IP Library Granted Patent US 7,354,985
Granted Patent B2
US 7,354,985 · App. 10/678,663 · Granted Apr 8, 2008

Fluorinated thermoset polyurethane elastomers prepared from polyether prepolymers formed from mono-substituted fluorinated oxetane monomers

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Quick Facts
Patent No.
US 7,354,985
App. No.
10/678,663
Granted
Apr 8, 2008
Kind
B2
Abstract

This application is directed to novel fluorinated polymers and prepolymers derived from mono-substituted oxetane monomers having fluorinated alkoxymethylene side-chains and the method of making these compositions. The mono-substituted fluorinated oxetane monomers having fluorinated alkoxymethylene side-chains are prepared in high yield by the reaction of a fluorinated alkoxides with either 3-halomethyl-3-methyloxetane premonomers or aryl sulfonate derivative of 3-hydroxymethyl-3-methyloxetane premonomers. Preparation of a mono-substituted 3-bromomethyl-3-methyloxetane premonomer via a simple, high yield process amenable to commercial scaleup is also disclosed. The fluorinated oxetane monomers of this invention can be readily homo/co-polymerized in the presence of a Lewis acid and polyhydroxy compounds to obtain hydroxy-terminated polyether prepolymers having fluorinated alkoxymethylene side chains. Additionally, the fluorinated oxetane monomers can be copolymerized with non-fluorinated monomers such as tetrahydrofuran to give polyether prepolymers with improved hydrocarbon compatibility. These prepolymers are polydisperse and exhibit number average molecular weights from 5,000 to about 50,000. These prepolymers are amorphous oils with primary hydroxy end-groups and thus function efficiently as the soft block for the synthesis of a variety of thermoset/thermoplastic elastomers and plastics having the characteristics of very low surface energy, high hydrophobicity, low glasss transition temperature and low coefficient of friction. The polyurethanes derived from the prepolymers of this invention are elastomeric and, in addition to the above characteristics, exhibit high moisture resistance, high tear strength and excellent adhesion to a variety of substrates.

Claims (33)

1. A fluorinated thermoset polyurethane elastomer represented by the formula (I):

comprising a polyether segment; a polyisocyanate unit covalently bonded to the polyether segment; and a cross-link formed from a cross-linking agent,

wherein:

n is from 1-3;

R is independently selected from the group consisting of methyl and ethyl;

R f is independently selected from the group consisting of perfluorinated alkyls having from 1 to about 20 carbons and oxa-perfluorinated polyethers having from about 4 to about 20 carbons;

X is a variable integer from about 10 to about 250;

Z is a variable integer from 2 to about 50

R 1 is a divalent hydrocarbyl radical;

A is an end-group selected from the group consisting of H and an isocyanate fragment; and

B is an end-group selected from the group consisting of a fragment having an OH and an isocyanate fragment.

2. The fluorinated thermoset polyurethane elastomer of claim 1 , wherein the cross-linking agent is selected from the group consisting of a low molecular weight polyol and a low molecular weight polyamine.

3. The fluorinated thermoset polyurethane elastomer of claim 1 , wherein the crosslinking agent is selected from the group consisting of trimethylolpropane, pentaerythitol, trimethylolethane, triethanolamine, 1,4-butanediamine, xylene diamine, diethylenetriamine, methylene dianiline, diethanolamine and combinations thereof.

4. The fluorinated thermoset polyurethane elastomer of claim 1 , wherein the polyether segment is produced from at least one monomer selected from the group consisting of 3-(2,2,3,3,4,4,5-heptafluorobutoxymethyl)-3-methyloxetane; 3-(2,2,2-trifluoroethoxymethyl)-3-methyloxetane; 3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyloxymethyl)-3-methyloxetane; 3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorooctyloxymethyl)-3-methyloxetane; and 3-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-heneicosa-fluorododecyloxymethyl)-3-methyloxetane.

5. The fluorinated thermoset polyurethane elastomer of claim 1 , wherein the polyisocyanate unit is produced from an isocyanate selected from the group consisting of hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), 4,4′-methylene diphenylisocyanate (MDI), polymeric MDI (Isonate®), toluene diisocyanates, saturated MDI (HMDI), polymeric HDI (Desmodur® N-100 and N-3200), trimethylhexane diisocyanate and combinations thereof.

