IP Library Granted Patent US 6,962,966
Granted Patent B2
US 6,962,966 · App. 09/727,637 · Granted Nov 8, 2005

Monohydric polyfluorooxetane oligomers, polymers, and copolymers and coatings containing the same

Assignee: OMNOVA Solutions Inc.
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Quick Facts
Patent No.
US 6,962,966
App. No.
09/727,637
Granted
Nov 8, 2005
Kind
B2
Abstract

Monofunctional polyfluorooxetane oligomers, polymers, and co-polymers are prepared by the cationic polymerization of fluorooxetane monomers with a monoalcohol. In addition to serving as an initiator, the monoalcohol can also serve as a solvent for the fluorooxetane or other monomers to produce oligomers, polymers, or copolymers having low cyclic content. Suitable comonomers generally include various cyclic ethers. The polyfluorooxetane oligomer, polymer, or copolymer having a single hydroxyl end group can be functionalized with a variety of compounds so as to yield a functional end group such as an acrylate, a methacrylate, an allylic, an amine, etc., with the functionalized oligomer or polymer being suitable for use in radiation curable or thermal curable coating compositions. These functionalized polymers can be copolymerized and cured to provide improvements in wetting and surface properties.

Claims (49)

1. A monohydric polyfluorooxetane oligomer composition, comprising:

a unit, derived from a fluorooxetane monomer, having the formula

 or combinations thereof, where R 1 is derived from a co-initiator solvent monoalcohol, wherein said composition is derived from a solution having less than about 10% by weight of a non-initiator solvent based upon the total weight of said non-initiator solvent and said monoalcohol,

where Dp is from about 2 to about 20, where each n is the same or different and independently is an integer from 1 to about 6, R is hydrogen or an alkyl of 1 to 6 carbon atoms, and each Rf is the same or different and independently on each repeat unit is a linear or branched fluorinated alkyl of 1 to 20 carbon atoms, a minimum of 75 percent of the non-carbon atoms of the alkyl being fluorine atoms and optionally the remaining non-carbon atoms being H, I, Cl, or Br, and

said monohydric polyfluorooxetane oligomer optionally including at least a comonomer unit derived from a monomer containing at least an epoxy (oxirane) functionality, a monomer having a 4-membered cyclic ether group (oxetane); a monomer having a 5-membered cyclic ether group, 1,4-dioxane, 1,3-dioxane, 1,3-dioxalane, trioxane, or caprolactone; or combinations thereof, in an amount of from about 0.1% to about 10% by weight based upon the total weight of said comonomer and said fluorooxetane monomer, and

said composition having less than about 10% by weight of a cyclic oligomer therein based upon the total weight of said oligomer, and any polymer, or copolymer produced.

2. A monohydric polyfluorooxetane oligomer composition according to claim 1 , wherein said R 1 is derived from said co-initiator solvent monoalcohol comprising an organic alcohol, a polymeric alcohol, a tetrafluoroethylene based telomer fluoroalcohol, or combinations thereof, and wherein the amount of any cyclic oligomer is less than about 8% by weight.

3. A monohydric polyfluorooxetane oligomer composition according to claim 2 , wherein said organic alcohol has from 1 to 40 carbon atoms, wherein said polymeric alcohol contains repeat units derived from an alkylene oxide having from 2 to 6 carbon atoms and the number of repeat groups is from about 3 to about 30, and wherein said tetrafluoroethylene based telomer is CF 3 CF 2 (CF 2 CF 2 ) x CH 2 CH 2 OH where x is from 1 to about 19,

wherein said Dp is from about 2 to about 10, and

wherein each Rf is the same or different and independently is a linear or branched fluorinated alkyl having from 1 to about 15 carbon atoms, said composition having less than about 5% by weight of cyclic oligomer.

4. A monohydric polyfluorooxetane oligomer composition according to claim 3 , wherein said R 1 is derived from benzyl alcohol, trifluoroethanol, allyl alcohol, heptafluorobutanol, pentafluoropropanol, pentafluorobutanol, nonafluorohexanol, various perfluoroalkylethanols, or combinations thereof, and said composition having less than about 3% by weight of cyclic oligomer.

5. A monohydric polyfluorooxetane oligomer composition according to claim 4 , wherein said unit derived from said fluorooxetane monomer is said

wherein n is 1 to about 3, wherein R is methyl or ethyl, and wherein Rf contains from 1 to about 8 carbon atoms, wherein Rf contains a minimum of 85% of the non-carbon atoms of the alkyl being fluorine atoms, wherein said Dp is from about 2 to about 4, and said composition having less than about 1 % by weight of cyclic oligomer.

