IP Library › Granted Patent US 11,642,629
Granted Patent B2
US 11,642,629 · App. 16/825,523 · Granted May 9, 2023

Multi-layer composite gas separation membranes, methods for preparation, and use

Inventors: Garba Oloriegbe Yahaya (Dhahran, SA); Seung-Hak Choi (Dhahran, SA); Ahmad Bahamdan (Dhahran, SA)
B01D69/125B01D53/228B01D67/0006B01D67/0095B01D69/02B01D69/105B01D71/64C10L3/101C10L3/104C10L3/105B01D2323/30B01D2323/42B01D2325/04C10L2290/548
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Quick Facts
Patent No.
US 11,642,629
App. No.
16/825,523
Granted
May 9, 2023
Kind
B2
Abstract

Methods and systems for producing and using multi-layer composite co-polyimide membranes, one method for producing including preparing a microporous or mesoporous membrane support material for coating; applying a sealing layer to the membrane support material to prevent intrusion into the membrane support material of co-polyimide polymer; applying a first permselective co-polyimide layer atop and in contact with the sealing layer; and applying a second permselective co-polyimide layer atop and in contact with the first permselective co-polyimide layer.

Claims (34)

1. A method for producing a multi-layer composite co-polyimide membrane, the method comprising the steps of:

preparing a microporous or mesoporous membrane support material for coating;

applying a sealing layer to the membrane support material to prevent intrusion into the membrane support material of a co-polyimide polymer;

applying a first permselective co-polyimide layer comprising the co-polyimide polymer, the co-polyimide polymer comprising block (6FDA-CARDO)/(6FDA-durene) atop and in contact with the sealing layer; and

applying a second permselective co-polyimide layer comprising block (6FDA-CARDO)/(6FDA-durene) atop and in contact with the first permselective co-polyimide layer.

2. The method according to claim 1 , where the first permselective co-polyimide layer and second permselective co-polyimide layer further comprise random co-polymers.

3. The method according to claim 2 , where the first permselective co-polyimide layer and second permselective co-polyimide layer comprise the same random co-polymers.

4. The method according to claim 1 , where the first permselective co-polyimide layer and second permselective co-polyimide layer result in a thickness between about 1-3 μm.

5. The method according to claim 1 , where the sealing layer comprises a solvent material being the same as a solvent material into which a first co-polyimide of the first permselective co-polyimide layer and into which a second co-polyimide of the second permselective co-polyimide layer are dissolved for the steps of applying the first permselective co-polyimide layer and second permselective co-polyimide layer.

6. The method according to claim 1 , where the sealing layer further comprises a gutter layer.

7. The method according to claim 6 , where the gutter layer comprises poly [1-(trimethylsilyl)-1-propyne] (PTMSP).

8. The method according to claim 1 , where the microporous or mesoporous membrane support material for coating includes a support material selected from the group consisting of: flat sheet support material; hollow fiber support material; and combinations thereof.

9. The method according to claim 1 , further comprising a step of crosslinking the first permselective co-polyimide layer and the second permselective co-polyimide layer.

10. The method according to claim 1 , where the sealing layer comprises a component selected from the group consisting of: Chloroform (CHCl 3 ); N,N-dimethylformamide (DMF); dichloromethane (DCM); N,N-dimethyl acetamide (DMAc); Acetone; Tetrahydrofuran (THF); N-Methyl-2-pyrrolidone (NMP); tetra chloromethane (CCl 4 )); and combinations of the same.

11. The method according to claim 1 , where a step of drying is carried out after each of the steps of applying the sealing layer, applying the first permselective co-polyimide layer, and applying the second permselective co-polyimide layer.

12. The method according to claim 1 , further comprising a step of formulating a first co-polyimide for the first permselective co-polyimide layer and a step of formulating a second co-polyimide for the second permselective co-polyimide layer, where the steps of formulating comprise combining more than one monomer in a mixture of monomers, where the more than one monomer is selected from the group consisting of: 2,2′-bis-(3,4-dicarboxyphenyl) hexafluoropropane dianhydride (6FDA); 1,3-phenylenediamine (mPDA); durene diamine; 3,4,9,10-perylentetracarbonsauredianhydrid (PTCDA); pyromellitic dianhydride (PMDA); 1,4-bis(4-aminophenoxy)triptycene (BAPT); 4,5,6,7-Tetrabromo-2-azabenzimidazole (TBB); 4,4′-(9-Fluorenylidene)dianiline (FDA); and 4,4′-Oxydiphthalic anhydride (ODA).

13. The method according to claim 1 , where the first permselective co-polyimide layer or second permselective co-polyimide layer further comprises a polymer unit selected from the group consisting of: (6FDA-mPDA)/(6FDA-durene); (6FDA-PTCDA-FDA); (6FDA-TBB-FDA); (6FDA-B APT-FDA); (PTCDA-FDA)/(PMDA-mPDA); (PMDA-FDA)/(PTCDA-mPDA); (ODA-FDA)/(PTCDA-mPDA); (6FDA-BAPT)/(6FDA-FDA); (PTCDA-mPDA)/(6FDA-FDA); (PTCDA-FDA)/(ODA-mPDA); (PTCDA-FDA)/(6FDA-FDA); (6FDA-TBB)/(6FDA-FDA); (6FDA-TBB)/(6FDA-durene); (6FDA-mPDA)/(6FDA-B APT); (PTCDA-mPDA)/(6FDA-FDA); (6FDA-mPDA-BAPT); and (6FDA-FDA-mPDA).

