IP Library Granted Patent US 6,972,317
Granted Patent B2
US 6,972,317 · App. 10/108,916 · Granted Dec 6, 2005

Monohydric polyfluorooxetane polymer and radiation curable coatings containing a monofunctional polyfluorooxetane polymer

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Quick Facts
Patent No.
US 6,972,317
App. No.
10/108,916
Granted
Dec 6, 2005
Kind
B2
Abstract

Monofunctional polyfluorooxetane oligomers and polymers are prepared by the cationic polymerization of fluorooxetane monomers with a monoalcohol. The fluorooxetane oligomers or polymers can be copolymerized with generally cyclic ethers. Alternatively, the polyfluorooxetane oligomer or polymer 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 that have previously been provided by migratory chemicals such as waxes and oils. The partially or fully fluorinated side groups of the fluorooxetanes are believed to be disproportionately present at the interfaces between the coating and the substrate and between the coating and the atmosphere.

Claims (14)

1. A process for forming a partially fluorinated functionalized oligomer or polymer comprising:

reacting a partially fluorinated monohydric polyoxetane containing alcohol, optionally including non-oxetane repeating units, either a) sequentially with a di or polyisocyanate forming an isocyanate terminated oligomer or polymer and then reacting said isocyanate terminated oligomer or polymer with a functionalizing compound forming a functionalized polyoxetane oligomer, or polymer or b) in a single step with an isocyanate functionalized compound and forming a functionalized polyoxetane oligomer or polymer.

2. A process according to claim 1 wherein said monohydric polyoxetane containing alcohol comprises repeating units of the formula

or combinations thereof, where n is the same or different and independently is an integer between 1 and 5, 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; or each Rf is the same or different and independently is an oxaperfluorinated polyether having from 4 to 60 carbon atoms, and

wherein said functionalized group is an acrylate, a methacrylate, an allylic, a melamine, an amine, an acetylacetate, an epoxide, a silyl, or an isocyanate, or combinations thereof.

3. A process according to claim 2 , wherein said monohydric polyoxetane containing alcohol is reacted with a diisocyanate forming said isocyanate terminated polyoxetane oligomer or polymer which is then reacted with said functionalizing compound.

4. A process according to claim 1 , wherein said repeat group is said

5. A process for forming a partially fluorinated functionized oligomer or polymer comprising;

reacting a partially fluorinated polyoxetane containing monohydric alcohol, optionally including non-oxetane repeating units either a) sequentially with a di or polyepoxy compound forming an epoxy terminated oligomer or polymer and then reacting that epoxy terminated oligomer or polymer with a functionalizing compound forming functionalized polyoxetane oligomer or polymer, or b) in a single step reacting said monohydric alcohol with an epoxy functionalized compound and forming an functionized polyoxetane oligomer or polymer.

6. A process according to claim 5 , wherein said monohydric polyoxetane containing alcohol comprises repeating units of the formula

or combinations thereof, where n is the same or different and independently is an integer between 1 and 5, 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; or each Rf is the same or different and independently is an oxaperfluorinated polyether having from 4 to 60 carbon atoms, and

wherein said functionalized group is an acrylate, a methacrylate, an allylic, a melamine, an amine, an acetylacetate, an epoxide, a silyl, or an isocyanate, or combinations thereof.

7. A process according to claim 6 , wherein said monohydric polyoxertane containing alcohol is reacted with a diepoxy forming said isocyanate terminated polyoxetane oligomer or polymer which is then reacted with said functionalizing compound.

8. A process according to claim 5 , wherein said repeat unit is said

Assignments (15)
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 025495/0754 Recorded Aug 29, 2016
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS SUCCESSOR AGENT
Reel/Frame 039851/0553 →
SECURITY INTEREST Recorded Aug 26, 2016
From: OMNOVA SOLUTIONS INC.
To: JPMORGAN CHASE BANK, N.A., AS AGENT
Reel/Frame 039555/0403 →
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 →