6. A monohydric polyfluorooxetane copolymer composition according to claim 1 , including at least one of said comonomers.

7. A monohydric polyfluorooxetane copolymer composition according to claim 3 , including said comonomer and wherein said comonomer is tetrahydrofuran.

8. A monohydric polyfluorooxetane copolymer composition according to claim 5 , including said comonomer and wherein said comonomer is tetrahydrofuran.

9. A composition according to claim 1 , wherein said amount of said non-intiator solvent is less than about 5% by weight based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol.

10. A composition according to claim 3 , wherein said amount of said non-intiator solvent is less than about 5% by weight based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol.

11. A composition according to claim 5 , wherein said amount of said non-intiator solvent is less than about 3% by weight based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol.

12. A composition according to claim 6 , wherein said amount of said non-intiator solvent is less than about 5% by weight based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol.

13. A composition according to claim 7 , wherein said amount of said non-intiator solvent is less than about 5% by weight based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol.

14. A composition according to claim 8 , wherein said amount of said non-intiator solvent is less than about 3% by weight based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol.

15. A monohydric polyfluorooxetane oligomer or polymer composition, comprising:

a unit, derived from a fluorooxetane monomer, having the formula

 or combinations thereof, where R 1 is derived from a co-initiator solvent monoalcohol, wherein said composition is derived from a solution having less than about 10% by weight of a non-initiator solvent based upon the total weight of said non-initiator solvent and said co--initiator solvent monoalcohol,

where Dp is from 2 to about 150, where each n is the same or different and independently is an integer from 1 to about 6, R is hydrogen or an alkyl of 1 to 6 carbon atoms, and each Rf is the same or different and independently on each repeat unit is a linear or branched fluorinated alkyl of 1 to 20 carbon atoms, a minimum of 75 percent of the non-carbon atoms of the alkyl being fluorine atoms and optionally the remaining non-carbon atoms being H, I, Cl, or Br; and

said oligomer or polymer optionally including at least one comonomer unit derived from a monomer containing at least an epoxy (oxirane) functionality, a monomer having a 4-membered cyclic ether group (oxetane); a monomer having a 5-membered cyclic ether group, 1,4-droxane, 1,3-dioxane, 1,3-dioxalane, trioxane, or caprolactone; or combinations thereof, in an amount of from about 0.1% to about 10% by weight based upon the total weight of said comonomer and said fluorooxetane monomer.

16. A monohydric polyfluorooxetane composition according to claim 15 , wherein R 1 is derived from siad co-initiator solvent monoalcohol comprising an organic alcohol, a polymeric alcohol, a tetrafluoroethylene based telomer fluoroalcohol, or combinations thereof, and wherein said Dp is from 2 to about 50.

17. A monohydric polyfluorooxetane composition according to claim 16 , wherein said organic alcohol has from 1 to 40 carbon atoms, wherein said polymeric alcohol contains repeat units derived from an alkylene oxide having from 2 to 6 carbon atoms wherein the number of said repeat groups is from about 3 to about 30, and wherein said tetrafluoroethylene based telomer is CF 3 CF 2 (CF 2 CF 2 ) x CH 2 CH 2 OH where x is from 1 to about 19,

wherein said Dp is from about 2 to about 20, and

wherein each Rf is the same or different and independently is a linear or branched fluoronated alkyl having from 1 to about 15 carbon atoms.

18. A monohydric polyfluorooxetane composition according to claim 17 , wherein said R 1 is derived from benzyl alcohol, trifluoroethanol, allyl alcohol, heptafluorobutanol, pentafluoropropanol, pentafluorobutanol, nonafluorohexanol, various perfluoroalkylethanols, or combinations thereof, wherein the amount of said non-initiator solvent is less than about 5% by weight, and including said comonomer.

19. A monohydric polyfluorooxetane composition according to claim 18 , wherein said oligomer or polymer is said

wherein n is 1 to about 3, wherein R is methyl or ethyl, and wherein Rf contains from 1 to about 8 carbon atoms and has at least 85% of the non-carbon atoms being fluorine atoms, and wherein said comonomer is tetrahydrofuran.

20. A monohydric polyfluorooxetane oligomer or polymer composition according to claim 15 , wherein said composition contains an amount of cyclic oligomer which is less than about 8% by weight based upon the total weight of said polyfluorooxetane oligomer, polymer, or any copolymer produced.

21. A monohydric polyfluorooxetane oligomer composition according to claim 17 , wherein said composition contains an amount of cyclic oligomer which is less than about 8% by weight based upon the total weight of said polyfluorooxetane oligomer, polymer, or any copolymer produced.