6. A method of making a fluorinated thermoset polyurethane elastomer, comprising the steps of:

a) mixing a prepolymer with an isocyanate, a cross-linking agent, and a catalyst to form a reaction mixture, wherein the prepolymer is produced from a monomer selected from the group consisting of FOX (fluorinated OXetane) and FOX/THF (tetrahydrofuran); and

b) curing the reaction mixture to form the thermoset polyurethane elastomer.

7. The method of claim 6 , further comprising the steps of casting the reaction mixture into a mold; and degassing the cast reaction mixture after step a).

8. The method of claim 6 , wherein the mixture is cured at a temperature between about 20° C. to about 150° C.

9. The method of claim 6 , wherein the reaction mixture is heated to about 65° C. for about 3 to about 16 hours.

10. The method of claim 6 , wherein the isocyanate is selected from the group consisting of hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), 4,4′-methylene diphenylisocyanate (MDI), polymeric MDI (Isonate®), toluene diisocyanates, saturated MDI (HMDI), polymeric HDI (Desmodur® N-100 and N-3200), trimethylhexane diisocyanate and combinations thereof.

11. The method of claim 6 , wherein the cross-linking agent is selected from the group consisting of a low molecular weight polyol and a low molecular weight polyamine.

12. The method of claim 6 , wherein said crosslinking agent is selected from the group consisting of trimethylolpropane, pentaerythitol, trimethylolethane, triethanolamine, 1,4-butanediamine, xylene diamine, diethylenetriamine, methylene dianiline, diethanolamine and combinations thereof.

13. The method of claim 6 , wherein the catalyst is a member selected from the group consisting of dibutyltin dilaurate, triethyamine, triethylene diamine, triphenyl bismuth, chromium acetylacetonate, lead octonate, ferric acetylacetonate, tin octanoate and combinations thereof.

14. The fluorinated thermoset polyurethane elastomer of claim 2 , wherein the crosslinking agent is a low molecular weight polyamine.

15. The fluorinated thermoset polyurethane elastomer of claim 3 , wherein the crosslinking agent is methylene dianiline.

16. The fluorinated thermoset polyurethane elastomer of claim 3 , wherein the crosslinking agent is trimethylolpropane.

17. The fluorinated thermoset polyurethane elastomer of claim 5 , wherein the isocyanate is selected from the group consisting of polymeric HDI (Desmodur® N-100) and polymeric HDI (Desmodur® N-3200).

18. The fluorinated thermoset polyurethane elastomer of claim 5 , wherein the isocyanate is isophorone diisocyanate (IPDI).

19. The fluorinated thermoset polyurethane elastomer of claim 5 , wherein the isocyanate is selected from the group consisting of saturated MDI (HMDI) and polymeric MDI (Isonate®).

20. The method of claim 11 , wherein the crosslinking agent is a low molecular weight polyamine.

21. The method of claim 13 , wherein the catalyst is dibutyltin dilaurate.

Assignments (22)
RELEASE OF SECURITY INTEREST Recorded Aug 5, 2016
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To: AEROJET ROCKETDYNE, INC. (F/K/A AEROJET-GENERAL CORPORATION)
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PATENT RELEASE AND REASSIGNMENT (R/F 029370/0835) Recorded Feb 27, 2014
From: KEYBANK NATIONAL ASSOCIATION, AS AGENT
To: AMPAC FINE CHEMICALS LLC
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From: AMPAC FINE CHEMICALS LLC
To: JEFFERIES FINANCE LLC, AS ADMINISTRATIVE AGENT
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SECURITY AGREEMENT Recorded Jun 21, 2013
From: AEROJET-GENERAL CORPORATION
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COLLATERAL ASSIGNMENT AND SECURITY INTEREST OF PATENTS Recorded Nov 28, 2012
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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
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From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: AMERICAN FINE CHEMICALS LLC
Reel/Frame 029203/0091 →
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From: AMPAC FINE CHEMICALS LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS AGENT
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RELEASE OF SECURITY INTEREST Recorded Jan 28, 2011
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NOTICE OF GRANT OF SECURITY INTEREST Recorded Apr 12, 2006
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