IP Library Granted Patent US 8,426,070
Granted Patent B2
US 8,426,070 · App. 12/747,831 · Granted Apr 23, 2013

Method for removing diluent from an extrudate of a polymer solution

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Quick Facts
Patent No.
US 8,426,070
App. No.
12/747,831
Granted
Apr 23, 2013
Kind
B2
Abstract

The invention relates to a method for removing diluent from a polymer extrudate, especially in connection with a process for producing a microporous membrane. The method involves contacting the extrudate with a second solvent in a first stage; contacting the extrudate from the first stage with a third solvent in a second stage; conducting a first stream away from the first stage and/or conducting a second stream away from the second stage; and cooling at least a portion of the first and/or second stream and separating therefrom at least one of a first phase rich in the second solvent or a second phase rich in the third solvent.

Claims (54)

1. A process for removing a first solvent from a porous polymeric extrudate comprising:

(A) contacting the extrudate with a second solvent in a first stage;

(B) contacting the extrudate from step (A) with a third solvent in a second stage;

(C) conducting a first stream away from the first stage, the first stream comprising at least a portion of the second solvent in the first stage and/or conducting a second stream away from the second stage, the second stream

comprising at least a portion of the third solvent in the second stage, and separating the first solvent from the first stream, the second stream, or both; and

(E) cooling at least a portion of the first and/or second stream and separating therefrom at least one of a first phase rich in the second solvent or a second phase rich in the third solvent.

2. The process according to claim 1 wherein at least a portion of each of the first and second streams from step (C) are combined in a step (D) prior to step (E) and wherein at least a portion of the first solvent is separated from the first stream and/or the combined streams prior to step (E).

3. The process according to claim 1 wherein the first solvent comprises liquid paraffin.

4. The process according to claim 1 , wherein the second solvent comprises at least one chlorinated hydrocarbon (CHC), and wherein the third solvent comprises at least one hydrofluoroether (HFE).

5. The process according to claim 4 the hydrofluoroether is at least one of C 4 F 9 OCH 3 , C 4 F 9 OC 2 H 5 and C 6 F 13 OCH 3 .

6. The process according to claim 4 wherein the chlorinated hydrocarbon is at least one of dichloromethane, trichloromethane, tetrachloromethane, 1,1-dichloroethane, 1,2-dichloroethane and trichloroethane.

7. The process according to claim 4 , wherein the first phase is a CHC-rich phase and wherein the second phase is an HFE-rich phase, and further comprising a step (F) of at least one of

(a) conducting at least a portion of the CHC-rich phase from step (E) to step (A);

(b) conducting at least a portion of the HFE-rich phase from step (E) to step (B);

(c) (i) separating a first and second product, from the CHC-rich phase of step (E) wherein the first product comprises relatively pure chlorinated hydrocarbon and the second product comprises at least a portion of the remainder of the CHC-rich phase of step (E) following separation of the first product, and carrying out the steps of (c) (ii) and/or (c)(iii)

(ii) conducting at least a portion of the first product to step (A),

(iii) conducting at least a portion of the second product to at least step (A) and/or step (E);

or

(d) (i) separating a third and fourth product from the HFE-rich phase of step (E) wherein the third product comprises relatively pure hydrofluoroether and the fourth product comprises at least a portion of the remainder of the HFE-rich phase of step (E) following separation of the third product, and then carrying out the steps of (d)(ii) and/or (d)(iii)

(ii) conducting at least a portion of the third product to step (B),

(iii) conducting at least a portion of the fourth product to steps (A) and/or (E).

8. The process according to claim 1 , wherein the process is operated continuously.

9. The process according to claim 7 wherein the CHC-rich phase is an azeotrope of chlorinated hydrocarbon and hydrofluoroether.

10. The process according to claim 7 wherein the second and fourth products are an azeotrope of chlorinated hydrocarbon and hydrofluoroether and wherein the second and fourth products are recycled to extinction in step (E).

11. A process for producing a microporous polymeric film, the process comprising

(2) combining polymer resin(s) and one or more process solvents to form a polymeric solution;

(3) extruding the polymeric solution to produce a polymeric extrudate;

(5) removing at least a portion of the process solvent from the extrudate by the steps of

(A) contacting the extrudate with a second solvent comprising at least one chlorinated hydrocarbon (CHC) in a washing stage; and then

(B) contacting the washed extrudate from step (A) with a third solvent comprising at least one hydrofluoroether (HFE) in a rinsing stage,

(C) conducting a first stream away from the washing stage, the first stream comprising at least a portion of the chlorinated hydrocarbon in the washing stage and/or conducting a second stream away from the rinsing stage, the second stream comprising at least a portion of the hydrofluoroether in the rinsing stage; and

(E) cooling at least a portion of the first and/or at least a portion second stream, and separating therefrom a first phase rich in chlorinated hydrocarbon, a second phase rich in hydrofluoroether, or both the first phase and the second phase.

