Removal of acid gases from gaseous mixtures containing them

Patent metadata

Field	Value
Publication number	US-12509639-B2
Application number	US-202118254514-A
Country	US
Kind code	B2
Filing date	Nov 23, 2021
Priority date	Nov 25, 2020
Publication date	Dec 30, 2025
Grant date	Dec 30, 2025

Abstract

An acid gas absorbing mixture and a process for the removal of acid gases from gaseous mixtures containing them, such as natural gas, air and flue gases and
an absorbent mixture usable for the removal of acid gases from gaseous mixtures containing them includes at least one diol of general formula R(OH) 2 having a normal boiling point equal to or greater than 100° C.; at least one organic base having a pK b (in water) lower than or equal to 3; and a polar aprotic solvent having a dielectric constant ε at 25° C. greater than or equal to 30, a viscosity μ at 25° C. lower than or equal to 40 cP (centipoise).
The organic base/diol weight ratio is lower than or equal to 0.6, and the aprotic solvent/diol weight ratio is between 0.05 and 0.6.

First claim

The invention claimed is:

1 . An absorbent mixture usable for the removal of acid gases from gaseous mixtures containing them, the absorbent mixture comprising:
A) at least one diol of general formula R(OH) 2 having a normal boiling point equal to or greater than 100° C., wherein R is an alkyl group, linear or branched, possibly substituted, having a number of carbon atoms comprised between 2 and 8; B) at least one organic base having a pK b (in water) lower than or equal to 3; C) a polar aprotic solvent having a dielectric constant F at 25° C. greater than or equal to 30, a viscosity p at 25° C. lower than or equal to 40 cP (centipoise), and a normal boiling point equal to or greater than 140° C.,
and wherein
the organic base/diol weight ratio is lower than or equal to 0.6,
the aprotic solvent/diol weight ratio is comprised between 0.05 and 0.6,

wherein the polar aprotic solvent is selected from dimethyl sulfoxide (DMSO), sulfolane (SO) and nitrobenzene (NB), preferably sulfolane.

2 . The absorbent mixture according to claim 1 , wherein the organic base/diol weight ratio is comprised between 0.45 and 0.55, or is comprised between 0.45 and 0.5.

3 . The absorbent mixture according to claim 1 , wherein the aprotic solvent/diol weight ratio is comprised between 0.08 and 0.5, or between 0.08 and 0.2.

4 . The absorbent mixture according to claim 1 , wherein the ratio between the moles of OH groups of the diol A) and the moles of base B) in the reaction mixture is comprised between 10/1 and 6/1, or is comprised between 8/1 and 6/1.

5 . The absorbent mixture according to claim 1 , wherein the diol R(OH) 2 has an alkyl group R comprised between 2 and 3 carbon atoms, or the diol R(OH) 2 is selected from the group consisting of ethylene glycol, propylenic glycol, and 1,3-propandiol.

6 . The absorbent mixture according to claim 1 , wherein said organic base B) has a pK b lower than or equal to 2, or comprised between 0.3 and 2, or comprised between 0.5 and 2.

7 . The absorbent mixture according to claim 6 , wherein said organic base B) is a nitrogenous organic compound having a low volatility, comprising from 5 to 25, C atoms and from 1 to 10, N atoms, or the organic base B) is selected from the group consisting of 1,8-diazabicyclo (5.4.0) undec-7-ene (DBU) [pK b 1.1], 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) [pK b 0.5], 1,1,3,3-tetramethylguanidine (TMG) [pK b 0.4], derivates of biguanide (1-(diaminomethylidene)guanidine such as N″-[(dimethylamino)(methylimino)methyl]-N,N,N′,N′-tetramethyl-guanidine, 1,8-bis-(tetramethyl-guanidino) naphthalene, compounds of the phosphazene type such as N″,N″″′,N″″″″-phosphinimylidinetris[N,N,N′,N′-tetramethylguanidine], 1,8-bis(tetramethylamino) naphthalene or mixture thereof.

8 . The absorbent mixture according to claim 1 , comprising:
A) 1,2-propandiol or 1,3-propandiol in weight percentage comprised between 55% and 65%; B) diazabicycloundecene (DBU) in weight percentage comprised between 25% and 35%; C) sulfolane in weight percentage comprised between 5% and 15%.

9 . A process for the removal of acid gases from a gaseous mixture containing them, said gaseous mixture consisting of natural gas or of an exhaust smoke from a combustion process, the process including the following steps in sequence:
(a) contacting said gaseous mixture, at a temperature comprised between 0° C. and 70° C. and at a pressure comprised between 50 kPa and 15 MPa, with a solvent system comprising an absorbent mixture as defined in claim 1 , to obtain a purified gaseous mixture and a liquid solution comprising at least a part of said acid gases, (b) separating the purified gaseous mixture from said liquid solution obtained in step (a), c) regenerating the solvent system usable in step (a) and forming a separate gaseous mixture comprising said acid gases, by heating said liquid solution separated in step (b), and d) optionally, recycling the regenerated solvent in step (c) to said step (a).

Assignees

• Eni Spa

Inventors

• De Angelis Alberto Renato
• Fiori Gianluca
• Castaldo Filomena

Classifications

• C10L3/103

  Sulfur containing contaminants · CPC title

• B01D2258/0283

  Flue gases · CPC title

• B01D2257/504

  Carbon dioxide · CPC title

• B01D2257/304

  Hydrogen sulfide · CPC title

• B01D2252/504

  Mixtures of two or more absorbents · CPC title