22. A monohydric polyfluorooxetane oligomer composition according to claim 19 , wherein said composition contains an amount of cyclic oligomer which is less than about 2% or less by weight based upon the total weight of said polyfluorooxetane oligomer, polymer, or any copolymer produced.

23. A monohydric polyfluorooxetane oligomer composition, comprising:

a unit, derived from a fluorooxetane monomer, having the formula

where Dp is from about 2 to about 20, where each n is the same or different and independent is an integer from 1 to about 6, R is hydrogen or an alkyl of 1 to 6 carbon atoms, and each Rf is the same or different and independently on each repeat unit is a linear or branched fluorinated alkyl of 1 to 20 carbon atoms, a minimum of 75% of the non-carbon atoms of the alkyl being fluorine atoms and optionally the remaining non-carbon atoms being H, I, Cl, or Br,

said oligomer made by reacting a fluorooxetane monomer with a co-initiator solvent monoalcohol either free of a non-initiator solvent or in the presence of less than 10% by weight of a non-initiator solvent based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol, said fluorooxetane monomer having the formula

 where R, Rf, and n are as set forth herein above, and

optionally reacting said fluorooxetane monomer with at least one comonomer of an oxirane, a monomer having a 4-membered cyclic ether group (oxetane), a monomer having a 5-membered cyclic ether group, 1,4-dioxane, 1,3-dioxane, 1,3-dioxalane, trioxane, or caprolactone, or combinations thereof, in an amount of from about 0.1% to about 10% by weight based upon the total weight of said comonomer and said fluorooxetane monomer.

24. A monohydric polyfluorooxetane oligomer composition according to claim 23 , wherein said R 1 is derived from said co-initiator solvent monoalcohol comprising an organic alcohol, a polymeric alcohol, a tetrafluoroethylene based telomer fluoroalcohol, or combinations thereof, and

wherein said amount of said non-initiator solvent is less than about 5% by weight based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol.

25. A monohydric polyfluorooxetane oligomer composition according to claim 24 , wherein said organic alcohol has from 1 to 40 carbon atoms, wherein said polymeric alcohol contains repeat units derived from an alkylene oxide having from 2 to 6 carbon atoms and the number of repeat groups is from about 3 to about 30, and wherein said tetrafluoroethylene based telomer is CF 3 CF 2 (CF 2 CF 2 ) x CH 2 CH 2 OH where x is from 1 to about 19,

wherein said Dp is from about 2 to about 10, and

wherein each Rf is the same or different and independently is a linear or branched fluorinated alkyl having from 1 to about 15 carbon atoms, and including said comonomer and wherein said comonomer is tetrahydrofuran.

26. A monohydric polyfluorooxetane oligomer composition according to claim 25 , wherein said amount of said non-initiator solvent is less than about 3% by weight based upon the total weight of said non-initiator solvent and said co-initiator solvent monoalcohol.

