Method of making a crosslinked fiber membrane from a high molecular weight, monoesterified polyimide polymer

• US 8,328,906 B2
• Filed: 11/28/2011
• Issued: 12/11/2012
• Est. Priority Date: 01/10/2008
• Status: Expired due to Fees

• Current Assignee: Chevron USA Incorporated (Chevron Corp.), Georgia Tech Research Corporation (University System of Georgia)
• Original Assignee: Chevron USA Incorporated (Chevron Corp.), Georgia Tech Research Corporation (University System of Georgia)
• Inventors: Omole, Imona C., Kronos, William J., Miller, Stephen J.
• Primary Examiner(s): Greene, Jason M
• Application Number:
  US13/305,350
• Publication Number:
  US 20120067208A1
• Time in Patent Office: 379 Days
• Field of Search: 95/45, 95/47, 95/51, 95/54, 96/4, 96/7, 96/8, 96/9, 96/10, 96/11, 96/12, 96/13, 96/14, 555/24, 55D/IG.5, 210/640, 210/650, 210/500.27, 210/500.37, 210/506, 525/420, 525/422, 525/423, 525/436, 524/538, 524/599, 264/210.1, 264/203, 264/209.1
• US Class Current: 95/45
• CPC Class Codes: C08G 73/1039 comprising halogen-containing substituents
• CPC Class Codes: C08G 73/1042 Copolyimides derived from at least two different tetracarboxylic compounds or two different diamino compounds
• CPC Class Codes: C08G 73/1067 Wholly aromatic polyimides, i.e. having both tetracarboxylic and diamino moieties aromatically bound
• CPC Class Codes: D01D 5/24 with a hollow structure; Spinnerette packs therefor D01D5/38 takes precedence; producing tubes of plastic material B29D; addition of agents forming hollow filaments D01F1/08
• CPC Class Codes: D01F 6/74 from polycondensates of cyclic compounds, e.g. polyimides, polybenzimidazoles

Abstract

The present disclosure relates to a high molecular weight, monoesterified polyimide polymer. Such high molecular weight, monoesterified polyimide polymers are useful in forming crosslinked polymer membranes for the separation of fluid mixtures. According to its broadest aspect, the method of making a crosslinked membrane comprises the following steps: (a) preparing a polyimide polymer comprising carboxylic acid functional groups from a reaction solution comprising monomers and at least one solvent; (b) treating the polyimide polymer with a diol at esterification conditions in the presence of dehydrating conditions to form a monoesterified polyimide polymer; and (c) subjecting the monoesterified fiber to transesterification conditions to form a crosslinked fiber membrane, wherein the dehydrating conditions at least partially remove water produced during step (b). The crosslinked membranes can be used to separate at least one component from a feed stream including more than one component.

Claims

1. A method of making a crosslinked membrane, comprising:

(a) preparing a polyimide polymer comprising carboxylic acid functional groups from a reaction solution comprising monomers and at least one solvent, with the preparation of the polyimide polymer taking place under dehydrating conditions such that the concentration of water in the reaction solution is maintained at between about 0 weight percent and 0.26 weight percent;

(b) treating the polyimide polymer with a diol at esterification conditions in the presence of dehydrating conditions to form a monoesterified polyimide polymer, with the dehydrating conditions at least partially removing water produced during step (b); and

(c) subjecting the monoesterified polyimide polymer to transesterification conditions to form a crosslinked membrane.

2. The method of claim 1, wherein the crosslinked membrane is a crosslinked hollow fiber membrane and the method further comprises forming monesterified fiber from the monesterified polyimide polymer and subjecting the monesterified fiber to transesterification conditions to form a crosslinked hollow fiber membrane.

3. The method of claim 1, wherein the dehydrating conditions of step (b) are a chemical dehydrating agent.

4. The method of claim 3, wherein the chemical dehydrating agent is an azeotropic chemical dehydrating agent or a carbodiimide.

5. The method of claim 4, wherein the azeotropic chemical dehydrating agent is selected from the group consisting of orthodichlorobenzene (ODCB), benzene, toluene, and mixtures thereof.

6. The method of claim 1, wherein the dehydrating conditions of step (b) are a mechanical dehydrating agent.

7. The method of claim 6, wherein the mechanical dehydrating agent is a Dean-Stark trap.

8. The method of claim 1, wherein the dehydrating conditions of step (b) comprise a chemical dehydrating agent and a mechanical dehydrating agent.

9. The method of claim 1, wherein the dehydrating conditions of step (a) are a chemical dehydrating agent.

10. The method of claim 9, wherein the chemical dehydrating agent is an azeotropic chemical dehydrating agent or a carbodiimide.

11. The method of claim 10, wherein the azeotropic chemical dehydrating agent is selected from the group consisting of orthodichlorobenzene (ODCB), benzene, toluene, and mixtures thereof.

