selected from the group consisting of potassium or sodium borate, carbonate, hydroxide, phosphate and bicarbonate.

Claim 26

The process of claim 19 wherein said alkaline material is potassium carbonate.

Claim 27

The process of claim 18 wherein the sterically hindered amine activator is defined as a compound containing at least one secondary amino group attached to either a secondary or tertiary carbon atom or a compound containing a primary amino group attached to a tertiary carbon atom.

Claim 28

The process of claim 21 wherein the sterically hindered amine activator is selected from the group consisting of aminoethers, aminoalcohols, di- and triamines.

Claim 29

The process of claim 22 wherein the sterically hindered amine activator is selected from the group consisting of: N-cyclohexyl-1,3-propanediamine; 1,8-p-menthanediamine; 1,7-bis-sec-butyl-diethylenetriamine; 2,2,5,5-tetramethyl diethylenetriamine; 3-amino-3-methyl-1-butanol; 2-amino-2-methyl-1-propanol; N 1 -isopropyl-2-methyl-1,2-propanediamine; N 1 -(1,1-dimethyl-2-hydroxyethyl)-2-methyl-1,2-propanediamine; and N 1 -isopropyl-N 2 -(3-aminopropyl)-2-methyl-1,2-propanediamine.

Claim 30

The process of claim 22 wherein the sterically hindered amine activator is N-cyclohexyl-1,3-propanediamine.

Claim 31

The process of claim 18 wherein the process is operated at conditions whereby the difference between the moles of carbon dioxide absorbed at the end of step (1)(absorption step) and the moles of carbon dioxide absorbed at the end of step (2)(desorption step) would be at least 15% greater at the thermodynamic equilibrium (as determined from the vapor liquid equilibrium isotherm of the scrubbing solution) than in an aqueous scrubbing process wherein diethanolamine or 1,6-hexanediamine is the only amine activator utilized under similar conditions of gaseous feed composition, scrubbing solution composition, temperatures and pressures.

Claim 32

The process of claim 18 wherein said scrubbing solution additionally includes an additive selected from the group consisting of antifoaming agents, antioxidants, corrosion inhibitors and mixtures thereof.

Claim 33

The process of claim 18 wherein the scrubbing solution from step (2) which has been desorbed in reused to absorb a feed containing carbon dioxide.

Claim 34

The process of claim 18 wherein said contacting in step (1)(absorption step) takes place at a temperature ranging from about 25° to about 200° C. and at a pressure ranging from about 5 to about 2000 psig for a period ranging from 0.1 to 60 minutes.

Claim 35

The process of claim 18 wherein the scrubbing solution is regenerated at a temperature ranging from 25° to 200° C. and at a pressure ranging from about 16 to about 100 psia.

Claim 36

The process of claim 1 wherein said gaseous feed contains CO 2 in combination with H 2 S.

Claim 37

The process of claim 6 wherein said sterically hindered amine is selected from the group consisting of monoprimary aliphatic diamines; arylaliphatic diamines in which the amino groups are separated by up to 5 or more than 6 carbon atoms; cycloaliphatic diamines; biprimary aliphatic diamines in which the nitrogen atoms are separated by up to 5 or more than 6 carbon atoms; disecondary aliphatic diamines; secondary-tertiary diamines; cycloaliphatic triamines; aliphatic triamines containing at most one primary amino group; biprimary or triprimary aliphatic triamines in which any two vicinal groups are separated by up to 5 or more than 6 carbon atoms; cycloaliphatic diaminoalcohols; diaminoalcohols-containing at most one primary amino group; sterically hindered primary monoaminoalcohols; sterically hindered amino-hydroxyalkylethers; 2-substituted piperidines; piperazine derivatives; azacyclo alkanes; and aminoacids.

Claim 38

The process of claim 6 wherein said sterically hindered amine is a cycloaliphatic diamine.

Claim 39

In a process for removing CO 2 from gaseous feeds containing CO 2 which comprises, in sequential steps: (1) contacting said feed with an aqueous scrubbing solution comprising (a) from about 20 to about 35 weight percent of potassium carbonate, (b) from about 2 to about 20 weight percent of an amine activator, and (c) water, at conditions whereby said CO 2 is absorbed in said scrubbing solution; (2) regenerating said scrubbing solution at conditions whereby carbon dioxide is desorbed from said scrubbing solution, the improvement which comprises providing an asymmetrical sterically hindered cycloaliphatic diamine as an amine activator wherein the sterically hindered cycloaliphatic diamine is defined as a compound having a boiling point of at least 80° C. and containing at least one secondary amino group attached to a secondary carbon atom.

Claim 40

In a process for removing CO 2 from gaseous feeds containing CO 2 which comprises, in sequential steps: (1) contacting said feed with an aqueous scrubbing solution comprising (a) from about 20 to about 35 weight percent of potassium carbonate, (b) from about 2 to about 20 weight percent of an amine activator, and (c) water, at conditions whereby said CO 2 is absorbed in said scrubbing solution; (2) regenerating said scrubbing solution at conditions whereby carbon dioxide is desorbed from said scrubbing solution, the improvement which comprises providing an asymmetrical sterically hindered cycloaliphatic diamine as an amine activator wherein the sterically hindered cycloaliphatic diamine is defined as a compound having a boiling point of at least 80° C. and containing at least one secondary amino group attached to a secondary carbon atom.

Claim 41

The process of claim 33 wherein said scrubbing solution additionally includes an additive selected from the group consisting of antifoaming agents, antioxidants, corrosion inhibitors and mixtures thereof.

Claim 42

The process of claim 33 wherein the scrubbing solution from step (2) which has been desorbed is reused to absorb a feed containing carbon dioxide.

Claim 43

The process of claim 33 wherein said contacting in step (1) (absorption step) takes place at a temperature ranging from about 25° to about 200° C. and at a pressure ranging from about 5 to about 2000 psig for a period ranging from 0.1 to 60 minutes.

Claim 44

The process of claim 33 wherein the scrubbing solution is regenerated at a temperature ranging from 25 to 200° C. and at a pressure ranging from about 16 to about 100 psia.

Claim 45

The process of claim 33 wherein the gaseous feed contains CO 2 and H 2 S.