Peroxide curable fluoropolymers obtainable by polymerization with non-fluorinated emulsifiers

Patent metadata

Field	Value
Publication number	US-10875948-B2
Application number	US-201615553101-A
Country	US
Kind code	B2
Filing date	Feb 22, 2016
Priority date	Feb 23, 2015
Publication date	Dec 29, 2020
Grant date	Dec 29, 2020

Abstract

Curable fluoropolymer containing repeating units derived from VDF and TFE and at least one other fluorinated comonomer and further containing —CF2CH2I end groups and branching sites derived from one or more perfluorinated bisolefinic ether(s) used as modifier(s), wherein the one or more perfluorinated bisolefinic ether(s) used as modifier(s) correspond to the general formula: CF2═CF—(CF2)n—O—(R1)—O—(CF2)mCF═CF2 wherein n and m are independent from each other either 1 or 0 and wherein R1 represents a perfluorinated linear or branched, cyclic or acyclic aliphatic or aromatic hydrocarbon residue that may be interrupted by one or more oxygen atoms and comprises up to 30 carbon atoms. Further provided are methods of making the curable fluoropolymers and for making an article containing the curable polymers.

First claim

The invention claimed is:

1. A curable fluoropolymer containing repeating units derived from vinylidene fluoride (VDF) and tetrafluoroethylene (TFE) and at least one other fluorinated comonomer and further containing (i) —CF 2 CH 2 I end groups and (ii) branching sites derived from one or more perfluorinated bisolefinic ether modifier;
wherein the polymer is obtained by an aqueous emulsion polymerization comprising the addition of one or more non-fluorinated emulsifier but wherein essentially no fluorinated emulsifier is added; and
wherein the one or more perfluorinated bisolefinic ether modifier correspond to the general formula:
CF 2 ═CF—(CF 2 ) n —O—(R f )—O—(CF 2 ) m —CF═CF 2

wherein n and m are independent from each other either 1 or 0 and wherein R f represents a perfluorinated linear or branched, cyclic or acyclic aliphatic or aromatic hydrocarbon residue that may be interrupted by one or more oxygen atoms and comprises up to 30 carbon atoms.

2. The curable fluoropolymer of claim 1 having a molar —CH 2 I to —CH 2 OH ratio of at least 30.

3. The curable fluoropolymer of claim 1 wherein a seed composition is used for the aqueous emulsion polymerization to produce the curable fluoropolymer and wherein the seed composition is obtained by aqueous emulsion polymerization of fluorinated monomers and wherein the non-fluorinated emulsifier is added to prepare the seed composition.

4. The curable fluoropolymer according to claim 1 , wherein the amount of the perfluorinated bisolefinic ether modifiers used is less than 0.95% by weight based on the total weight of the monomers.

5. The curable fluoropolymer according to claim 1 , wherein the modifiers are selected from ethers according to the general formula:
CF 2 ═CF—(CF 2 ) n —O—(CF 2 ) p —O—(CF 2 ) m —CF═CF 2

wherein n and m are independent from each other either 1 or 0 and p is an integer from 1 to 10.

6. The curable fluoropolymer according to claim 1 , wherein the modifiers are selected from ethers according to the general formula:
CF 2 ═CF—(CF 2 ) n —O—(CF 2 ) p —O—(CF 2 ) m —CF═CF 2

wherein n and m are independent from each other either 1 or 0 and p is an integer selected from 3, 5 and 7.

7. The curable fluoropolymer according to claim 1 , further having a compression set (ASTM 395, method B) of less than 25% after press curing at 40 bar and 177° C. for 7 minutes and post curing at 230° C. for 2 hours.

8. The curable fluoropolymer according to claim 1 , having less than 4.0 wt % of extractable material after curing based on the total amount of cured polymer subjected to extraction.

9. The curable fluoropolymer according to claim 1 , further having units derived from a cure site monomer selected from fluorinated iodo-olefins of the general formula:
Z′—R f —CX═CX 2

wherein each X independently represents H or F, preferably H, Z′ is I, Rf is a C 1 -C 12 fluoro- or perfluoroalkylene, which optionally may be interrupted by one or more than one ether atom, optionally containing chlorine atoms and/or ether atoms.