12. The process according to claim 11 wherein at least a portion of each of the first and second streams from step 5(C) are combined in a step 5(D) prior to step 5(E) and wherein at least a portion of the first solvent is separated from the first stream and/or the combined streams prior to step 5(E); and wherein the process further comprises a step (1) of combining polymer resins.

13. The process according to claim 11 wherein the first solvent comprises liquid paraffin.

14. The process according to claim 11 , the hydrofluoroether is at least one of C 4 F 9 OCH 3 , C 4 F 9 OC 2 H 5 and C 6 F 13 OCH 3 .

15. The process according to claim 11 , wherein the chlorinated hydrocarbon is at least one of dichloromethane, trichloromethane, tetrachloromethane, 1,1-dichloroethane, 1,2-dichloroethane and trichloroethane.

16. The process according to claim 13 , wherein the first phase is a CHC-rich phase and wherein the second phase is an HFE-rich phase, and further comprising step (F) of

(a) conducting at least a portion of the CHC-rich phase from step (E) to step (A);

(b) conducting at least a portion of the HFE-rich phase from step (E) to step (B);

(c) (i) separating a first and second product, from the CHC-rich phase of step (E) wherein the first product comprises relatively pure chlorinated hydrocarbon and the second product comprises at least a portion of the remainder of the CHC-rich phase of step (E) following separation of the first product, and then carrying out the steps of (c) (ii) and/or (c)(iii)

(ii) conducting at least a portion of the first product to step (A),

(iii) conducting at least a portion of the second product to at least step (A) and/or step (E);

or

(d) (i) separating a third and fourth product from the HFE-rich phase of step (E) wherein the third product comprises relatively pure hydrofluoroether

and the fourth product comprises at least a portion of the remainder of the HFE-rich phase of step (E) following separation of the third product, and then carrying out the steps of (d)(ii) and/or (d)(iii)

(ii) conducting at least a portion of the third product to step (B),

(iii) conducting at least a portion of the fourth product to steps (A) and/or (E).

17. The process according to claim 11 , wherein the process is operated continuously.

18. The process according to claim 16 wherein the CHC-rich phase is an azeotrope of chlorinated hydrocarbon and hydrofluoroether.

19. The process according to claim 16 wherein the second and fourth products are an azeotrope of chlorinated hydrocarbon and hydrofluoroether and wherein the second and fourth products are recycled to extinction in step (E).

20. The process according to claim 11 , further comprising step (4) of cooling and/or stretching the extrudate of step (3).

21. A microporous membrane made by the process of claim 11 .

22. A battery comprising an anode, a cathode, an electrolyte, and a battery separator located between the anode and the cathode, wherein the battery separator comprises the microporous membrane of claim 21 .

23. A source or sink of electric charge comprising the battery of claim 22 .

Assignments (6)
MERGER Recorded Sep 15, 2017
From: TORAY BATTERY SEPARATOR FILM CO., LTD.
To: TORAY INDUSTRIES, INC.
Reel/Frame 043968/0447 →
PLEASE REPLACE CHANGE OF NAME AT REEL 029108/0702, AS THE NAME OF THE CONVEYING PARTY WAS ERRONEOUSLY INDICATED Recorded Jan 31, 2013
From: TORAY TONEN SPECIALTY SEPARATOR GODO KAISHA
To: TORAY BATTERY SEPARATOR FILM GODO KAISHA
Reel/Frame 029956/0850 →
CHANGE OF NAME Recorded Oct 10, 2012
From: TORAY BATTERY SEPARATOR FILM GODO KAISHA
To: TORAY BATTERY SEPARATOR FILM CO., LTD.
Reel/Frame 029104/0888 →
CHANGE OF NAME Recorded Oct 10, 2012
From: TONEN SPECIALTY SEPARATOR GODO KAISHA
To: TORAY BATTERY SEPARATOR FILM GODO KAISHA
Reel/Frame 029108/0702 →
NUNC PRO TUNC ASSIGNMENT Recorded Mar 28, 2011
From: TONEN CHEMICAL CORPORATION
To: TORAY TONEN SPECIALTY SEPARATOR GODO KAISHA
Reel/Frame 026029/0070 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2010
From: KIMISHIMA, KOTARO; SUZUKI, SADAKATSU
To: TONEN CHEMICAL CORPORATION
Reel/Frame 024525/0628 →