Composite nanoparticle stabilized core carbon molecular sieve hollow fiber membranes having improved permeance

Patent metadata

Field	Value
Publication number	US-10500548-B2
Application number	US-201515512100-A
Country	US
Kind code	B2
Filing date	Aug 14, 2015
Priority date	Sep 22, 2014
Publication date	Dec 10, 2019
Grant date	Dec 10, 2019

Abstract

Disclosed herein are asymmetric multilayer carbon molecular sieve (“CMS”) hollow fiber membranes and processes for preparing the membranes. The processes include simultaneously extruding a core dope containing a polymer and suitable nanoparticles, a sheath dope, and a bore fluid, followed by pyrolysis of the extruded fiber.

First claim

The invention claimed is:

1. A process for preparing an asymmetric multilayer carbon molecular sieve (CMS) hollow fiber membrane comprising
a. co-extruding a core dope and a sheath dope through a spinneret to produce at least one multilayer CMS membrane precursor fiber,
wherein the core dope comprises a first polymer, a first solvent, and a plurality of nanoparticles, and
wherein the sheath dope comprises a second polymer and a second solvent; and

b. pyrolyzing the at least one multilayer CMS membrane precursor fiber to form an asymmetric multilayer CMS hollow fiber membrane.

2. The process of claim 1 , wherein the first and second polymers are the same polymer.

3. The process of claim 1 , wherein the first and second polymers are different polymers.

4. The process of claim 3 , wherein the first polymer has a glass transition temperature and the second polymer has a glass transition temperature that is equal to or greater than the glass transition temperature of the first polymer.

5. The process of claim 3 , wherein the first polymer has a glass transition temperature and the second polymer has a glass transition temperature that is equal to or lower than the glass transition temperature of the first polymer.

6. The process of claim 1 wherein the plurality of nanoparticles in the core dope are hydrophobic.

7. The process of claim 1 wherein the plurality of nanoparticles in the core dope are polyhedral oligomeric silsesquioxane (“POSS”) silica nanoparticles.

8. The process of claim 1 , wherein the at least one CMS membrane precursor fiber comprises a core layer comprising the extruded core dope and a sheath layer comprising the extruded sheath dope, the core layer having a substantially annular cross-section and the sheath layer having a substantially annular cross-section adjacent to and radially outward from the core layer, and wherein the core layer comprises 25-40 wt % nanoparticles based on polymer weight.

9. The process of claim 1 , wherein the at least one CMS membrane precursor fiber comprises a core layer comprising the extruded core dope and a sheath layer comprising the extruded sheath dope, the core layer having a substantially annular cross-section and the sheath layer having a substantially annular cross-section adjacent to and radially outward from the core layer, and wherein the core layer comprises 10-25 wt % nanoparticles based on polymer weight.

10. The process of claim 1 , further comprising prior to pyrolyzing the CMS hollow fiber membrane precursor, contacting the CMS hollow fiber membrane precursor with one or more solvent exchange materials comprising a modifying agent in an amount effective to improve the gas permeance of the asymmetric multilayer CMS hollow fiber membrane.

11. The process of claim 10 , wherein the modifying agent is a silane.

12. A process for preparing a multilayer hollow fiber membrane comprising:
a. co-extruding a core dope and a sheath dope through a spinneret to produce at least one multilayer hollow fiber membrane precursor,
wherein the core dope comprises a first polymer, a first solvent, and a plurality of nanoparticles, and
wherein the sheath dope comprises a second polymer and a second solvent, wherein the second polymer is a thermally rearrangable polymer; and

b. heating the multilayer hollow fiber membrane precursor at a temperature of between about 270° C. and about 450° C. for a period of about 1 to 4 hours to form an asymmetric composite thermally rearranged hollow fiber membrane.

13. The process of claim 12 , wherein the thermally rearrangable polymer is selected from the group consisting of polybenzoxazoles, polybenzothiazoles, polybenzimidazoles, and combinations.

14. An asymmetric multilayer CMS hollow fiber membrane comprising
a. a core layer comprising a pyrolyzed first polymer and a plurality of nanoparticles, wherein the core layer has a substantially annular cross-section; and
b. a sheath layer comprising a pyrolyzed second polymer, wherein the sheath layer has a substantially annular cross-section and is adjacent to and radially outward from the core layer.

15. The asymmetric multilayer CMS hollow fiber membrane of claim 14 ,
wherein the asymmetric multilayer CMS hollow fiber membrane comprises a gas permeance at least 300% greater than a gas permeance of an otherwise equivalent asymmetric multilayer CMS hollow fiber membrane that does not include nanoparticles in the core layer; or
wherein the asymmetric multilayer CMS hollow fiber membrane comprises a selectivity that is at least 85% of the selectivity of an otherwise equivalent asymmetric multilayer CMS hollow fiber membrane that that does not include nanoparticles in a core layer.

16. The asymmetric multilayer CMS hollow fiber membrane of claim 14 ,
wherein the asymmetric multilayer CMS hollow fiber membrane comprises a CO 2 permeance of at least 50 GPU and a CO 2 /CH 4 selectivity of at least 60 when subjected to a mixed feed containing 50 mol % CO 2 and 50 mol % CH 4 at 150 psi and 35° C.; or
wherein the asymmetric multilayer CMS hollow fiber membrane comprises a O 2 permeance of at least 80 GPU and a O 2 /N 2 selectivity of at least 9 when subjected to a single gas feed at 50 psi and 70° C.; or
wherein the asymmetric multilayer CMS hollow fiber membrane comprises a C 2 H 4 permeance of at least 5 GPU and a C 2 H 4 /C 2 H 6 selectivity of at least 4 when subjected to a single gas feed at 100 psi and 35° C.; or
wherein the asymmetric multilayer CMS hollow fiber membrane comprises a C 3 H 8 permeance of at least 5 GPU and a C 3 H 6 /C 3 H 8 selectivity of at least 20 when subjected to a mixed feed containing 50 mol % C 3 H 6 and 50 mol % C 3 H 8 at 100 psi and 35° C.

17. A process for separating a mixture of at least two gases comprising contacting the mixture of gases with the asymmetric multilayer CMS hollow fiber membrane of claim 14 to separate the mixture into a permeate stream that is enriched in a first gas and a retentate stream that is enriched in a second gas.

18. The process of claim 17 , wherein the mixture of at least two gases comprises CO 2 and CH 4 ; H 2 S and CH 4 ; CO 2 , H 2 S, and CH 4 ; CO 2 and N 2 ; O 2 and N 2 ; N 2 and CH 4 ; He and CH 4 ; H 2 and CH 4 ; H 2 and C 2 H 4 ; ethylene and ethane; propylene and propane; or ethane/propane and ethylene/propylene.

19. The process of claim 17 , wherein the mixture of at least two gases comprises acid gases and natural gases.

20. The process of claim 17 , wherein the mixture of at least two gases comprises CO 2 and at least one hydrocarbon, and wherein the permeate stream is enriched in CO 2 .

Assignees

• Georgia Tech Res Inst

Inventors

• Koros William John
• Zhang Kuang

Classifications

• B01D2325/32

  Melting point or glass-transition temperatures · CPC title

• B01D2323/18

  Pore-control agents or pore formers · CPC title

• B01D71/025

  Aluminium oxide · CPC title

• B01D69/148

  Organic/inorganic mixed matrix membranes · CPC title

• B01D69/088

  Co-extrusion; Co-spinning · CPC title