10. A curable fluoropolymer containing repeating units derived from vinylidene fluoride (VDF) and tetrafluoroethylene (TFE) and at least one other fluorinated comonomer and further containing (i) —CF 2 CH 2 I end groups and (ii) branching sites derived from one or more perfluorinated bisolefinic ether modifier;
wherein the polymer is obtained by an aqueous emulsion polymerization comprising the addition of one or more non-fluorinated emulsifier but wherein essentially no fluorinated emulsifier is added; and
wherein the one or more perfluorinated bisolefinic ether modifier correspond to the general formula:
CF 2 ═CF—(CF 2 ) n —O—(R f )—O—(CF 2 ) m —CF═CF 2

wherein n and m are independent from each other either 1 or 0 and wherein R f represents a perfluorinated linear or branched, cyclic or acyclic aliphatic or aromatic hydrocarbon residue that may be interrupted by one or more oxygen atoms and comprises up to 30 carbon atoms, the curable fluoropolymer further having units derived from a cure site monomer selected from the general formula:
R f —CF(I)—(CX 2 ) n —(CX 2 CXR) m —O—R″ f —O k —(CXR′CX 2 ) p —(CX 2 ) q —CF(I)—R′ f

wherein X is independently selected from F, H, and Cl; R f and R′ f are independently selected from F and a monovalent perfluoroalkane having 1-3 carbons; R is F, or a partially fluorinated or perfluorinated alkane comprising 1-3 carbons; R″ f is a divalent fluoroalkylene having 1-5 carbons or a divalent fluorinated alkylene ether having 1-8 carbons and at least one ether linkage; k is 0 or 1; and n, m, and p are independently selected from an integer from 0-5, wherein, n plus m is at least 1 and p plus q is at least 1.

11. The curable fluoropolymer according to claim 1 , further having a reduced viscosity of from 20 mL/g to about 180 mL/g.

12. The curable fluoropolymer according to claim 3 , wherein the seed composition is obtained by the aqueous emulsion polymerization involving polymerizing fluorinated monomers in the presence of one or more non-fluorinated saturated emulsifiers and wherein the monomers are selected from VDF, TFE and at least one other fluorinated comonomer.

13. The curable fluoropolymer according to claim 1 , wherein the non-fluorinated emulsifiers are selected from aliphatic hydrocarbon sulfate or sulfonate emulsifiers, wherein the hydrocarbon part contains one or more oxygen containing moieties and wherein the sulfate or sulfonate emulsifiers may contain one or more than one sulfate or sulfonate groups.

14. The curable fluoropolymer according to claim 1 , wherein the non-fluorinated emulsifiers are selected from aliphatic hydrocarbon sulfate or sulfonate emulsifiers, wherein the sulfate or sulfonate emulsifiers may contain one or more than one sulfate or sulfonate groups and wherein the hydrocarbon part contains one or more oxygen containing moieties selected from alkyl ether groups, poly ether alkyl groups, carboxylate ester (—O—C(═O)—) groups, carboxamide (—NYX—C(═O)— groups and combinations thereof, wherein Y and X may be H, or an alkyl group and combinations thereof.

15. The curable fluoropolymer according to claim 1 , wherein the non-fluorinated emulsifier is selected from hydrocarbon sulfates or sulfonates wherein the hydrocarbon part may be substituted by one or more catenary oxygen atoms.

16. A cured composition obtained after subjecting the curable fluoropolymer according to claim 1 , to a curing reaction.

17. An article comprising the cured composition of claim 16 .

18. Method of making an article comprising subjecting the curable polymer composition according to claim 1 , to curing and shaping wherein the shaping may occur after or during the curing.

19. Method of making a curable fluoropolymer comprising i) polymerizing VDF, TFE and at least one other comonomer in an aqueous emulsion polymerization in the absence of any added fluorinated emulsifiers but in the presence of a non-fluorinated emulsifier, an iodine-containing chain transfer agent (CTA), one or more perfluorinated bisolefinic ether modifier(s) and, optionally, one or more iodine-containing cures site monomers, wherein the iodine-containing CTA is selected from fluorinated iodo-olefins wherein the olefin chain may be interrupted once or more than once by an ether oxygen, and wherein the modifier is selected from perfluorinated bisolefinic ether modifiers corresponding to the general formula:
CF 2 ═CF—(CF 2 ) n —O—(R f )—O—(CF 2 ) m —CF═CF 2

wherein n and m are independent

Assignees

• 3M Innovative Properties Co

Inventors

• Jochum Florian D
• Hintzer Klaus
• Lochhaas Kai Helmut
• Kaspar Harald
• Zipplies Tilman C
• Traunspurger Helmut

Classifications

• C08F259/08

  on to polymers containing fluorine · CPC title

• C08F216/125

  Monomers containing two or more unsaturated aliphatic radicals, e.g. trimethylolpropane triallyl ether or pentaerythritol triallyl ether · CPC title

• C08F214/26

  Tetrafluoroethene · CPC title

• C08F214/222 Primary

  with fluorinated vinyl ethers · CPC title

• C08F2/22

  Emulsion polymerisation · CPC title