Assignments (30)
RELEASE OF SECURITY INTEREST Recorded Apr 1, 2020
From: DEUTSCHE BANK AG NEW YORK BRANCH
To: OMNOVA SOLUTIONS INC.
Reel/Frame 052286/0911 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY COLLATERAL Recorded Apr 1, 2020
From: JPMORGAN CHASE BANK, N.A.
To: OMNOVA SOLUTIONS INC.
Reel/Frame 052286/0971 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT STATEMENT THAT THIS DOCUMENT SERVES AS AN OATH/DECLARATION PREVIOUSLY RECORDED AT REEL: 047383 FRAME: 0438. ASSIGNOR(S) HEREBY CONFIRMS THE TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS. Recorded Nov 5, 2018
From: KEYBANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 047422/0852 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Aug 31, 2018
From: KEYBANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 047383/0437 →
GRANT OF SECURITY INTEREST IN PATENTS Recorded Aug 3, 2018
From: AMPAC FINE CHEMICALS LLC
To: KEYBANK NATIONAL ASSOCIATION
Reel/Frame 046703/0605 →
NOTICE OF SUCCESSION OF AGENCY OF REEL/FRAME 019597/0227 Recorded Aug 29, 2016
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS SUCCESSOR AGENT
Reel/Frame 039851/0696 →
RELEASE OF SECURITY INTEREST Recorded Aug 5, 2016
From: U.S. BANK NATIONAL ASSOCIATION
To: AEROJET ROCKETDYNE, INC. (F/K/A AEROJET-GENERAL CORPORATION)
Reel/Frame 039594/0887 →
RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT R/F: 032365/0398 Recorded Dec 15, 2015
From: JEFFERIES FINANCE LLC, AS ADMINISTRATIVE AGENT
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 037300/0399 →
PATENT RELEASE AND REASSIGNMENT (R/F 029370/0835) Recorded Feb 27, 2014
From: KEYBANK NATIONAL ASSOCIATION, AS AGENT
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 032363/0222 →
SECURITY AGREEMENT Recorded Feb 27, 2014
From: AMPAC FINE CHEMICALS LLC
To: JEFFERIES FINANCE LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 032365/0398 →
SECURITY AGREEMENT Recorded Jun 21, 2013
From: AEROJET-GENERAL CORPORATION
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 030656/0667 →
COLLATERAL ASSIGNMENT AND SECURITY INTEREST OF PATENTS Recorded Nov 28, 2012
From: AMPAC FINE CHEMICALS LLC
To: KEYBANK NATIONAL ASSOCIATION
Reel/Frame 029370/0835 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE FROM AMERICAN FINE CHEMICALS LLC TO AMPAC FINE CHEMICALS LLC PREVIOUSLY RECORDED ON REEL 029203 FRAME 0091. ASSIGNOR(S) HEREBY CONFIRMS THE RELEASE BY SECURED PARTY. Recorded Nov 5, 2012
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 029245/0597 →
RELEASE OF SECURITY INTEREST Recorded Oct 26, 2012
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: AMERICAN FINE CHEMICALS LLC
Reel/Frame 029203/0091 →
SECURITY AGREEMENT Recorded Feb 2, 2011
From: AMPAC FINE CHEMICALS LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 025732/0985 →
RELEASE OF SECURITY INTEREST Recorded Jan 28, 2011
From: WELLS FARGO BANK, NATIONAL ASSOCIATION; WACHOVIA BANK, NATIONAL ASSOCIATION
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 025715/0485 →
GRANT OF SECURITY INTEREST IN CERTAIN PATENTS AND TRADEMARKS Recorded Jul 24, 2007
From: OMNOVA SOLUTIONS INC.
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 019597/0227 →
SECURITY AGREEMENT Recorded May 30, 2007
From: OMNOVA SOLUTIONS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 019353/0566 →
NOTICE OF GRANT OF SECURITY INTEREST Recorded Mar 15, 2007
From: AMPAC FINE CHEMICALS LLC
To: WACHOVIA BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 019009/0748 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2006
From: AEROJET FINE CHEMICALS LLC
To: AEROJET-GENERAL CORPORATION
Reel/Frame 017636/0396 →
NOTICE OF GRANT OF SECURITY INTEREST Recorded Apr 12, 2006
From: AMPAC FINE CHEMICALS LLC
To: WACHOVIA BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT AND CONTROL AGENT
Reel/Frame 017458/0506 →
NOTICE OF GRANT OF SECURITY INTEREST Recorded Apr 11, 2006
From: AMPAC FINE CHEMICALS LLC
To: WACHOVIA BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT AND CONTROL AGENT
Reel/Frame 017448/0842 →
CORRECTED NOTICE OF RECORDATION DOCUMENT ID NO. 700247361 Recorded Apr 10, 2006
From: GENCORP INC.
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 017458/0683 →
CORRECTION OF ASSIGNMENT DOCUMENT PREVIOUSLY RECORDED AT REEL/FRAME 017073/0162 Recorded Apr 3, 2006
From: AEROJET FINE CHEMICALS LLC
To: AEROJET-GENERAL CORPORATION
Reel/Frame 017422/0361 →
CORRECTION OF ASSIGNMENT DOCUMENT PREVIOUSLY RECORDED AT REEL/FRAME 017073/0175 Recorded Mar 1, 2006
From: AEROJET-GENERAL CORPORATION
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 017297/0756 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2005
From: AEROJET FINE CHEMICALS LLC
To: AEROJET-GENERAL CORPORATION
Reel/Frame 017073/0162 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2005
From: AEROJET-GENERAL CORPORATION
To: AMPAC FINE CHEMICALS LLC
Reel/Frame 017073/0175 →
SECURITY INTEREST Recorded Jun 17, 2003
From: OMNOVA SOLUTIONS, INC.
To: BANK ONE, NA, AS AGENT
Reel/Frame 014137/0401 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2001
From: MEDSKER, ROBERT; JIALANELLA, GARY L.; WEINERT, RAYMOND J.; GARCIA, GUILLERMINA C.
To: OMNOVA SOLUTIONS INC.
Reel/Frame 011628/0633 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2001
From: MALIK, ASLAM; CARLSON, ROLAND
To: AEROJET-GENERAL CORPORATION
Reel/Frame 011622/0899 →
Continuity (2)
Continuation In Part 0947351800 · Dec 28, 1999
Related Publication 20030208015A1 · Nov 6, 2003