14. The method according to claim 1 , further comprising a step of formulating a first co-polyimide for the first permselective co-polyimide layer and a step of formulating a second co-polyimide for the second permselective co-polyimide layer, where the steps of formulating comprise combining at least three distinct moieties polymerized together, the moieties including a 2,2′-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety; a 9,9-bis(4-aminophenyl) fluorene (CARDO) based moiety; and 2,3,5,6-tetramethyl-1,4-phenylenediamine (durene diamine) based moiety.

15. The method according to claim 1 , further comprising a step of formulating a first co-polyimide for the first permselective co-polyimide layer and a step of formulating a second co-polyimide for the second permselective co-polyimide layer, where the steps of formulating comprise combining at least three distinct moieties polymerized together, the three distinct moieties including a first moiety, a second moiety, and a third moiety;

wherein the first moiety comprises a 2,2′-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety;

the second moiety comprises a 4,4′-(hexafluoroisopropylidene)dianiline (6FpDA) based moiety; and

the third moiety comprises a component selected from the group consisting of: a 9,9-bis(4-aminophenyl) fluorene (CARDO) based moiety; a 2,3,5,6-tetramethyl-1,4-phenylenediamine (durene diamine) based moiety; a 2,2′-bis(trifluoromethyl)benzidine (ABL-21) based moiety; a 3,3′-dihydroxybenzidine based moiety; and a 3,3′-(hexafluoroisopropylidene)dianiline based moiety.

16. The method according to claim 1 , further comprising a step of formulating a first co-polyimide for the first permselective co-polyimide layer and a step of formulating a second co-polyimide for the second permselective co-polyimide layer, where the steps of formulating comprise combining at least three distinct moieties polymerized together, the three distinct moieties including a first moiety, a second moiety, and a third moiety;

wherein the first moiety comprises a 2,2′-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety;

the second moiety comprises a 2,4,6-trimethyl-m-phenylenediamine (DAM) based moiety; and

the third moiety comprises a component selected from the group consisting of: a 4,4′-(hexafluoroisopropylidene)dianiline (6FpDA) based moiety; a 9,9-bis(4-aminophenyl) fluorene (CARDO) based moiety; a 2,3,5,6-tetramethyl-1,4-phenylenediamine (durene diamine) based moiety; a 2,2′-bis(trifluoromethyl)benzidine (ABL-21) based moiety; a 3,3′-dihydroxybenzidine based moiety; and a 3,3′-(hexafluoroisopropylidene)dianiline based moiety.

17. The method according to claim 1 , where the first permselective layer or second permselective layer comprises a 2,2′-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety and a 2,2′-bis(trifluoromethyl)benzidine (ABL-21) based moiety.

18. The method according to claim 1 , further comprising the step of formulating a first co-polyimide for the first permselective co-polyimide layer and formulating a second co-polyimide for the second permselective co-polyimide layer, where the steps of formulating comprise combining at least three distinct moieties polymerized together, the three distinct moieties including a first moiety, a second moiety, and a third moiety;

wherein the first moiety comprises a dianhydride selected from the group consisting of: a 2,2′-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA) based moiety; a benzophenone-3,3′, 4,4′-tetracarboxylic dianhydride (BTDA) based moiety; and a pyromellitic dianhydride (PMDA) based moiety;

wherein the second moiety comprises a 2,4,6-trimethyl-m-phenylenediamine (DAM) based moiety; and

wherein the third moiety comprises a component selected from the group consisting of: a 4,4′-(hexafluoroisopropylidene)dianiline (6FpDA) based moiety; a 9,9-bis(4-aminophenyl) fluorene (CARDO) based moiety; a 2,3,5,6-tetramethyl-1,4-phenylenediamine (durene diamine) based moiety; a 2,2′-bis(trifluoromethyl)benzidine (ABL-21) based moiety; a 3,3′-dihydroxybenzidine based moiety; and a 3,3′-(hexafluoroisopropylidene)dianiline based moiety.

19. A method of gas separation, the method comprising the step of:

applying the multi-layer composite co-polyimide membrane of claim 1 to separate at least 2 components of a mixed gas stream.

20. The method according to claim 19 , where feed pressure of the mixed gas stream to a feed side of the membrane is up to about 900 psig and H 2 S content of the mixed gas stream is up to about 22 volume percent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2020
From: YAHAYA, GARBA OLORIEGBE; CHOI, SEUNG-HAK; BAHAMDAN, AHMAD
To: SAUDI ARABIAN OIL COMPANY
Reel/Frame 052179/0806 →
Continuity (1)
Related Publication 20210291120A1 · Sep 23, 2021
Cited By (1)
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