12. The method of claim 1, wherein the dehydrating conditions of step (a) are a mechanical dehydrating agent.

13. The method of claim 12, wherein the mechanical dehydrating agent is a Dean-Stark trap.

14. The method of claim 1, wherein the dehydrating conditions of step (a) comprise a chemical dehydrating agent and a mechanical dehydrating agent.

15. The method of claim 2, wherein the forming step comprises spinning the monoesterified hollow fiber from a spinning dope comprising the monoesterified polyimide polymer, a volatile component, a spinning solvent, a spinning non-solvent, and optionally an inorganic additive.

16. The method of claim 15, wherein the monoesterified polyimide polymer is present in the spinning dope in an amount between about 20 and about 50 weight percent.

17. The method of claim 15, wherein the volatile component is present in the spinning dope in an amount between about 5 and about 25 weight percent.

18. The method of claim 15, wherein the inorganic additive is an antilyotropic salt.

19. The method of claim 15, wherein the volatile component is an organic solvent having a room temperature vapor pressure greater than about 0.05 bar and a normal boiling point between about 30°

C. and about 100°

C.

20. The method of claim 19, wherein the volatile component is selected from the group consisting of tetrahydrofuran (THF), acetone, and mixtures thereof.

21. The method of claim 18, wherein the antilyotropic salt is present in the spinning dope in an amount between about 0 and about 10 weight percent.

22. The method of claim 15, wherein the spinning solvent is an organic solvent selected from the group consisting of N-methyl-2-pyrrolidone (NMP), dimethyl sulfoxide (DMSO), dimethylformamide (DMF), dimethylacetamide (DMAc), and diglyme.

23. The method of claim 15, wherein the spinning non-solvent is selected from the group consisting of an aliphatic alcohol, water, and mixtures thereof.

24. The method of claim 15, wherein the concentrations of the spinning solvent and the spinning non-solvent in the spinning dope are determined by a precipitation method, the precipitation method comprising:

(i) setting the concentrations of the monoesterified polyimide polymer, the volatile component, and the optional inorganic additive;

(ii) choosing initial concentrations of the spinning solvent and the spinning non-solvent;

(iii) combining the monoesterified polyimide polymer, the volatile component, the optional inorganic additive, the spinning solvent, and the spinning non-solvent to provide a spinning dope sample;

(iv) if the polymer precipitates out, increasing the concentration of the spinning solvent between about 0 weight percent and about 5 weight percent to arrive at a final spinning solvent concentration and similarly decreasing the concentration of the spinning non-solvent to arrive at a final spinning non-solvent concentration; and

(v) if the polymer does not precipitate out, altering the initial concentrations of the spinning solvent and/or the spinning non-solvent and repeating steps (iii)-(v) until the spinning dope sample is a homogeneous single phase.

25. The method of claim 15, wherein the monoesterified hollow fiber is spun from the spinning dope by a dry-jet/wet-quench spinning process comprising:

(a) extruding the monoesterified polyimide polymer through orifices of a spinneret to provide a monoesterified hollow fiber;

(b) conveying the monoesterified hollow fiber through an air gap and through a coagulating bath of de-ionized water; and

(c) winding the monoesterified hollow fiber around a take-up drum at a take-up rate between about 10 m/min and about 150 m/min,

wherein the dry-jet/wet-quench spinning process has a draw ratio of less than 150.

26. The method of claim 25, wherein the temperature of the spinning dope is greater than 40°

C.

27. The method of claim 25, wherein the temperature of the coagulating bath is between about 10°

C. and about 70°

C.

28. The method of claim 25, wherein the dry-jet/wet-quench spinning process has an air gap height that is greater than 5 centimeters.

29. The method of claim 25, wherein the dry-jet/wet-quench spinning process has a face velocity of air surrounding the spinneret that is greater than 50 feet per minute.

30. A method of using the crosslinked membrane made according to the method of claim 1, comprising:

(a) providing a feed stream selected from the group consisting of air, a mixture of methane and nitrogen, a mixture of methane and hydrogen, a mixture of methane and hydrogen sulfide, a refinery stream, a mixture of carbon dioxide and methane, and syngas,

the feed stream including a gaseous component selected from the group consisting of nitrogen, oxygen, hydrogen, hydrogen sulfide and carbon dioxide;

(b) maintaining a pressure differential between an upstream side of the membrane and a downstream side of the membrane;

(c) contacting the upstream side of the membrane with the feed stream at a pressure between about 20 psia and about 4000 psia;

(d) isolating a permeate stream on the downstream side of the membrane having a larger mole fraction of the faster permeating component of the feed stream; and

(e) isolating a retentate stream having a smaller mole fraction of the faster permeating component of the feed stream.

31. The method of claim 30, wherein the crosslinked membrane is a crosslinked hollow fiber membrane.